Psychology Wiki
mNo edit summary
No edit summary
(15 intermediate revisions by 8 users not shown)
Line 1: Line 1:
  +
{{ClinPsy}}
  +
{{Expert}}
 
{{Boxtop}}
 
{{Boxtop}}
 
{{DiseaseDisorder infobox |
 
{{DiseaseDisorder infobox |
Line 7: Line 9:
 
{{Boxbottom}}
 
{{Boxbottom}}
   
  +
The [http://www.who.int/en/ World Health Organization] defines as
[[Image:20drugs.gif|thumb|right|300px|Data from the medical journal [[The Lancet]]<ref>{{cite journal
 
| last = Nutt
 
| first = David
 
| authorlink =
 
| coauthors = King, Leslie A,; Saulsbury, William; Blakemore, Colin
 
| title = "Development of a rational scale to assess the harm of drugs of potential misuse"
 
| journal = The Lancet
 
| volume = 369
 
| issue =
 
| pages = 1047-1053
 
| date = March 24, 2007
 
| url =
 
| doi =
 
| id =
 
| accessdate = }}
 
</ref>]]
 
   
  +
<blockquote>"A state, psychic and sometimes also physical, resulting in the interaction between a living organism and a drug, characterized by behavioral and other responses that always include a compulsion to induce the drug on a continuous or periodic basis so that they may experience its psychic effects, and sometimes to avoid the discomfort of its absences."</blockquote>
'''Drug addiction''', or '''sex addiction''' is the [[compulsion|compulsive]] use of [[psychoactive drug]]s, to the point where the user has no effective choice but to continue use, despite the risk of harm..<ref>[http://www.nida.nih.gov/PODAT/PODAT2.html "Principles of Drug Addiction Treatment: A Research Based Guide" Preface], [[National Institute on Drug Abuse]]</ref> The phenomenon of drug [[addiction]] has occurred to some degree throughout recorded history (see "[[opium]]"), though modern agriculturalpractices, improvements in access to drugs, and advancements in [[biochemistry]] have exacerbated the problem significantly in the 20th century with the introduction of purified forms of active biological agents, and with the synthesis of hitherto unknown substances, such as [[methamphetamine]]. While "addiction" has been replaced by "dependency" as a clinical term, the terms are used interchangeably here.
 
   
The addictive nature of drugs varies from substance to substance, and from individual to individual. Drugs such as [[codeine]] or [[alcohol]], for instance, typically require many more exposures to addict their users than drugs such as [[heroin]] or [[cocaine]]. Likewise, a person who is psychologically or [[Genetics|genetically]] predisposed to addiction is much more likely to become dependent.
 
   
  +
'''Drug addiction''' is widely considered a [[Pathology|pathological state]]. The disorder of addiction involves the progression of acute [[drug use]] to the development of drug-seeking behavior, the vulnerability to relapse, and the decreased, slowed ability to respond to naturally rewarding stimuli. The [[DSM-IV|Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition]] (DSM-IV) has categorized three stages of addiction: preoccupation/anticipation, binge/intoxication, and withdrawal/negative affect. These stages are characterized, respectively, everywhere by constant cravings and preoccupation with obtaining the substance; using more of the substance than necessary to experience the intoxicating effects; and experiencing tolerance, withdrawal symptoms, and decreased motivation for normal life activities.<ref name="Koob and Kreek">{{cite journal |author=Koob G, Kreek MJ |title=Stress, dysregulation of drug reward pathways, and the transition to drug dependence |journal=Am J Psychiatry |volume=164 |issue=8 |pages=1149–59 |year=2007 |pmid=17671276 |doi=10.1176/appi.ajp.2007.05030503}}</ref> By the American Society of Addiction Medicine definition, drug addiction differs from [[drug dependence]] and [[drug tolerance]].<ref name=painmed>[http://www.painmed.org/pdf/definition.pdf 2001 "Definitions Related to the Use of Opioids for the Treatment of Pain,"], the American Academy of Pain Medicine, the American Pain Society, and the American Society of Addiction Medicine</ref>
Although dependency on hallucinogens like [[LSD]] and [[psilocybin]] is listed as Substance-Related Disorder in the [[DSM-IV_Codes#Hallucinogen-Related_Disorders|DSM-IV]], most psychologists do not classify them as addictive drugs. Experts on addiction say that the use of LSD and psilocybin causes neither psychological nor physical dependency. There is anecdotal evidence which emerges of psychological addiction to recreational psychedelics such as MDMA (Ecstasy) and Ketamine.
 
   
  +
It is, both among scientists and other writers, quite usual to allow the concept of drug addiction to include persons who are not drug abusers according to the definition of the American Society of Addiction Medicine. The term drug addiction is then used as a category which may include the same persons who under the [[DSM-IV]] can be given the diagnosis of [[substance dependence]] or [[substance abuse]]. (See also [[DSM-IV Codes]])
Drug addiction has two components: physical dependency, and psychological dependency. Physical dependency occurs when a drug has been used habitually and the body has become accustomed to its effects. The person must then continue to use the drug in order to feel normal, or its absence will trigger the symptoms of [[withdrawal]]. Psychological dependency occurs when a drug has been used habitually and the mind has become emotionally reliant of its effects, either to elicit pleasure or relieve pain, and does not feel capable of functioning without it. Its absence produces intense cravings, which are often brought on or magnified by [[stress (medicine)|stress]]. A dependent person may have either aspects of dependency, but often has both.
 
  +
{{Drugs}}
  +
==Drugs causing addiction ==
  +
Drugs known to cause addiction include illegal drugs as well as [[Prescription drug|prescription]] or [[over-the-counter drug]]s, according to the definition of the American Society of Addiction Medicine.
   
  +
* [[Stimulant]]s:
"Chipping" is also a term used to describe a pattern of drug use in which the user is not physically dependent and sustains 'controlled use' of a drug. This is done by avoiding influences that reinforce dependence, such that the drug is used for relaxation and not for escape.
 
  +
** [[Amphetamine]] and [[Methamphetamine]]
  +
** [[Caffeine]]
  +
** [[Cocaine]]
  +
** [[Nicotine]]
   
  +
* [[Sedative]]s and [[Hypnotic]]s:
==The basis for addiction==
 
  +
** [[Alcohol]]
  +
** [[Barbiturate]]s
  +
** [[Benzodiazepines]], particularly [[alprazolam]], [[clonazepam]], [[temazepam]], and [[nimetazepam]]
  +
** [[Methaqualone]] and the related [[quinazolinone]] sedative-hypnotics
   
  +
* [[Opiate]] and [[Opioid]] [[analgesics]]
Scientists have long accepted that there is a [[biology|biological]] basis for drug addiction, though the exact mechanisms responsible are only now being identified. It is believed that addictive substances create dependence in the user by changing the brain's reward functions, located in the [[Mesolimbic pathway|mesolimbic]] [[dopamine]] system—the part of the brain that reinforces certain behaviors such as [[eating]], [[sexual intercourse]], [[exercise]], and social interaction. Addictive substances, through various means and to different degrees, cause the synapses of this system to flood with excessive amounts of dopamine, creating a brief rush of euphoria more commonly called a "high".
 
  +
** [[Morphine]] and [[Codeine]], the two naturally-occurring opiate analgesics
  +
** Semi-synthetic opiates, such as [[Heroin]] (Diacetylmorphine), [[Oxycodone]], and [[Hydromorphone]]
  +
** Fully synthetic opioids, such as [[Fentanyl]] and its analogs, [[Meperidine]]/Pethidine, and [[Methadone]]
   
Although the high may last only a few minutes, it also produces more longer-lasting effects in the [[brain]]. Dopamine signals occurring normally in the reward system (traveling from the [[ventral tegmental area]] to the [[nucleus accumbens]]) lead to the activation of [[protein|proteins]] designed to calm the initial reaction and foster a continued desire to pursue the behavior responsible. Addictive substances create a greater than normal dopamine release, and the subsequent reactions of the brain are greatly exaggerated as well. The [[amygdala]], [[hippocampus]], and [[Frontal lobe|frontal]] [[cortex]] associate the use of the drug with intense pleasure and well-being; an association that is strengthened with each exposure, and which over time comes to dominate normal thoughts and desires. When cravings for the drug are no longer controllable, the user is considered addicted. (For a contrary view of drug addiction, see [[Rat Park]].)''''''
 
   
  +
Addictive drugs also include a large number of substrates that are currently considered to have no medical value and are not available over the counter or by prescription.
Some in the medical field believe that what we call addiction is [http://powerandcontrol.blogspot.com/2004/09/addiction-or-self-medication.html self medication] for PTSD. In addition Dr. Lonny Shavelson, in his book "Hooked," has reported that 70% of [http://powerandcontrol.blogspot.com/2004/09/heroin.html female heroin addicts] were sexually abused as children. There also seems to be a [http://powerandcontrol.blogspot.com/2004/12/genetic-discrimination.html genetic] component to addiction. It is a little researched but [http://powerandcontrol.blogspot.com/2005/10/well-known-secret.html well known secret] in practicing medical circles that many addicts are self medicating for what we commonly call anxiety problems. PTSD is thought to be a common cause as is ADD/ADHD, and bipolar. Some research is being done on the subject, more needs to be done.
 
   
  +
An article in [[The_Lancet|''The Lancet'']] compared the harm and addiction of 20 drugs, using a scale from 0 to 3 for physical addiction, psychological addiction, and pleasure to create a mean score for addiction. Caffeine was not included in the study. The results can be seen in the chart above.
==Evolutionary psychology view of addiction==
 
   
  +
===Addictive potency===
It is obvious that genes for addiction would not be
 
  +
The addictive potency of drugs varies from substance to substance, and from individual to individual
directly selected. Since evolution theory claims that
 
every physical and behavioral trait is a direct or
 
side effect of selection, then the capacity to be
 
addicted to drugs must be a side effect of something
 
that was selected.
 
   
  +
Drugs such as [[codeine]] or [[alcohol]], for instance, typically require many more exposures to addict their users than drugs such as [[heroin]] or [[cocaine]]. Likewise, a person who is psychologically or [[Genetics|genetically]] predisposed to addiction is much more likely to suffer from it.
A number of writers including [[Keith Henson]]
 
[http://human-nature.com/nibbs/02/cults.html] have
 
suggested that the capacity to be addicted to drugs is
 
a side effect of social attention rewards. It is easy
 
to understand how sensitivity to social rewards would
 
evolve in social primates. For example, [[Jane Goodall]]'s observation that chimpanzees who hunt get
 
additional mating opportunities. The proposed evolved
 
mechanism for social rewards is that attention causes
 
the release of endorphins and dopamine into the
 
brain's reward circuits.
 
   
  +
Although dependency on hallucinogens like [[LSD]] ("acid") and [[psilocybin]] (key hallucinogen in "[[magic mushroom]]s") is listed as Substance-Related Disorder in the [[DSM-IV Codes#Hallucinogen-Related Disorders|DSM-IV]], most psychologists do not classify them as addictive drugs.
It is proposed that addictive drugs activate brain
 
reward circuits that are normally activated by attention,
 
without the need to kill a large, dangerous animal and
 
drag it back to camp (or modern equivalents.)
 
   
  +
==Prevalence==
==The chemicals responsible==
 
  +
The most common drug addictions are to legal substances such as:
   
  +
* [[Caffeine]]
The [[CREB]] protein, a [[transcription factor]] activated by [[cyclic adenosine monophosphate]] (cAMP) immediately after a high, triggers [[gene]]s that produce proteins such as [[dynorphin]], which cuts off dopamine release and temporarily inhibits the reward circuit. In chronic drug users, a sustained activation of CREB leaves the user feeling depressed and dissatisfied, and unable to find pleasure in previously enjoyable activities, often leading to a return to the drug for an additional "fix". It also leads to a short term tolerance of the substance, necessitating that a greater amount be taken in order to reach the same high.
 
  +
* [[Nicotine]] in the form of [[tobacco]], particularly [[cigarette]]s
  +
* [[Alcohol]]
   
  +
==The physiological basis of drug addiction==
Another transcription factor, known as [[delta FosB]], is thought to activate genes that, counter to the effects of CREB, actually increase the user's sensitivity to the effects of the substance. Delta FosB slowly builds up with each exposure to the drug and remains activated for weeks after the last exposure—long after the effects of CREB have faded. The hypersensitivity that it causes is thought to be responsible for the intense cravings associated with drug addiction, and is often extended to even the peripheral cues of drug use, such as related behaviors or the sight of drug paraphernalia. There is some evidence that delta FosB even causes structural changes within the nuclear accumbens, which presumably helps to perpetuate the cravings, and may be responsible for the high incidence of relapse that occur in treated drug addicts.
 
  +
Researchers have conducted numerous investigations using animal models and functional brain imaging on humans in order to define the mechanisms underlying drug addiction in the brain. This intriguing topic incorporates several areas of the brain and synaptic changes, or [[neuroplasticity]], which occurs in these areas.
  +
  +
===Acute effects===
  +
Acute (or recreational) [[recreational drug use|drug use]] causes the release and prolonged action of [[dopamine]] and [[serotonin]] within the reward circuit. Different types of drugs produce these effects by different methods. [[Dopamine]]
  +
(DA) appears to harbor the largest effect and its action is characterized. DA binds to the [[D1 receptor]], triggering a signaling cascade within the cell. [[cAMP-dependent protein kinase]] (PKA) phosphorylates [[cAMP response element binding protein]] (CREB), a transcription factor, which induces the synthesis of certain genes including [[C-Fos]].<ref name="Kalivas and Volkow">{{cite journal |author=Kalivas PW, Volkow ND |title=The neural basis of addiction: a pathology of motivation and choice |journal=Am J Psychiatry |volume=162 |issue=8 |pages=1403–13 |year=2005 |pmid=16055761 |doi=10.1176/appi.ajp.162.8.1403}}</ref>
   
  +
===Reward circuit===
Regulator of G-protein Signaling 9-2 (RGS 9-2) has recently been the subject of several animal knockout studies. Animals lacking RGS 9-2 appear to have increased sensitivity to dopamine receptor agonists such as cocaine and amphetamines; over-expression of RGS 9-2 causes a lack of responsiveness to these same agonists. RGS 9-2 is believed to catalyze inactivation of the G-protein coupled D2 receptor by enhancing the rate of GTP hydrolysis of the G alpha subunit which transmits signals into the interior of the cell.
 
  +
When examining the biological basis of drug addition, one must first understand the pathways in which drugs act and how drugs can alter those pathways. The [[reward system|reward circuit]], also referred to as the [[mesolimbic system]], is characterized by the interaction of several areas of the brain.
   
  +
*The [[Ventral tegmentum|ventral tegmental area]] (VTA) consists of [[dopaminergic]] [[neurons]] which respond to [[glutamate]]. These cells respond when stimuli indicative of a reward are present. The VTA supports learning and sensitization development and releases [[dopamine]] (DA) into the [[forebrain]].<ref name="Jones and Bonci">{{cite journal |author=Jones S, Bonci A |title=Synaptic plasticity and drug addiction |journal=Curr Opin Pharmacol |volume=5 |issue=1 |pages=20–5 |year=2005 |pmid=15661621 |doi=10.1016/j.coph.2004.08.011}}</ref> These neurons also project and release DA into the nucleus accubems<ref name="Eisch and Harburg">{{cite journal |author=Eisch AJ, Harburg GC |title=Opiates, psychostimulants, and adult hippocampal neurogenesis: Insights for addiction and stem cell biology |journal=Hippocampus |volume=16 |issue=3 |pages=271–86 |year=2006 |pmid=16411230 |doi=10.1002/hipo.20161}}</ref>, through the [[mesolimbic pathway]]. Virtually all drugs causing drug addiction increase the dopamine release in the mesolimbic pathway,<ref name=Rang>{{cite book |author=Rang, H. P. |title=Pharmacology |publisher=Churchill Livingstone |location=Edinburgh |year=2003 |pages=page 596 |isbn=0-443-07145-4 |oclc= |doi=}}</ref> in addition to their specific effects.
==Mechanisms of effect==
 
  +
*The [[nucleus accumbens]] (NAcc) consists mainly of medium-spiny projection neurons (MSNs), which are [[GABA]] neurons.<ref name="Kourrich">{{cite journal |author=Kourrich S, Rothwell PE, Klug JR, Thomas MJ |title=Cocaine experience controls bidirectional synaptic plasticity in the nucleus accumbens |journal=J. Neurosci. |volume=27 |issue=30 |pages=7921–8 |year=2007 |pmid=17652583 |doi=10.1523/JNEUROSCI.1859-07.2007}}</ref> The NAcc is associated with acquiring and eliciting conditioned behaviors and involved in the increased sensitivity to drugs as addiction progresses.<ref name="Jones and Bonci"/>
  +
* The [[prefrontal cortex]], more specifically the [[anterior cingulate]] and [[orbitofrontal cortex|orbitofrontal]] cortices,<ref name="Kalivas and Volkow"/> is important for the integration of information which contributes to whether a behavior will be elicited. It appears to be the area in which motivation originates and the salience of stimuli are determined.<ref name="Floresco">{{cite journal |author=Floresco SB, Ghods-Sharifi S |title=Amygdala-prefrontal cortical circuitry regulates effort-based decision making |journal=Cereb. Cortex |volume=17 |issue=2 |pages=251–60 |year=2007 |pmid=16495432 |doi=10.1093/cercor/bhj143}}</ref>
  +
* The [[basolateral amygdala]] projects into the NAcc and is thought to be important for motivation as well.<ref name="Floresco"/>
  +
* More evidence is pointing towards the role of the [[hippocampus]] in drug addiction because of its importance in learning and memory. Much of this evidence stems from investigations manipulating cells in the hippocampus alters dopamine levels in NAcc and firing rates of VTA dopaminergic cells.<ref name="Eisch and Harburg"/>
   
  +
===Stress response===
The mechanisms by which different substances activate the reward system vary among drug classes.
 
  +
In addition to the reward circuit, it is hypothesized that stress mechanisms also play a role in addiction. Koob and Kreek have hypothesized that during drug use [[corticotropin-releasing hormone| corticotropin-releasing factor]] (CRF) activates the [[hypothalamic-pituitary-adrenal axis]] (HPA) and other stress systems in the extended [[amygdala]]. This activation influences the dysregulated emotional state associated with drug addiction. They have found that as drug use escalates, so does the presence of CRF in human [[cerebrospinal fluid]] (CSF). In rat models, the separate use of CRF antagonists and CRF receptor antagonists both decreased self-administration of the drug of study. Other studies in this review showed a dysregulation in other hormones associated with the HPA axis, including [[enkephalin]] which is an endogenous [[opioid peptides]] that regulates pain. It also appears that the [[mu Opioid receptor|µ-opioid receptor]] system, which enkephalin acts on, is influential in the reward system and can regulate the expression of stress hormones.<ref name="Koob and Kreek"/>
   
  +
[[Image:Rational scale to assess the harm of drugs (mean physical harm and mean dependence).svg|thumb|Comparison of the perceived harm for various psychoactive drugs from a poll among medical psychiatrists specialized in addiction treatment<ref name="Nutt">{{cite journal |author=Nutt D, King LA, Saulsbury W, Blakemore C |title=Development of a rational scale to assess the harm of drugs of potential misue |journal=Lancet |volume=369 |issue=9566 |pages=1047–53 |year=2007 |pmid=17382831 |doi=10.1016/S0140-6736(07)60464-4}}</ref>]]
* [[Depressant]]s such as [[alcohol]] and [[benzodiazepine]]s, and [[narcotic]]s such as [[morphine]] and [[methadone]], work by mimicking [[endorphin]]s—chemicals produced naturally by the body which have effects similar to dopamine—or by disabling the [[neuron]]s that normally inhibit the release of dopamine. These substances (sometimes called "downers") typically facilitate relaxation and pain-relief.
 
   
  +
===Behavior===
* [[Stimulant]]s such as [[amphetamine]]s and [[nicotine]] increase dopamine signaling, either by directly stimulating its release, or by blocking its absorption (see "[[reuptake]]"). These substances (sometimes called "uppers") typically cause heightened alertness and energy.
 
  +
Understanding how learning and behavior work in the reward circuit can help understand the action of addictive drugs. Drug addiction is characterized by strong, drug seeking behaviors in which the addict persistently craves and seeks out drugs, despite the knowledge of harmful consequences.<ref name="Kalivas and Volkow"/><ref name="Koob and Kreek"/> Addictive drugs produce a reward, which is the euphoric feeling resulting from sustained DA concentrations in the synaptic cleft of neurons in the brain. [[Operant conditioning]] is exhibited in drug addicts as well as laboratory mice, rats, and primates; they are able to associate an action or behavior, in this case seeking out the drug, with a reward, which is the effect of the drug.<ref name="Jones and Bonci"/> Evidence shows that this behavior is most likely a result of the synaptic changes which have occurred due to repeated drug exposure.<ref name="Kalivas and Volkow"/><ref name="Koob and Kreek"/><ref name="Jones and Bonci"/> The drug seeking behavior is induced by glutamatergic projections from the prefrontal cortex to the NAc. This idea is supported with data from experiments showing the drug seeking behavior can be prevented following the inhibition of [[AMPA]] glutamate receptors and glutamate release in the NAc.<ref name="Kalivas and Volkow"/>
   
  +
===Allostasis===
The most common drug addictions are to legal substances such as:
 
  +
[[Allostasis]] is the process of achieving stability through changes in behavior as well as physiological features. As a person progresses into drug addiction, he or she appears to enter a new allostatic state, defined as divergence from normal levels of change which persist in a chronic state. Addiction to drugs can cause damage to your brain and body as you enter the pathological state; the cost stemming from damage is known as allostatic load. The dysregulation of allostasis gradually occurs as the reward from the drug decreases and the ability to overcome the depressed state following drug use begins to decrease as well. The resulting allostatic load creates a constant state of depression relative to normal allostatic changes. What pushes this decrease is the propensity of drug users to take the drug before the brain and body have returned to original allostatic levels, producing a constant state of stress. Therefore, the presence of environmental stressors may induce stronger drug seeking behaviors.<ref name="Koob and Kreek"/>
* [[Alcohol]]
 
* [[Nicotine]] in the form of [[tobacco]], particularly [[cigarette]]s
 
* [[Caffeine]] in the form of [[tea]], [[coffee]], and caffeinated sodas
 
   
  +
===Neuroplasticity===
Many [[prescription]] or [[over the counter]] drugs can become addictive if abused. [[anabolic steroid|Steroidal]] medications, for example, are extremely addictive. In addition, a large number of other substances are currently considered to have no medical value and are not available over the counter or by prescription. Depending on the jurisdiction, these drugs may be legal only as part of a government sponsored study, illegal to use for any purpose, illegal to sell, or even illegal to merely possess.
 
  +
[[Neuroplasticity]] is the putative mechanism behind learning and memory. It involves physical changes in the synapses between two communicating neurons, characterized by increased gene expression, altered cell signaling, and the formation of new synapses between the communicating neurons. When addictive drugs are present in the system, they appear to hijack this mechanism in the reward system so that motivation is geared towards procuring the drug rather than natural rewards.<ref name="Jones and Bonci"/> Depending on the history of drug use, excitatory synapses in the [[nucleus accumbens]](NAc) experience two types of neuroplasticity: [[long-term potentiation]] (LTP) and [[long-term depression]] (LTD). Using mice as a model, Kourrich ''et al.'' showed that chronic exposure to cocaine increases the strength of synapses in NAc after a 10-14 day withdrawal period, while strengthened synapses did not appear within a 24 hour withdrawal period after repeated cocaine exposure. A single dose of cocaine did not elicit any attributes of a strengthened synapse. When drug-experienced mice were challenged with one dose of cocaine, synaptic depression occurred. Therefore, it seems the history of cocaine exposure along with withdrawal times affects the direction of glutamatergic plasticity in the NAc.<ref name="Kourrich"/>
   
  +
Once a person has transitioned from drug use to addiction, behavior becomes completely geared towards seeking the drug, even though addicts report the euphoria is not as intense as it once was. Despite the differing actions of drugs during acute use, the final pathway of addiction is the same. Another aspect of drug addiction is a decreased response to normal biological stimuli, such as food, sex, and social interaction. Through functional brain imaging of patients addicted to cocaine, scientists have been able to visualize increased metabolic activity in the [[anterior cingulate]] and [[orbitofrontal cortex]] (areas of the prefrontal cortex) in the brain of these subjects. The hyperactivity of these areas of the brain in addicted subjects is involved in the more intense motivation to find the drug rather than seeking natural rewards, as well as an addict’s decreased ability to overcome this urge. Brain imaging has also shown cocaine-addicted subjects to have decreased activity, as compared to non-addicts, in their prefrontal cortex when presented with stimuli associated with natural rewards. The transition from recreational drug use to addiction occurs in gradual stages and is produced by the effect of the drug of choice on the neuroplasticity of the neurons found in the reward circuit. During events preceding addiction, cravings are produced by the release of DA in the prefrontal cortex. As a person transitions from drug use to addiction, the release of dopamine (DA) in the NAc becomes unnecessary to produce cravings; rather, DA transmission decreases while increased metabolic activity in the orbitofrontal cortex contributes to cravings. At this time a person may experience the signs of depression if cocaine is not used. <ref> AJ Giannini. Drug abuse and depression: Catecholamine depletion suggested as biological tie between cocaine withdrawal and depression. National Institute of Drug Abuse Notes. 2(2)5, 1987. </ref> Before a person becomes addicted and exhibits drug-seeking behavior, there is a time period in which the neuroplasticity is reversible. Addiction occurs when drug-seeking behavior is exhibited and the vulnerability to relapse persists, despite prolonged withdrawal; these behavioral attributes are the result of neuroplastic changes which are brought about by repeated exposure to drugs and are relatively permanent.<ref name="Kalivas and Volkow"/>
In [[1972]], [[United States]] President [[Richard Nixon]] declared a [[War on Drugs|war on illegal drugs]] in an attempt to control the growing problem of drug addiction and drug-related [[crime]]. It is unclear, though, whether laws against drugs do anything to stem usage and dependency. In jurisdictions where addictive drugs are illegal, they are generally supplied by [[drug dealer]]s, who are often involved with [[organized crime]]. Even though the cost of producing most illegal addictive substances is very low, their illegality combined with the addict's need permits the seller to command a premium price, often hundreds of times the production cost. As a result, the addict must often turn to crime to support his habit.
 
   
  +
The exact mechanism behind a drug molecule’s effect on synaptic plasticity is still unclear. However, neuroplasticity in glutamatergic projections seems to be a major result of repeated drug exposure. There are several ways in which glutamate transmission is altered. One way is by increasing presynaptic release of glutamate and the other is increased response to glutamate.<ref name="Kalivas and Volkow"/><ref name="Jones and Bonci"/> The two main glutamate receptors involved are [[NMDAR]] and [[AMPAR]]. The expression of these receptors on the cell surface increases with repeated drug use. This type of synaptic plasticity results in LTP, which strengthens connections between two neurons; onset of this occurs quickly and the result is constant. In addition to glutamatergic neurons, dopaminergic neurons present in the VTA respond to glutamate and may be recruited earliest during neural adaptations caused by repeated drug exposure. As shown by Kourrich, et al, history of drug exposure and the time of withdrawal from last exposure appear to play an important role in the direction of plasticity in the neurons of the reward system.<ref name="Jones and Bonci"/>
==Recovery from drug addiction==
 
   
  +
An aspect of neuron development that may also play a part in drug-induced neuroplasticity is the presence of axon guidance molecules such as semaphorins and ephrins. After repeated cocaine treatment, altered expression (increase or decrease dependent on the type of molecule) of mRNA coding for axon guidance molecules occurred in rats. This may contribute to the alterations in the reward circuit characteristic of drug addiction.<ref name="Bahi and Dreyer">{{cite journal |author=Bahi A, Dreyer JL |title=Cocaine-induced expression changes of axon guidance molecules in the adult rat brain |journal=Mol. Cell. Neurosci. |volume=28 |issue=2 |pages=275–91 |year=2005 |pmid=15691709 |doi=10.1016/j.mcn.2004.09.011}}</ref>
Methods of recovery from addiction to drugs vary widely according to the types of drugs involved, amount of drugs used, duration of the drug addiction, medical complications and the social needs of the individual. Treatment is just as important for the addicted individual as for the significant others in the addicted individuals sphere of contact.
 
   
  +
===Neurogenesis===
One of many recovery methods is the [[Twelve-step program|12 Step]] recovery programs. They are commonly known and used for a variety of addictions for the individual addicted and the family of the individual. [[Substance-abuse rehabilitation]] (or "rehab") centers frequently offer a residential treatment program for the seriously addicted in order to isolate the patient from drugs and interactions with other users and dealers. Outpatient clinics usually offer a combination of individual [[counseling]] and group counseling. Frequently a physician or Psychiatrist will assist with [[pharmacology|prescriptions]] to assist with the side effects of the addiction (the most common side effect that the medications can help is anxiety).
 
  +
Drug addiction also raises the issue of potential harmful effects on the development of new neurons in adults. Eisch and Harburg raise three new concepts they have extrapolated from the numerous recent studies on drug addiction. First, [[neurogenesis]] decreases as a result of repeated exposure to addictive drugs. A list of studies show that chronic use of opiates, psychostimulants, nicotine, and alcohol decrease neurogenesis in mice and rats. Second, this apparent decrease in neurogenesis seems to be independent of HPA axis activation. Other environmental factors other than drug exposure such as age, stress and exercise, can also have an effect of neurogenesis by regulating the hypothalamic-pituitary-adrenal (HPA) axis. Mounting evidence suggests this for 3 reasons: small doses of opiates and psychostimulants increase coricosterone concentration in serum but with no effect of neurogenesis; although decreased neurogenesis is similar between self-administered and forced drug intake, activation of HPA axis is greater in self-administration subjects; and even after the inhibition of opiate induced increase of corticosterone, a decrease in neurogenesis occurred. These, of course, need to be investigated further. Last, addictive drugs appear to only affect proliferation in the [[neurogenesis|subgranular zone]] (SGZ), rather than other areas associated with neurogenesis. The studies of drug use and neurogenesis may have implications on stem cell biology.<ref name="Eisch and Harburg"/>
   
  +
===Psychological drug tolerance===
Other forms of treatment involvement replacement drugs such as [[methadone]]. Although methadone is itself addictive, opium dependency is often so strong that the gradual tapering of a less-addictive substance is the only way to reliably treat the user. Other treatments, such as [[acupuncture]], may be used to help alleviate symptoms as well.
 
  +
<!--Psychological drug tolerance redirects here-->
  +
The reward system is partly responsible for the [[psychological]] part of [[drug tolerance]];
   
  +
The [[CREB]] protein, a [[transcription factor]] activated by [[cyclic adenosine monophosphate]] (cAMP) immediately after a high, triggers [[gene]]s that produce proteins such as [[dynorphin]], which cuts off dopamine release and temporarily inhibits the reward circuit. In chronic drug users, a sustained activation of CREB thus forces a larger dose to be taken to reach the same effect. In addition it leaves the user feeling generally depressed and dissatisfied, and unable to find pleasure in previously enjoyable activities, often leading to a return to the drug for an additional "fix".<ref> AJ Giannini. RQ Quinones, DM Martin. Role of beta-endorphin and cAMP in addiction and mania. Society for Neuroscience Abstracts.15:149,1998. </ref>.
Many different ideas circulate regarding what is considered a "successful" outcome in the recovery from addiction. It has widely been established that abstinence from addictive substances is the generally accepted goal.
 
   
  +
===Sensitization===
==Medical definitions==
 
  +
<!--Drug sensitization redirect here-->
  +
Sensitization is the increase in sensitivity to a drug after prolonged use. The proteins [[delta FosB]] and regulator of G-protein Signaling 9-2 (RGS 9-2) are thought to be involved:
   
  +
A transcription factor, known as delta FosB, is thought to activate genes that, counter to the effects of CREB, actually increase the user's sensitivity to the effects of the substance. Delta FosB slowly builds up with each exposure to the drug and remains activated for weeks after the last exposure—long after the effects of CREB have faded. The hypersensitivity that it causes is thought to be responsible for the intense cravings associated with drug addiction, and is often extended to even the peripheral cues of drug use, such as related behaviors or the sight of drug paraphernalia. There is some evidence that delta FosB even causes structural changes within the [[nucleus accumbens]], which presumably helps to perpetuate the cravings, and may be responsible for the high incidence of relapse that occur in treated drug addicts.
The 1957 [[World Health Organization]] (WHO) Expert Committee on Addiction-Producing Drugs defined addiction and habituation as components of [[drug abuse]]:
 
   
  +
Regulator of G-protein Signaling 9-2 (RGS 9-2) has recently been the subject of several animal knockout studies. Animals lacking RGS 9-2 appear to have increased sensitivity to dopamine receptor agonists such as cocaine and amphetamines; over-expression of RGS 9-2 causes a lack of responsiveness to these same agonists. RGS 9-2 is believed to catalyze inactivation of the G-protein coupled D2 receptor by enhancing the rate of GTP hydrolysis of the G alpha subunit which transmits signals into the interior of the cell.
<blockquote>''Drug addiction is a state of periodic or chronic intoxication produced by the repeated consumption of a drug (natural or synthetic). Its characteristics include: (i) an overpowering desire or need (compulsion) to continue taking the drug and to obtain it by any means; (ii) a tendency to increase the dose; (iii) a psychic (psychological) and generally a physical dependence on the effects of the drug; and (iv) detrimental effects on the individual and on society.''</blockquote>
 
   
  +
==Individual mechanisms of effect==
<blockquote>''Drug habituation (habit) is a condition resulting from the repeated consumption of a drug. Its characteristics include (i) a desire (but not a compulsion) to continue taking the drug for the sense of improved well-being which it engenders; (ii) little or no tendency to increase the dose; (iii) some degree of psychic dependence on the effect of the drug, but absence of physical dependence and hence of an abstinence syndrome [withdrawal], and (iv) detrimental effects, if any, primarily on the individual.''</blockquote>
 
  +
The basic mechanisms by which different substances activate the [[reward system]] are as described above, but vary slightly among drug classes.<ref> NS Miller, AJ Giannini. The disease model of addiction. Journal of Psychoactive Drugs.22(1):83-85,1990</ref>.
   
  +
===Depressants===
In 1964, a new WHO committee found these definitions to be inadequate, and suggested using the blanket term 'drug dependence':
 
  +
[[Depressant]]s such as [[alcohol]] and [[benzodiazepine]]s work by increasing the affinity of the GABA receptor for its ligand; GABA. [[Narcotic]]s such as [[morphine]] and [[methadone]], work by mimicking [[endorphin]]s—chemicals produced naturally by the body which have effects similar to dopamine—or by disabling the [[neuron]]s that normally inhibit the release of dopamine in the reward system. These substances (sometimes called "downers") typically facilitate relaxation and pain-relief.
   
  +
===Stimulants===
<blockquote>''The definition of addiction gained some acceptance, but confusion in the use of the terms addiction and habituation and misuse of the former continued. Further, the list of drugs abused increased in number and diversity. These difficulties have become increasingly apparent and various attempts have been made to find a term that could be applied to drug abuse generally. The component in common appears to be dependence, whether psychic or physical or both. Hence, use of the term 'drug dependence', with a modifying phase linking it to a particular drug type in order to differentiate one class of drugs from another, had been given most careful consideration. The Expert Committee recommends substitution of the term 'drug dependence' for the terms 'drug addiction' and 'drug habituation'.''</blockquote>
 
  +
[[Stimulant]]s such as [[amphetamine]]s, [[nicotine]], and [[cocaine]], increase dopamine signaling in the reward system either by directly stimulating its release, or by blocking its absorption (see "[[reuptake]]"). These substances (sometimes called "uppers") typically cause heightened alertness and energy. They cause a pleasant feeling in the body, and euphoria, known as a high. This high wears off leaving the user feeling depressed. This sometimes makes them want more of the drug, and can worsen the addiction.
   
  +
==Theories about causes for epidemic outbreak of addiction==
The committee did not clearly define dependence, but did go on to clarify that there was a distinction between physical and psychological ('psychic') dependence. It said that drug abuse was "''a state of psychic dependence or physical dependence, or both, on a drug, arising in a person following administration of that drug on a periodic or continued basis.''" Psychic dependence was defined as a state in which "''there is a feeling of satisfaction and psychic drive that requires periodic or continuous administration of the drug to produce pleasure or to avoid discomfort''" and all drugs were said to be capable of producing this state:
 
  +
====Nils Bejerot====
  +
[[Nils Bejerot]] (1921 –1988) was a Swedish [[psychiatrist]] and [[criminologist]]. He attacked the symptom theory of addiction - that addictions are a symptom of other more fundamental personal or socioeconomic problems - and separated five essential factors from all of the other factors that are involved in addiction. Bejerot's point was that all of these other factors should be understood as susceptibility or risk factors. Therefore mental illness may make someone susceptible to drug experimentation and use, but it is not a causal factor. Similarly, poverty may increase susceptibility, but there is no automatic causal relationship with addiction. Many poverty-stricken communities are free of addiction [[epidemics]], as are many people with mental illness.
  +
  +
Bejerot's analysis was that the presence of five factors on their own constitutes a risk that an individual will become an addict, or that a community will be affected by an epidemic of addiction:
  +
  +
* Availability of the addictive substance
  +
* Money to acquire the substance
  +
* Time to use the substance
  +
* Example of use of the substance in the immediate environment
  +
* A permissive ideology in relation to the use of the substance. <ref>[http://www.theaustralian.news.com.au/story/0,25197,23299086-5013477,00.html Noel Pearson: Agendas of addiction, 2008]</ref>
  +
  +
Bejerot's opinion was that drug addicts must be prosecuted. This does not mean that Bejerot proposed what he called the harsh American sentences. - The society must (in his view), however, make it very uncomfortable to abuse illicit drugs. <ref>[http://www.rns.se/swedish-addiction.asp Nils Bejerot: Swedish addiction epidemic in an international perspective, 1988]</ref> Drug addict should be offered treatment, mandatory if necessary, but not treatment that helped them to continue the abuse of the drug.
  +
  +
==Treatment==
  +
Treatments for drug addiction vary widely according to the types of drugs involved, amount of drugs used, duration of the drug addiction, medical complications and the social needs of the individual.
  +
  +
Determining the best type of recovery program for an addicted person depends on a number of factors, including: personality, drug(s) of addiction, concept of spirituality or religion, mental or physical illness, and local availability and affordability of programs.
  +
  +
Many different ideas circulate regarding what is considered a "successful" outcome in the recovery from addiction. It has widely been established that abstinence from addictive substances is generally accepted as a "successful" outcome, however differences of opinion exist as to the extent of abstinence required.
  +
  +
In the USA and in many other countries, the goal of treatment for drug dependence is generally total abstinence from all drugs, which while theoretically the ideal outcome, is in practice often very difficult to achieve. Other countries particularly in Europe argue the aims of treatment for drug dependence to be more complex, with treatment aims including reduction in use to the point that drug use no longer interferes with normal activities such as work and family commitments, shifts away from more dangerous routes of drug administration such as injecting to safer routes such as oral administration, reduction in crime committed by drug addicts, and treatment of other comorbid conditions such as AIDS, hepatitis and mental health disorders. These kind of outcomes can often be achieved without necessarily eliminating drug use completely, and so drug treatment programs in Europe often report more favourable outcomes than those in the USA because the criteria for measuring success can be met even though drug users on the programme may still be using drugs to some extent.<ref name="Ball and van de Wijngaart">{{cite journal |author=Ball JC, van de Wijngaart GF |title=A Dutch addict's view of methadone maintenance--an American and a Dutch appraisal |journal=[[Addiction (journal)|Addiction]] |volume=89 |issue=7 |pages=799–802; discussion 803–14 |year=1994 |pmid=8081178 |doi=}}</ref><ref name="Reynolds">{{cite journal |author=Reynolds M, Mezey G, Chapman M, Wheeler M, Drummond C, Baldacchino A |title=Co-morbid post-traumatic stress disorder in a substance misusing clinical population |journal=Drug Alcohol Depend |volume=77 |issue=3 |pages=251–8 |year=2005 |pmid=15734225 |doi=10.1016/j.drugalcdep.2004.08.017}}</ref><ref name="Moggi">{{cite journal |author=Moggi F, Giovanoli A, Strik W, Moos BS, Moos RH |title=Substance use disorder treatment programs in Switzerland and the USA: Program characteristics and 1-year outcomes |journal=Drug Alcohol Depend |volume=86 |issue=1 |pages=75–83 |year=2007 |pmid=16782286 |doi=10.1016/j.drugalcdep.2006.05.017}}</ref>
  +
The supporters of programs with total abstinence from drugs as a goal stress that enabling further drug use mean prolonged drug use and a risk for an increase of total number of addicts; the participants in the program can introduce new users in the habit. <ref>{http://www.rns.se/swedish-addiction.asp Nils Bejerot: The Swedish Addiction Epidemic in global perspective]</ref>
  +
  +
  +
Drug addiction is a complex but treatable brain disease. It is characterized by compulsive drug craving, seeking, and use that persist even in the face of severe adverse consequences. For many people, drug addiction becomes chronic, with relapses possible even after long periods of abstinence. In fact, relapse to drug abuse occurs at rates similar to those for other well-characterized, chronic medical illnesses such as diabetes, hypertension, and asthma. As a chronic, recurring illness, addiction may require repeated treatments to increase the intervals between relapses and diminish their intensity, until abstinence is achieved. Through treatment tailored to individual needs, people with drug addiction can recover and lead productive lives.
  +
The ultimate goal of drug addiction treatment is to enable an individual to achieve lasting abstinence, but the immediate goals are to reduce drug abuse, improve the patient's ability to function, and minimize the medical and social complications of drug abuse and addiction. Like people with diabetes or heart disease, people in treatment for drug addiction will need to change behavior to adopt a more healthful lifestyle.<ref>[http://www.nida.nih.gov/Infofacts/treatmeth.html InfoFacts - Treatment Approaches for Drug Addiction<!-- Bot generated title -->]</ref>
  +
  +
===Residential===
  +
Residential drug treatment can be broadly divided into two camps: 12 step programs or Therapeutic Communities. 12 step programs have the advantage of coming with an instant social support network though some find the spiritual context not to their taste. In the UK drug treatment is generally moving towards a more integrated approach with rehabs offering a variety of approaches. These other programs may use [[Cognitive-Behavioral Therapy]] an approach that looks at the relationship between thoughts feelings and behaviors, recognizing that a change in any of these areas can affect the whole. CBT sees addiction as a behavior rather than a disease and subsequently curable, or rather, unlearnable. CBT programs recognize that for some individuals controlled use is a more realistic possibility.
  +
<ref> AJ Giannini. Alexythymia,affective disorders and substance abuse:possible cross relationships. Psychological Reports.78:1389-1391, 1996.</ref>
  +
  +
====12 step program====
  +
One of many recovery methods is the [[Twelve-step program|12 step]] recovery program, with prominent examples including [[Alcoholics Anonymous]] and [[Narcotics Anonymous]]. They are commonly known and used for a variety of addictions for the individual addicted and the family of the individual. [[Substance-abuse rehabilitation]] (or "rehab") centers frequently offer a residential treatment program for the seriously addicted in order to isolate the patient from drugs and interactions with other users and dealers. Outpatient clinics usually offer a combination of individual [[counseling]] and group counseling. Frequently a physician or psychiatrist will assist with [[pharmacology|prescriptions]] to assist with the side effects of the addiction (the most common side effect that the medications can help is anxiety).
  +
  +
===Anti-addictive drugs===
  +
Other forms of treatment include replacement drugs such as [[methadone]] or [[buprenorphine]], used as a substitute for illicit opiate drugs.<ref>{{cite journal |author=Johnson RE, Chutuape MA, Strain EC, Walsh SL, Stitzer ML, Bigelow GE |title=A comparison of levomethadyl acetate, buprenorphine, and methadone for opioid dependence |journal=N. Engl. J. Med. |volume=343 |issue=18 |pages=1290–7 |year=2000 |pmid=11058673|doi=10.1056/NEJM200011023431802}}</ref><ref>{{cite journal |author=Connock M, Juarez-Garcia A, Jowett S, ''et al'' |title=Methadone and buprenorphine for the management of opioid dependence: a systematic review and economic evaluation |journal=Health Technol Assess |volume=11 |issue=9 |pages=1–171, iii–iv |year=2007 |pmid=17313907 |doi=}}</ref> Although these drugs are themselves addictive, opioid dependency is often so strong that a way to stabilize levels of opioid needed and a way to gradually reduce the levels of opioid needed are required. In some countries, other opioid derivatives such as [[levomethadyl acetate]],<ref>{{cite journal |author=Marsch LA, Stephens MA, Mudric T, Strain EC, Bigelow GE, Johnson RE |title=Predictors of outcome in LAAM, buprenorphine, and methadone treatment for opioid dependence |journal=Exp Clin Psychopharmacol |volume=13 |issue=4 |pages=293–302 |year=2005 |pmid=16366759 |doi=10.1037/1064-1297.13.4.293}}</ref> [[dihydrocodeine]],<ref>{{cite journal |author=Robertson JR, Raab GM, Bruce M, McKenzie JS, Storkey HR, Salter A |title=Addressing the efficacy of dihydrocodeine versus methadone as an alternative maintenance treatment for opiate dependence: A randomized controlled trial |journal=[[Addiction (journal)|Addiction]] |volume=101 |issue=12 |pages=1752–9 |year=2006 |pmid=17156174 |doi=10.1111/j.1360-0443.2006.01603.x}}</ref> [[dihydroetorphine]]<ref>{{cite journal |author=Qin Bo-Yi |title=Advances in dihydroetorphine: From analgesia to detoxification |journal=Drug Development Research|volume=39|issue=2 |pages=131–134 |year=1998|pmid=|doi=}} [http://www3.interscience.wiley.com/cgi-bin/abstract/67067/ABSTRACT?CRETRY=1&SRETRY=0 Link]</ref> and even [[heroin]]<ref name="Metrebian1">{{cite journal |author=Metrebian N, Shanahan W, Wells B, Stimson GV |title=Feasibility of prescribing injectable heroin and methadone to opiate-dependent drug users: associated health gains and harm reductions |journal=Med. J. Aust. |volume=168 |issue=12 |pages=596–600 |year=1998 |pmid=9673620 |doi=}}</ref><ref name="Metrebian2">{{cite journal |author=Metrebian N, Mott J, Carnwath Z, Carnwath T, Stimson GV, Sell L |title=Pathways into receiving a prescription for diamorphine (heroin) for the treatment of opiate dependence in the United kingdom |journal=Eur Addict Res |volume=13 |issue=3 |pages=144–7 |year=2007 |pmid=17570910 |doi=10.1159/000101550}}</ref> are used as substitute drugs for illegal street opiates, with different drugs being used depending on the needs of the individual patient.<ref>{{cite journal |author=Kenna GA, Nielsen DM, Mello P, Schiesl A, Swift RM |title=Pharmacotherapy of dual substance abuse and dependence |journal=CNS Drugs |volume=21 |issue=3 |pages=213–37 |year=2007 |pmid=17338593|doi=10.2165/00023210-200721030-00003}}</ref>
  +
  +
Substitute drugs for other forms of drug dependence have historically been less successful than opioid substitute treatment, but some limited success has been seen with drugs such as [[dexamphetamine]] to treat stimulant addiction,<ref>{{cite journal |author=Mattick RP, Darke S |title=Drug replacement treatments: is amphetamine substitution a horse of a different colour? |journal=Drug Alcohol Rev |volume=14 |issue=4 |pages=389–94 |year=1995 |pmid=16203339 |doi=10.1080/09595239500185531}}</ref><ref>{{cite journal |author=White R |title=Dexamphetamine substitution in the treatment of amphetamine abuse: an initial investigation |journal=[[Addiction (journal)|Addiction]] |volume=95 |issue=2 |pages=229–38 |year=2000 |pmid=10723851 |doi=}}</ref> and [[clomethiazole]] to treat alcohol addiction.<ref>{{cite journal |author=Majumdar SK |title=Chlormethiazole: current status in the treatment of the acute ethanol withdrawal syndrome |journal=Drug Alcohol Depend |volume=27 |issue=3 |pages=201–7 |year=1991 |pmid=1884662|doi=10.1016/0376-8716(91)90001-F}}</ref> [[Bromocriptine]] and [[desipramine]] have been reported to be effective for treatment of cocaine but not amphetamine addiction.<ref> AJ Giannini,TA Billet. Bromocriptine-desipramine protocol in cocaine detoxification. Journal of Clinical Pharmacology. 27:549-554,1987.</ref>
  +
  +
Other pharmacological treatments for alcohol addiction include drugs like [[disulfiram]], [[acamprosate]] and [[topiramate]],<ref>{{cite journal |author=Soyka M, Roesner S |title=New pharmacological approaches for the treatment of alcoholism |journal=Expert Opin Pharmacother |volume=7 |issue=17 |pages=2341–53 |year=2006 |pmid=17109610 |doi=10.1517/14656566.7.17.2341}}</ref><ref>{{cite journal |author=Pettinati HM, Rabinowitz AR |title=Choosing the right medication for the treatment of alcoholism |journal=Curr Psychiatry Rep |volume=8 |issue=5 |pages=383–8 |year=2006 |pmid=16968619|doi=10.1007/s11920-006-0040-0}}</ref> but rather than substituting for alcohol, these drugs are intended to reduce the desire to drink, either by directly reducing cravings as with acamprosate and topiramate, or by producing unpleasant effects when alcohol is consumed, as with disulfiram. These drugs can be effective if treatment is maintained, but compliance can be an issue as alcoholic patients often forget to take their medication, or discontinue use because of excessive side effects.<ref>{{cite journal |author=Bouza C, Angeles M, Magro A, Muñoz A, Amate JM |title=Efficacy and safety of naltrexone and acamprosate in the treatment of alcohol dependence: a systematic review |journal=[[Addiction (journal)|Addiction]] |volume=99 |issue=7 |pages=811–28 |year=2004 |pmid=15200577 |doi=10.1111/j.1360-0443.2004.00763.x}}</ref><ref>{{cite journal |author=Williams SH |title=Medications for treating alcohol dependence |journal=Am Fam Physician |volume=72 |issue=9 |pages=1775–80 |year=2005 |pmid=16300039 |doi=}}</ref> Additional drugs acting on [[glutamate]] neurotransmission such as [[modafinil]], [[lamotrigine]], [[gabapentin]] and [[memantine]] have also been proposed for use in treating addiction to alcohol and other drugs.<ref>{{cite journal |author=Gass JT, Olive MF |title=Glutamatergic substrates of drug addiction and alcoholism |journal=Biochem. Pharmacol. |volume=75 |issue=1 |pages=218–65 |year=2008 |pmid=17706608 |doi=10.1016/j.bcp.2007.06.039}}</ref>
  +
  +
Opioid antagonists such as [[naltrexone]] and [[nalmefene]] have also been used successfully in the treatment of alcohol addiction,<ref>{{cite journal |author=Srisurapanont M, Jarusuraisin N |title=Opioid antagonists for alcohol dependence |journal=Cochrane Database Syst Rev |volume= |issue=1 |pages=CD001867 |year=2005 |pmid=15674887 |doi=10.1002/14651858.CD001867.pub2}}</ref><ref>{{cite journal |author=Karhuvaara S, Simojoki K, Virta A, ''et al'' |title=Targeted nalmefene with simple medical management in the treatment of heavy drinkers: a randomized double-blind placebo-controlled multicenter study |journal=Alcohol. Clin. Exp. Res. |volume=31 |issue=7 |pages=1179–87 |year=2007 |pmid=17451401 |doi=10.1111/j.1530-0277.2007.00401.x}}</ref> which is often particularly challenging to treat. These drugs have also been used to a lesser extent for long-term maintenance treatment of former opiate addicts, but cannot be started until the patient has been abstinent for an extended period, otherwise they can trigger acute opioid withdrawal symptoms.<ref>{{cite journal |author=Comer SD, Sullivan MA, Hulse GK |title=Sustained-release naltrexone: novel treatment for opioid dependence |journal=Expert Opin Investig Drugs |volume=16 |issue=8 |pages=1285–94 |year=2007 |pmid=17685876 |doi=10.1517/13543784.16.8.1285}}</ref>
  +
  +
Treatment of [[stimulant]] addiction can often be difficult, with substitute drugs often being ineffective, although newer drugs such as [[nocaine]], [[vanoxerine]] and [[modafinil]] may have more promise in this area, as well as the GABA<sub>B</sub> agonist [[baclofen]].<ref>{{cite journal |author=Ling W, Rawson R, Shoptaw S, Ling W |title=Management of methamphetamine abuse and dependence |journal=Curr Psychiatry Rep |volume=8 |issue=5 |pages=345–54 |year=2006 |pmid=16968614|doi=10.1007/s11920-006-0035-x}}</ref><ref>{{cite journal |author=Preti A |title=New developments in the pharmacotherapy of cocaine abuse |journal=Addict Biol |volume=12 |issue=2 |pages=133–51 |year=2007 |pmid=17508985 |doi=10.1111/j.1369-1600.2007.00061.x}}</ref> Another strategy that has recently been successfully trialled used a combination of the [[benzodiazepine]] antagonist [[flumazenil]] with [[hydroxyzine]] and [[gabapentin]] for the treatment of [[methamphetamine]] addiction.<ref>{{cite journal |author=Urschel HC, Hanselka LL, Gromov I, White L, Baron M |title=Open-label study of a proprietary treatment program targeting type A gamma-aminobutyric acid receptor dysregulation in methamphetamine dependence |journal=Mayo Clin. Proc. |volume=82 |issue=10 |pages=1170–8 |year=2007 |pmid=17908523 |doi=}}</ref>
  +
  +
Another area in which drug treatment has been widely used is in the treatment of [[nicotine]] addiction. Various drugs have been used for this purpose such as [[bupropion]], [[mecamylamine]] and the more recently developed [[varenicline]]. The cannaboinoid antagonist [[rimonabant]] has also been trialled for treatment of nicotine addiction but has not been widely adopted for this purpose.<ref>{{cite journal |author=Garwood CL, Potts LA |title=Emerging pharmacotherapies for smoking cessation |journal=Am J Health Syst Pharm |volume=64 |issue=16 |pages=1693–8 |year=2007 |pmid=17687057 |doi=10.2146/ajhp060427}}</ref><ref>{{cite journal |author=Frishman WH |title=Smoking cessation pharmacotherapy--nicotine and non-nicotine preparations |journal=Prev Cardiol |volume=10 |issue=2 Suppl 1 |pages=10–22 |year=2007 |pmid=17396063|doi=10.1111/j.1520-037X.2007.05963.x}}</ref><ref>{{cite journal |author=Siu EC, Tyndale RF |title=Non-nicotinic therapies for smoking cessation |journal=Annu. Rev. Pharmacol. Toxicol. |volume=47 |issue= |pages=541–64 |year=2007 |pmid=17209799 |doi=10.1146/annurev.pharmtox.47.120505.105354}}</ref>
  +
  +
[[Ibogaine]] is a psychoactive drug that specifically interrupts the addictive response, and is currently being studied for its effects upon cocaine, heroin, nicotine, and SSRI addicts. Alternative medicine clinics offering ibogaine treatment have appeared along the U.S. border.<ref>{{cite journal |author=Alper KR, Lotsof HS, Kaplan CD |title=The ibogaine medical subculture |journal=J Ethnopharmacol |volume=115 |issue=1 |pages=9–24 |year=2008 |pmid=18029124 |doi=10.1016/j.jep.2007.08.034}}</ref> Ibogaine treatment for drug addiction can be reasonably effective, but potentially dangerous side effects which have been linked to several deaths have limited its adoption by conventional medical practice.<ref>{{cite journal |author=Mash DC, Kovera CA, Pablo J, ''et al'' |title=Ibogaine: complex pharmacokinetics, concerns for safety, and preliminary efficacy measures |journal=Ann. N. Y. Acad. Sci. |volume=914 |issue= |pages=394–401 |year=2000 |pmid=11085338 |doi=}}</ref> A synthetic analogue of ibogaine, [[18-methoxycoronaridine]] has also been developed which has similar efficacy but less side effects, however this drug is still being tested in animals and human trials have not yet been carried out.<ref>{{cite journal |author=Levi MS, Borne RF |title=A review of chemical agents in the pharmacotherapy of addiction |journal=Curr. Med. Chem. |volume=9 |issue=20 |pages=1807–18 |year=2002 |pmid=12369879 |doi=}}</ref><ref>{{cite journal |author=Werneke U, Turner T, Priebe S |title=Complementary medicines in psychiatry: review of effectiveness and safety |journal=Br J Psychiatry |volume=188 |issue= |pages=109–21 |year=2006 |pmid=16449696 |doi=10.1192/bjp.188.2.109}}</ref>
  +
  +
=== Alternative therapies ===
  +
Alternative therapies, such as [[acupuncture]], are used by some practitioners to alleviate the symptoms of drug addiction. In 1997, the American Medical Association (AMA) adopted as policy the following statement after a report on a number of alternative therapies including acupuncture:
  +
<blockquote>There is little evidence to confirm the safety or efficacy of most alternative therapies. Much of the information currently known about these therapies makes it clear that many have not been shown to be efficacious. Well-designed, stringently controlled research should be done to evaluate the efficacy of alternative therapies.</blockquote><!-- source? -->
  +
  +
Acupuncture has been shown to be no more effective than control treatments in the treatment of opiate dependence.<ref>{{cite journal |author=Jordan JB |title=Acupuncture treatment for opiate addiction: a systematic review |journal=J Subst Abuse Treat |volume=30 |issue=4 |pages=309–14 |year=2006 |pmid=16716845 |doi=10.1016/j.jsat.2006.02.005}}</ref> Acupuncture, [[acupressure]], [[laser therapy]] and [[electrostimulation]] have no demonstrated efficacy for smoking cessation.<ref>{{cite journal |author=White AR, Rampes H, Campbell JL |title=Acupuncture and related interventions for smoking cessation |journal=Cochrane Database Syst Rev |volume= |issue=1 |pages=CD000009 |year=2006 |pmid=16437420 |doi=10.1002/14651858.CD000009.pub2}}</ref>
  +
  +
== Medical definitions ==
  +
The terms ''abuse'' and ''addiction'' have been defined and re-defined over the years. The 1957 [[World Health Organization]] (WHO) Expert Committee on Addiction-Producing Drugs defined addiction and habituation as components of [[drug abuse]]:
  +
  +
<blockquote>'''''Drug addiction''' is a state of periodic or chronic intoxication produced by the repeated consumption of a drug (natural or synthetic). Its characteristics include: (i) an overpowering desire or need (compulsion) to continue taking the drug and to obtain it by any means; (ii) a tendency to increase the dose; (iii) a psychic (psychological) and generally a [[physical dependence]] on the effects of the drug; and (iv) detrimental effects on the individual and on society.''</blockquote>
  +
  +
<blockquote>''[[Drug habituation]] (habit) is a condition resulting from the repeated consumption of a drug. Its characteristics include (i) a desire (but not a compulsion) to continue taking the drug for the sense of improved well-being which it engenders; (ii) little or no tendency to increase the dose; (iii) some degree of psychic dependence on the effect of the drug, but absence of physical dependence and hence of an abstinence syndrome [withdrawal], and (iv) detrimental effects, if any, primarily on the individual.''</blockquote>
  +
  +
In 1964, a new WHO committee found these definitions to be inadequate, and suggested using the blanket term "drug dependence":
  +
  +
<blockquote>''The definition of addiction gained some acceptance, but confusion in the use of the terms addiction and habituation and misuse of the former continued. Further, the list of drugs abused increased in number and diversity. These difficulties have become increasingly apparent and various attempts have been made to find a term that could be applied to drug abuse generally. The component in common appears to be dependence, whether psychic or physical or both. Hence, use of the term 'drug dependence', with a modifying phase linking it to a particular drug type in order to differentiate one class of drugs from another, had been given most careful consideration. The Expert Committee recommends substitution of the term 'drug dependence' for the terms 'drug addiction' and 'drug habituation'.''</blockquote>
  +
  +
The committee did not clearly define dependence, but did go on to clarify that there was a distinction between physical and psychological ("psychic") dependence. It said that drug abuse was "''a state of psychic dependence or physical dependence, or both, on a drug, arising in a person following administration of that drug on a periodic or continued basis.''" Psychic dependence was defined as a state in which "''there is a feeling of satisfaction and psychic drive that requires periodic or continuous administration of the drug to produce pleasure or to avoid discomfort''" and all drugs were said to be capable of producing this state:
   
 
<blockquote>''There is scarcely any agent which can be taken into the body to which some individuals will not get a reaction satisfactory or pleasurable to them, persuading them to continue its use even to the point of abuse&nbsp;&mdash; that is, to excessive or persistent use beyond medical need.''</blockquote>
 
<blockquote>''There is scarcely any agent which can be taken into the body to which some individuals will not get a reaction satisfactory or pleasurable to them, persuading them to continue its use even to the point of abuse&nbsp;&mdash; that is, to excessive or persistent use beyond medical need.''</blockquote>
   
The 1957 and 1964 definitions of addiction, dependence and abuse persist to the present day in medical literature. It should be noted that at this time (2006) the Diagnostic Statistical Manual (DSM IVR) now spells out specific criteria for defining abuse and dependence.
+
The 1957 and 1964 definitions of addiction, dependence and abuse persist to the present day in medical literature. It should be noted that at this time (2006) the Diagnostic Statistical Manual (DSM IVR) now spells out specific criteria for defining abuse and dependence. (DSM IVR) uses the term substance dependence instead of ''addiction''; a maladaptive pattern of substance abuse, leading to clinically significant impairment or distress, as manifested by three (or more) specified criteria, occurring at any time in the same 12-month period. This definition is also applicable on drugs with smaller or nonexistent physical signs of withdrawal, for ex. cannabis.
   
In 2001, the American Academy of Pain Medicine, the American Pain Society, and the American Society of Addiction Medicine jointly issued "Definitions Related to the Use of Opioids for the Treatment of Pain," which defined the following terms:
+
In 2001, the American Academy of Pain Medicine, the American Pain Society, and the American Society of Addiction Medicine jointly issued "Definitions Related to the Use of Opioids for the Treatment of Pain," which defined the following terms:<ref name=painmed/>
   
<blockquote>''Addiction is a primary, chronic, neurobiologic disease, with genetic, psychosocial, and environmental factors influencing its development and manifestations. It is characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving.''</blockquote>
+
<blockquote>'''''Addiction''' is a primary, chronic, neurobiologic disease, with genetic, psychosocial, and environmental factors influencing its development and manifestations. It is characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving.
   
<blockquote>''Physical dependence is a state of adaptation that is manifested by a drug class specific withdrawal syndrome that can be produced by abrupt cessation, rapid dose reduction, decreasing blood level of the drug, and/or administration of an antagonist.''</blockquote>
+
<blockquote>''[[Physical dependence]] is a state of adaptation that is manifested by a drug class specific withdrawal syndrome that can be produced by abrupt cessation, rapid dose reduction, decreasing blood level of the drug, and/or administration of an antagonist.''</blockquote>
   
<blockquote>''Tolerance is a state of adaptation in which exposure to a drug induces changes that result in a diminution of one or more of the drug’s effects over time.''</blockquote>
+
<blockquote>''[[drug tolerance|Tolerance]] is the body's physical adaptation to a drug: greater amounts of the drug are required over time to achieve the initial effect as the body "gets used to" and adapts to the intake. </blockquote>
   
<blockquote>''Pseudoaddiction is a term which has been used to describe patient behaviors that may occur when pain is undertreated. Patients with unrelieved pain may become focused on obtaining medications, may “clock watch,” and may otherwise seem inappropriately “drug seeking.” Even such behaviors as illicit drug use and deception can occur in the patient's efforts to obtain relief. Pseudoaddiction can be distinguished from true addiction in that the behaviors resolve when pain is effectively treated''</blockquote>
+
<blockquote>'''''Pseudo addiction''' is a term which has been used to describe patient behaviors that may occur when pain is undertreated. Patients with unrelieved pain may become focused on obtaining medications, may “clock watch,” and may otherwise seem inappropriately “drug seeking.” Even such behaviors as illicit drug use and deception can occur in the patient's efforts to obtain relief. Pseudoaddiction can be distinguished from true addiction in that the behaviors resolve when pain is effectively treated.''</blockquote></blockquote>
   
  +
The [[Diagnostic and Statistical Manual of Mental Disorders]], '''DSM-IV-TR''' doesn’t use the word '''addiction''' at all. Instead it has a section about [[Substance dependence]]
== Drugs considered to be addictive (Some may be debatable) ==
 
  +
<blockquote>''"When an individual persists in use of alcohol or other drugs despite problems related to use of the substance, [[substance dependence]] may be diagnosed. Compulsive and repetitive use may result in tolerance to the effect of the drug and withdrawal symptoms when use is reduced or stopped. This, along with [[Substance Abuse]] are considered Substance Use Disorders...."'' <ref name="DSM4">[http://www.behavenet.com/capsules/disorders/subdep.htm DSM-IV & DSM-IV-TR:Substance Dependence]</ref></blockquote>
   
  +
A definition of '''addiction''' proposed by professor [[Nils Bejerot]]:
* [[Alcohol]]
 
  +
<blockquote>''"An emotional fixation (sentiment) acquired through learning, which intermittently or continually expresses itself in purposeful, stereotyped behavior with the character and force of a natural drive, aiming at a specific pleasure or the avoidance of a specific discomfort."''<ref name="NIDA">[http://www.nida.nih.gov/pdf/monographs/30.pdf Nils Bejerot in Theories of Drug abuse, Selected contemporary perspectives, page 246-255, [[National Institute on Drug Abuse| NIDA]], 1980]</ref>''</blockquote>
* [[Analgesic]]s
 
* [[Barbiturate]]s
 
* [[Buprenorphine]]
 
* [[Butorphanol]]
 
* [[Cannabis]]
 
* [[Chloral hydrate]], [[trichloroethanol]] and derivatives
 
* [[Cocaine]]
 
* [[Codeine]]
 
* [[Dextroproxyp]]
 
* [[Dextromethorphan]]
 
* [[Ethchlorvynol]]
 
* [[Fentanyl]] and its analogs
 
* [[Gamma-hydroxybutyrate]] (GHB)
 
* [[Glutethimide]]
 
* [[Heroin]] (Diacetylmorphine)
 
* [[Hydrocodone]]
 
* [[Hydromorphone]] (Dilaudid®)
 
* [[Ketamine]]
 
* [[Laxative]]s
 
* [[Levo-alpha-acetylmethadol]] (LAAM)
 
* [[Meperidine]]
 
* [[Meprobamate]]
 
* [[Methamphetamine]] and other [[Amphetamine]]s
 
* [[Methaqualone]] and related sedative-hypnotics
 
* [[Methadone]]
 
* [[Methcathinone]]
 
* [[Morphine]]
 
* [[Nicotine]]
 
* [[Oxycodone]]
 
* [[Opium]]
 
* Synthetic [[opioid]] agonists and partial agonists not considered here
 
* Semi-synthetic [[opiates]] not considered here
 
* [[Alprazolam|Xanax]]
 
* [[Paraldehyde]] (Paral®)
 
* [[Phencyclidine]] (PCP)
 
* [[Flunitrazepam]] (Rohypnol®)
 
   
 
== Addiction and drug control legislation ==
 
== Addiction and drug control legislation ==
  +
Depending on the jurisdiction, addictive drugs may be legal only as part of a government sponsored study, illegal to use for any purpose, illegal to sell, or even illegal to merely possess.
   
Most countries have legislation which brings various drugs and drug-like [[substance]]s under the control of licensing systems. Typically this legislation covers any or all of the opiates, canaboids, cocaine, barbiturates, hallucinogenics and a variety of more modern synthetic drugs, and unlicensed production, supply or possession is a criminal offence.
+
Most countries have legislation which brings various drugs and drug-like [[Chemical substance|substances]] under the control of licensing systems. Typically this legislation covers any or all of the opiates, amphetamines, cannabinoids, cocaine, barbiturates, hallucinogenics and a variety of more modern synthetic drugs, and unlicensed production, supply or possession is a criminal offence.
   
Usually, however, drug clasification under such legislation is not related simply to addictiveness. The substances covered often have very different addictive properties. Some are highly prone to cause physical dependency, whilst others rarely cause any form of compulsive need whatsoever. Also, under legislation specifically about drugs, [[alcohol]] is not usually included.
+
Usually, however, drug classification under such legislation is not related simply to addictiveness. The substances covered often have very different addictive properties. Some are highly prone to cause physical dependency, whilst others rarely cause any form of compulsive need whatsoever. Also, under legislation specifically about drugs, [[alcohol]] is not usually included.
   
Although the legislation may be justifiable on moral or public health grounds, it can make addiction or dependency a much more serious issue for the individual: reliable supplies of a drug become difficult to secure, and the individual becomes vulnerable to both criminal abuse and legal punishment.
+
Although the legislation may be justifiable on moral or public health grounds, it can make addiction or dependency a much more serious issue for the individual: reliable supplies of a drug become difficult to secure, and the individual becomes vulnerable to both criminal abuse and legal punishment.
  +
  +
It is unclear whether laws against drugs do anything to stem usage and dependency. In jurisdictions where addictive drugs are illegal, they are generally supplied by [[drug dealer]]s, who are often involved with [[organized crime]]. Even though the cost of producing most illegal addictive substances is very low, their illegality combined with the addict's need permits the seller to command a premium price, often hundreds of times the production cost. As a result, the addict sometimes turns to crime to support their habit.
  +
  +
==History of addiction==
  +
{{Refimprove|section|date=September 2007}}
  +
The [[phenomenon]] of drug [[addiction]] has occurred to some degree throughout recorded [[history]] (see "[[opium]]"). Modern [[agriculture|agricultural]] practices, improvements in access to drugs, advancements in [[biochemistry]], and dramatic increases in the recommendation of drug usage by clinical practitioners have exacerbated the problem significantly in the 20th century. Improved means of active biological agent manufacture and the introduction of synthetic compounds, such as [[methamphetamine]] are also factors contributing to drug addiction.<ref> DCA Hillman. The Chemical Muse. New York City,St. Martin's Press,2008</ref>
   
 
==See also==
 
==See also==
  +
{{col-begin}}
*[[List of heroin addicts]]
 
  +
{{col-2}}
*[[Drug Mix]]
 
  +
*[[Addiction]]
  +
*[[Addiction recovery groups]]
 
*[[Alcoholism]]
 
*[[Alcoholism]]
  +
*[[Arguments for and against drug prohibition]]
  +
*[[Cocaine dependence]]
  +
*[[Demand reduction]]
 
*[[Drug abuse]]
 
*[[Drug abuse]]
  +
*[[Drug abuse liability]]
  +
*[[Drug overdoses]]
  +
*[[Drug policy]]
  +
*[[Drugs and prostitution]]
  +
*[[Poly drug use]]
  +
*[[Drug tolerance]]
  +
*[[Drug Intervention Program]]
  +
*[[Drug withdrawal]]
  +
{{col-2}}
  +
*[[DSM-IV Codes]]
  +
*[[Heroin addiction]]
  +
*[[Harm reduction]]
  +
*[[Intravenous drug use]]
  +
*[[Methadone maintenance]]
  +
*[[Nils Bejerot]]
  +
*[[Physical dependence]]
  +
*[[Polydrug abuse]]
  +
*[[Psychoactive drug]]
  +
*[[Tachyphylaxis]]
  +
*[[Treatment Improvement Protocols]]
 
*[[Rat Park]]
 
*[[Rat Park]]
  +
*[[Rational addiction]]
*''[[Robinson v. California]]'' ([[1964]]), decision by the [[U.S. Supreme Court]] that states cannot criminalize narcotics addiction itself
 
*[[Harm reduction]]
+
*[[Substance dependence]]
*[[Demand reduction]]
+
*[[Self-medication]]
  +
{{col-end}}
*[[Arguments for and against drug prohibition]]
 
 
==External links==
 
* [http://www.usdoj.gov/dea/concern/concern.htm DEA list of drugs and drug types]
 
* [http://www.streetdrugs.org/ www.streetdrugs.org - a reference for what's out there now]
 
* [http://www.ericdigests.org/2003-3/abuse.htm Substance Abuse Prevention and Intervention for Students with Disabilities]
 
* [http://www.ericdigests.org/pre-9221/indian.htm Fighting Alcohol and Substance Abuse among American Indian and Alaskan Native Youth]
 
* [http://www.zerohops.com/drug-test-lettertopresident.html Drug and Detox Research Center Letter to the President]
 
* [http://www.ericdigests.org/pre-922/abuse.htm Adolescent Substance Abuse: Counseling Issues]
 
* [http://www.recoveryhelper.org/ Drug Addiction Recovery Helper]
 
* [http://www.ericdigests.org/2000-3/abuse.htm Substance Abuse and Counseling]
 
* [http://www.ericdigests.org/1993/abuse.htm Substance Abuse Policy]
 
* [http://www.ericdigests.org/pre-9210/drug.htm Stopping Drug Abuse]
 
* [http://rehab.netfirms.com/ Drug Abuse Recovery Guide]
 
* [http://www.newfreedomprograms.com Change Companies Substance Abuse Treatment Programs] (commercial)
 
* [http://www.newfreedomprograms.com New Freedom Programs Substance Abuse and Behavioral Health Treatment] (commercial)
 
* [http://www.whale.to/v/kalokerinos2.html THE ORTHOMOLECULAR TREATMENT OF DRUG ADDICTION by Archie Kalokerinos MD.]
 
   
 
==Literature==
 
==Literature==
* Sainsbury, ''Drugs and the Drug Habit'' (New York, 1909)
+
* Sainsbury, ''Drug and the Drug Habit'' (New York, 1909)
 
* C. A. McBride, ''Modern Treatment of Alcoholism and Drug Narcotism'' (New York, 1910)
 
* C. A. McBride, ''Modern Treatment of Alcoholism and Drug Narcotism'' (New York, 1910)
 
* G. E. Pettey, ''Narcotic Drug Diseases and Allied Ailments'' (Philadelphia, 1913)
 
* G. E. Pettey, ''Narcotic Drug Diseases and Allied Ailments'' (Philadelphia, 1913)
* [[Fitz Hugh Ludlow]] wrote ''The Hasheesh Eater'' (1857) and ''The Opium Habit'' (1868), designed as a warning.
+
* [[Fitz Hugh Ludlow]] wrote ''The Hasheesh Eater'' (1857) and ''The Opium Habit'' (1868), designed as a warning.
  +
* [[Thomas de Quincey]], ''Confessions of an English Opium Eater'' (London, 1822)
  +
* [[William S. Burroughs]], ''Junkie'' (New York, 1953)
  +
 
==References==
 
==References==
  +
{{reflist|2}}
* Nestler, Eric and Malenka, Robert (Mar. 2004). "The Addicted Brain". <i>Scientific American</i>, pg. 78-83.
 
* Leavitt, Fred (2003) The REAL Drug Abusers. Rowman & Littlefield.
 
   
  +
==Sources==
[[Category:Addiction]]
 
  +
* [http://www.dukeupress.edu/books.php3?isbn=978-0-8223-3881-9 ''The Cult of Pharmacology: How America Became the Most Troubled Drug Culture''] by Richard DeGrandpre, Duke University Press, 2006.
[[Category:Drugs]]
 
  +
* Nestler, Eric and Malenka, Robert (March 2004). "The Addicted Brain". ''Scientific American'', pg. 78-83.
  +
* Leavitt, Fred. The REAL Drug Abusers. Rowman & Littlefield, 2003.
  +
  +
==External links==
  +
{{dmoz|Health/Addictions/Substance_Abuse/}}
  +
  +
[[Category:Side effects (drug)
 
[[Category:Substance-related disorders]]
 
[[Category:Substance-related disorders]]
[[Category:Social stigma]]
 
   
  +
[[es:Drogadicción]]
 
  +
  +
<!--
  +
[[bn:মাদকাসক্তি]]
  +
[[bg:Пристрастяване]]
  +
[[ca:Addicció]]
  +
[[cs:Závislost]]
  +
[[da:Narkoman]]
  +
[[de:Missbrauch und Abhängigkeit]]
  +
[[et:Sõltuvus (narkoloogia)]]
  +
[[es:Drogodependencia]]
  +
[[eo:Droga dependeco]]
  +
[[fa:اعتیاد]]
 
[[fr:Toxicomanie]]
 
[[fr:Toxicomanie]]
  +
[[gl:Adicción]]
  +
[[ka:ნარკომანია]]
  +
[[ko:중독]]
  +
[[hy:Թմրամոլություն]]
  +
[[hr:Ovisnost]]
  +
[[id:Kecanduan]]
  +
[[is:Fíkn]]
 
[[it:Tossicodipendenza]]
 
[[it:Tossicodipendenza]]
  +
[[he:התמכרות]]
  +
[[lt:Narkomanija]]
  +
[[hu:Függőség]]
  +
[[nl:Verslaving]]
  +
[[ja:薬物依存症]]
  +
[[no:Narkomani]]
  +
[[oc:Adiccion]]
 
[[pl:Narkomania]]
 
[[pl:Narkomania]]
  +
[[pt:Toxicomania]]
[[ru:&#1085;&#1072;&#1088;&#1082;&#1086;&#1084;&#1072;&#1085;&#1080;&#1103;]]
 
  +
[[ro:Dependenţă]]
  +
[[ru:Наркомания]]
  +
[[scn:Divotu (idiali)]]
  +
[[simple:Drug addiction]]
  +
[[sr:Наркоманија]]
  +
[[sh:Ovisnost]]
  +
[[fi:Päihderiippuvuus]]
  +
[[sv:Narkomani]]
  +
[[tr:Bağımlılık]]
  +
[[uk:Наркоманія]]
  +
[[zh:藥物成癮]]
  +
-->
 
{{enWP|Drug addiction}}
 
{{enWP|Drug addiction}}
  +
[[Category:Alcohol abuse]]
  +
[[Category:Drug addiction| ]]
  +
[[Category:Drug dependency]]
  +
[[Category:Mental health]]

Revision as of 07:28, 1 April 2010

Assessment | Biopsychology | Comparative | Cognitive | Developmental | Language | Individual differences | Personality | Philosophy | Social |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |

Clinical: Approaches · Group therapy · Techniques · Types of problem · Areas of specialism · Taxonomies · Therapeutic issues · Modes of delivery · Model translation project · Personal experiences ·


This article is in need of attention from a psychologist/academic expert on the subject.
Please help recruit one, or improve this page yourself if you are qualified.
This banner appears on articles that are weak and whose contents should be approached with academic caution.
Drug dependence
ICD-10 F1x.2
ICD-9 304
OMIM {{{OMIM}}}
DiseasesDB {{{DiseasesDB}}}
MedlinePlus {{{MedlinePlus}}}
eMedicine {{{eMedicineSubj}}}/{{{eMedicineTopic}}}
MeSH {{{MeshNumber}}}

The World Health Organization defines as

"A state, psychic and sometimes also physical, resulting in the interaction between a living organism and a drug, characterized by behavioral and other responses that always include a compulsion to induce the drug on a continuous or periodic basis so that they may experience its psychic effects, and sometimes to avoid the discomfort of its absences."


Drug addiction is widely considered a pathological state. The disorder of addiction involves the progression of acute drug use to the development of drug-seeking behavior, the vulnerability to relapse, and the decreased, slowed ability to respond to naturally rewarding stimuli. The Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) has categorized three stages of addiction: preoccupation/anticipation, binge/intoxication, and withdrawal/negative affect. These stages are characterized, respectively, everywhere by constant cravings and preoccupation with obtaining the substance; using more of the substance than necessary to experience the intoxicating effects; and experiencing tolerance, withdrawal symptoms, and decreased motivation for normal life activities.[1] By the American Society of Addiction Medicine definition, drug addiction differs from drug dependence and drug tolerance.[2]

It is, both among scientists and other writers, quite usual to allow the concept of drug addiction to include persons who are not drug abusers according to the definition of the American Society of Addiction Medicine. The term drug addiction is then used as a category which may include the same persons who under the DSM-IV can be given the diagnosis of substance dependence or substance abuse. (See also DSM-IV Codes)

Drugs
Brain animated color nevit

Drug type
Drug usage
Drug abuse
Drug treatment

Drugs causing addiction

Drugs known to cause addiction include illegal drugs as well as prescription or over-the-counter drugs, according to the definition of the American Society of Addiction Medicine.


Addictive drugs also include a large number of substrates that are currently considered to have no medical value and are not available over the counter or by prescription.

An article in The Lancet compared the harm and addiction of 20 drugs, using a scale from 0 to 3 for physical addiction, psychological addiction, and pleasure to create a mean score for addiction. Caffeine was not included in the study. The results can be seen in the chart above.

Addictive potency

The addictive potency of drugs varies from substance to substance, and from individual to individual

Drugs such as codeine or alcohol, for instance, typically require many more exposures to addict their users than drugs such as heroin or cocaine. Likewise, a person who is psychologically or genetically predisposed to addiction is much more likely to suffer from it.

Although dependency on hallucinogens like LSD ("acid") and psilocybin (key hallucinogen in "magic mushrooms") is listed as Substance-Related Disorder in the DSM-IV, most psychologists do not classify them as addictive drugs.

Prevalence

The most common drug addictions are to legal substances such as:

The physiological basis of drug addiction

Researchers have conducted numerous investigations using animal models and functional brain imaging on humans in order to define the mechanisms underlying drug addiction in the brain. This intriguing topic incorporates several areas of the brain and synaptic changes, or neuroplasticity, which occurs in these areas.

Acute effects

Acute (or recreational) drug use causes the release and prolonged action of dopamine and serotonin within the reward circuit. Different types of drugs produce these effects by different methods. Dopamine (DA) appears to harbor the largest effect and its action is characterized. DA binds to the D1 receptor, triggering a signaling cascade within the cell. cAMP-dependent protein kinase (PKA) phosphorylates cAMP response element binding protein (CREB), a transcription factor, which induces the synthesis of certain genes including C-Fos.[3]

Reward circuit

When examining the biological basis of drug addition, one must first understand the pathways in which drugs act and how drugs can alter those pathways. The reward circuit, also referred to as the mesolimbic system, is characterized by the interaction of several areas of the brain.

  • The ventral tegmental area (VTA) consists of dopaminergic neurons which respond to glutamate. These cells respond when stimuli indicative of a reward are present. The VTA supports learning and sensitization development and releases dopamine (DA) into the forebrain.[4] These neurons also project and release DA into the nucleus accubems[5], through the mesolimbic pathway. Virtually all drugs causing drug addiction increase the dopamine release in the mesolimbic pathway,[6] in addition to their specific effects.
  • The nucleus accumbens (NAcc) consists mainly of medium-spiny projection neurons (MSNs), which are GABA neurons.[7] The NAcc is associated with acquiring and eliciting conditioned behaviors and involved in the increased sensitivity to drugs as addiction progresses.[4]
  • The prefrontal cortex, more specifically the anterior cingulate and orbitofrontal cortices,[3] is important for the integration of information which contributes to whether a behavior will be elicited. It appears to be the area in which motivation originates and the salience of stimuli are determined.[8]
  • The basolateral amygdala projects into the NAcc and is thought to be important for motivation as well.[8]
  • More evidence is pointing towards the role of the hippocampus in drug addiction because of its importance in learning and memory. Much of this evidence stems from investigations manipulating cells in the hippocampus alters dopamine levels in NAcc and firing rates of VTA dopaminergic cells.[5]

Stress response

In addition to the reward circuit, it is hypothesized that stress mechanisms also play a role in addiction. Koob and Kreek have hypothesized that during drug use corticotropin-releasing factor (CRF) activates the hypothalamic-pituitary-adrenal axis (HPA) and other stress systems in the extended amygdala. This activation influences the dysregulated emotional state associated with drug addiction. They have found that as drug use escalates, so does the presence of CRF in human cerebrospinal fluid (CSF). In rat models, the separate use of CRF antagonists and CRF receptor antagonists both decreased self-administration of the drug of study. Other studies in this review showed a dysregulation in other hormones associated with the HPA axis, including enkephalin which is an endogenous opioid peptides that regulates pain. It also appears that the µ-opioid receptor system, which enkephalin acts on, is influential in the reward system and can regulate the expression of stress hormones.[1]

File:Rational scale to assess the harm of drugs (mean physical harm and mean dependence).svg

Comparison of the perceived harm for various psychoactive drugs from a poll among medical psychiatrists specialized in addiction treatment[9]

Behavior

Understanding how learning and behavior work in the reward circuit can help understand the action of addictive drugs. Drug addiction is characterized by strong, drug seeking behaviors in which the addict persistently craves and seeks out drugs, despite the knowledge of harmful consequences.[3][1] Addictive drugs produce a reward, which is the euphoric feeling resulting from sustained DA concentrations in the synaptic cleft of neurons in the brain. Operant conditioning is exhibited in drug addicts as well as laboratory mice, rats, and primates; they are able to associate an action or behavior, in this case seeking out the drug, with a reward, which is the effect of the drug.[4] Evidence shows that this behavior is most likely a result of the synaptic changes which have occurred due to repeated drug exposure.[3][1][4] The drug seeking behavior is induced by glutamatergic projections from the prefrontal cortex to the NAc. This idea is supported with data from experiments showing the drug seeking behavior can be prevented following the inhibition of AMPA glutamate receptors and glutamate release in the NAc.[3]

Allostasis

Allostasis is the process of achieving stability through changes in behavior as well as physiological features. As a person progresses into drug addiction, he or she appears to enter a new allostatic state, defined as divergence from normal levels of change which persist in a chronic state. Addiction to drugs can cause damage to your brain and body as you enter the pathological state; the cost stemming from damage is known as allostatic load. The dysregulation of allostasis gradually occurs as the reward from the drug decreases and the ability to overcome the depressed state following drug use begins to decrease as well. The resulting allostatic load creates a constant state of depression relative to normal allostatic changes. What pushes this decrease is the propensity of drug users to take the drug before the brain and body have returned to original allostatic levels, producing a constant state of stress. Therefore, the presence of environmental stressors may induce stronger drug seeking behaviors.[1]

Neuroplasticity

Neuroplasticity is the putative mechanism behind learning and memory. It involves physical changes in the synapses between two communicating neurons, characterized by increased gene expression, altered cell signaling, and the formation of new synapses between the communicating neurons. When addictive drugs are present in the system, they appear to hijack this mechanism in the reward system so that motivation is geared towards procuring the drug rather than natural rewards.[4] Depending on the history of drug use, excitatory synapses in the nucleus accumbens(NAc) experience two types of neuroplasticity: long-term potentiation (LTP) and long-term depression (LTD). Using mice as a model, Kourrich et al. showed that chronic exposure to cocaine increases the strength of synapses in NAc after a 10-14 day withdrawal period, while strengthened synapses did not appear within a 24 hour withdrawal period after repeated cocaine exposure. A single dose of cocaine did not elicit any attributes of a strengthened synapse. When drug-experienced mice were challenged with one dose of cocaine, synaptic depression occurred. Therefore, it seems the history of cocaine exposure along with withdrawal times affects the direction of glutamatergic plasticity in the NAc.[7]

Once a person has transitioned from drug use to addiction, behavior becomes completely geared towards seeking the drug, even though addicts report the euphoria is not as intense as it once was. Despite the differing actions of drugs during acute use, the final pathway of addiction is the same. Another aspect of drug addiction is a decreased response to normal biological stimuli, such as food, sex, and social interaction. Through functional brain imaging of patients addicted to cocaine, scientists have been able to visualize increased metabolic activity in the anterior cingulate and orbitofrontal cortex (areas of the prefrontal cortex) in the brain of these subjects. The hyperactivity of these areas of the brain in addicted subjects is involved in the more intense motivation to find the drug rather than seeking natural rewards, as well as an addict’s decreased ability to overcome this urge. Brain imaging has also shown cocaine-addicted subjects to have decreased activity, as compared to non-addicts, in their prefrontal cortex when presented with stimuli associated with natural rewards. The transition from recreational drug use to addiction occurs in gradual stages and is produced by the effect of the drug of choice on the neuroplasticity of the neurons found in the reward circuit. During events preceding addiction, cravings are produced by the release of DA in the prefrontal cortex. As a person transitions from drug use to addiction, the release of dopamine (DA) in the NAc becomes unnecessary to produce cravings; rather, DA transmission decreases while increased metabolic activity in the orbitofrontal cortex contributes to cravings. At this time a person may experience the signs of depression if cocaine is not used. [10] Before a person becomes addicted and exhibits drug-seeking behavior, there is a time period in which the neuroplasticity is reversible. Addiction occurs when drug-seeking behavior is exhibited and the vulnerability to relapse persists, despite prolonged withdrawal; these behavioral attributes are the result of neuroplastic changes which are brought about by repeated exposure to drugs and are relatively permanent.[3]

The exact mechanism behind a drug molecule’s effect on synaptic plasticity is still unclear. However, neuroplasticity in glutamatergic projections seems to be a major result of repeated drug exposure. There are several ways in which glutamate transmission is altered. One way is by increasing presynaptic release of glutamate and the other is increased response to glutamate.[3][4] The two main glutamate receptors involved are NMDAR and AMPAR. The expression of these receptors on the cell surface increases with repeated drug use. This type of synaptic plasticity results in LTP, which strengthens connections between two neurons; onset of this occurs quickly and the result is constant. In addition to glutamatergic neurons, dopaminergic neurons present in the VTA respond to glutamate and may be recruited earliest during neural adaptations caused by repeated drug exposure. As shown by Kourrich, et al, history of drug exposure and the time of withdrawal from last exposure appear to play an important role in the direction of plasticity in the neurons of the reward system.[4]

An aspect of neuron development that may also play a part in drug-induced neuroplasticity is the presence of axon guidance molecules such as semaphorins and ephrins. After repeated cocaine treatment, altered expression (increase or decrease dependent on the type of molecule) of mRNA coding for axon guidance molecules occurred in rats. This may contribute to the alterations in the reward circuit characteristic of drug addiction.[11]

Neurogenesis

Drug addiction also raises the issue of potential harmful effects on the development of new neurons in adults. Eisch and Harburg raise three new concepts they have extrapolated from the numerous recent studies on drug addiction. First, neurogenesis decreases as a result of repeated exposure to addictive drugs. A list of studies show that chronic use of opiates, psychostimulants, nicotine, and alcohol decrease neurogenesis in mice and rats. Second, this apparent decrease in neurogenesis seems to be independent of HPA axis activation. Other environmental factors other than drug exposure such as age, stress and exercise, can also have an effect of neurogenesis by regulating the hypothalamic-pituitary-adrenal (HPA) axis. Mounting evidence suggests this for 3 reasons: small doses of opiates and psychostimulants increase coricosterone concentration in serum but with no effect of neurogenesis; although decreased neurogenesis is similar between self-administered and forced drug intake, activation of HPA axis is greater in self-administration subjects; and even after the inhibition of opiate induced increase of corticosterone, a decrease in neurogenesis occurred. These, of course, need to be investigated further. Last, addictive drugs appear to only affect proliferation in the subgranular zone (SGZ), rather than other areas associated with neurogenesis. The studies of drug use and neurogenesis may have implications on stem cell biology.[5]

Psychological drug tolerance

The reward system is partly responsible for the psychological part of drug tolerance;

The CREB protein, a transcription factor activated by cyclic adenosine monophosphate (cAMP) immediately after a high, triggers genes that produce proteins such as dynorphin, which cuts off dopamine release and temporarily inhibits the reward circuit. In chronic drug users, a sustained activation of CREB thus forces a larger dose to be taken to reach the same effect. In addition it leaves the user feeling generally depressed and dissatisfied, and unable to find pleasure in previously enjoyable activities, often leading to a return to the drug for an additional "fix".[12].

Sensitization

Sensitization is the increase in sensitivity to a drug after prolonged use. The proteins delta FosB and regulator of G-protein Signaling 9-2 (RGS 9-2) are thought to be involved:

A transcription factor, known as delta FosB, is thought to activate genes that, counter to the effects of CREB, actually increase the user's sensitivity to the effects of the substance. Delta FosB slowly builds up with each exposure to the drug and remains activated for weeks after the last exposure—long after the effects of CREB have faded. The hypersensitivity that it causes is thought to be responsible for the intense cravings associated with drug addiction, and is often extended to even the peripheral cues of drug use, such as related behaviors or the sight of drug paraphernalia. There is some evidence that delta FosB even causes structural changes within the nucleus accumbens, which presumably helps to perpetuate the cravings, and may be responsible for the high incidence of relapse that occur in treated drug addicts.

Regulator of G-protein Signaling 9-2 (RGS 9-2) has recently been the subject of several animal knockout studies. Animals lacking RGS 9-2 appear to have increased sensitivity to dopamine receptor agonists such as cocaine and amphetamines; over-expression of RGS 9-2 causes a lack of responsiveness to these same agonists. RGS 9-2 is believed to catalyze inactivation of the G-protein coupled D2 receptor by enhancing the rate of GTP hydrolysis of the G alpha subunit which transmits signals into the interior of the cell.

Individual mechanisms of effect

The basic mechanisms by which different substances activate the reward system are as described above, but vary slightly among drug classes.[13].

Depressants

Depressants such as alcohol and benzodiazepines work by increasing the affinity of the GABA receptor for its ligand; GABA. Narcotics such as morphine and methadone, work by mimicking endorphins—chemicals produced naturally by the body which have effects similar to dopamine—or by disabling the neurons that normally inhibit the release of dopamine in the reward system. These substances (sometimes called "downers") typically facilitate relaxation and pain-relief.

Stimulants

Stimulants such as amphetamines, nicotine, and cocaine, increase dopamine signaling in the reward system either by directly stimulating its release, or by blocking its absorption (see "reuptake"). These substances (sometimes called "uppers") typically cause heightened alertness and energy. They cause a pleasant feeling in the body, and euphoria, known as a high. This high wears off leaving the user feeling depressed. This sometimes makes them want more of the drug, and can worsen the addiction.

Theories about causes for epidemic outbreak of addiction

Nils Bejerot

Nils Bejerot (1921 –1988) was a Swedish psychiatrist and criminologist. He attacked the symptom theory of addiction - that addictions are a symptom of other more fundamental personal or socioeconomic problems - and separated five essential factors from all of the other factors that are involved in addiction. Bejerot's point was that all of these other factors should be understood as susceptibility or risk factors. Therefore mental illness may make someone susceptible to drug experimentation and use, but it is not a causal factor. Similarly, poverty may increase susceptibility, but there is no automatic causal relationship with addiction. Many poverty-stricken communities are free of addiction epidemics, as are many people with mental illness.

Bejerot's analysis was that the presence of five factors on their own constitutes a risk that an individual will become an addict, or that a community will be affected by an epidemic of addiction:

  • Availability of the addictive substance
  • Money to acquire the substance
  • Time to use the substance
  • Example of use of the substance in the immediate environment
  • A permissive ideology in relation to the use of the substance. [14]

Bejerot's opinion was that drug addicts must be prosecuted. This does not mean that Bejerot proposed what he called the harsh American sentences. - The society must (in his view), however, make it very uncomfortable to abuse illicit drugs. [15] Drug addict should be offered treatment, mandatory if necessary, but not treatment that helped them to continue the abuse of the drug.

Treatment

Treatments for drug addiction vary widely according to the types of drugs involved, amount of drugs used, duration of the drug addiction, medical complications and the social needs of the individual.

Determining the best type of recovery program for an addicted person depends on a number of factors, including: personality, drug(s) of addiction, concept of spirituality or religion, mental or physical illness, and local availability and affordability of programs.

Many different ideas circulate regarding what is considered a "successful" outcome in the recovery from addiction. It has widely been established that abstinence from addictive substances is generally accepted as a "successful" outcome, however differences of opinion exist as to the extent of abstinence required.

In the USA and in many other countries, the goal of treatment for drug dependence is generally total abstinence from all drugs, which while theoretically the ideal outcome, is in practice often very difficult to achieve. Other countries particularly in Europe argue the aims of treatment for drug dependence to be more complex, with treatment aims including reduction in use to the point that drug use no longer interferes with normal activities such as work and family commitments, shifts away from more dangerous routes of drug administration such as injecting to safer routes such as oral administration, reduction in crime committed by drug addicts, and treatment of other comorbid conditions such as AIDS, hepatitis and mental health disorders. These kind of outcomes can often be achieved without necessarily eliminating drug use completely, and so drug treatment programs in Europe often report more favourable outcomes than those in the USA because the criteria for measuring success can be met even though drug users on the programme may still be using drugs to some extent.[16][17][18] The supporters of programs with total abstinence from drugs as a goal stress that enabling further drug use mean prolonged drug use and a risk for an increase of total number of addicts; the participants in the program can introduce new users in the habit. [19]


Drug addiction is a complex but treatable brain disease. It is characterized by compulsive drug craving, seeking, and use that persist even in the face of severe adverse consequences. For many people, drug addiction becomes chronic, with relapses possible even after long periods of abstinence. In fact, relapse to drug abuse occurs at rates similar to those for other well-characterized, chronic medical illnesses such as diabetes, hypertension, and asthma. As a chronic, recurring illness, addiction may require repeated treatments to increase the intervals between relapses and diminish their intensity, until abstinence is achieved. Through treatment tailored to individual needs, people with drug addiction can recover and lead productive lives. The ultimate goal of drug addiction treatment is to enable an individual to achieve lasting abstinence, but the immediate goals are to reduce drug abuse, improve the patient's ability to function, and minimize the medical and social complications of drug abuse and addiction. Like people with diabetes or heart disease, people in treatment for drug addiction will need to change behavior to adopt a more healthful lifestyle.[20]

Residential

Residential drug treatment can be broadly divided into two camps: 12 step programs or Therapeutic Communities. 12 step programs have the advantage of coming with an instant social support network though some find the spiritual context not to their taste. In the UK drug treatment is generally moving towards a more integrated approach with rehabs offering a variety of approaches. These other programs may use Cognitive-Behavioral Therapy an approach that looks at the relationship between thoughts feelings and behaviors, recognizing that a change in any of these areas can affect the whole. CBT sees addiction as a behavior rather than a disease and subsequently curable, or rather, unlearnable. CBT programs recognize that for some individuals controlled use is a more realistic possibility. [21]

12 step program

One of many recovery methods is the 12 step recovery program, with prominent examples including Alcoholics Anonymous and Narcotics Anonymous. They are commonly known and used for a variety of addictions for the individual addicted and the family of the individual. Substance-abuse rehabilitation (or "rehab") centers frequently offer a residential treatment program for the seriously addicted in order to isolate the patient from drugs and interactions with other users and dealers. Outpatient clinics usually offer a combination of individual counseling and group counseling. Frequently a physician or psychiatrist will assist with prescriptions to assist with the side effects of the addiction (the most common side effect that the medications can help is anxiety).

Anti-addictive drugs

Other forms of treatment include replacement drugs such as methadone or buprenorphine, used as a substitute for illicit opiate drugs.[22][23] Although these drugs are themselves addictive, opioid dependency is often so strong that a way to stabilize levels of opioid needed and a way to gradually reduce the levels of opioid needed are required. In some countries, other opioid derivatives such as levomethadyl acetate,[24] dihydrocodeine,[25] dihydroetorphine[26] and even heroin[27][28] are used as substitute drugs for illegal street opiates, with different drugs being used depending on the needs of the individual patient.[29]

Substitute drugs for other forms of drug dependence have historically been less successful than opioid substitute treatment, but some limited success has been seen with drugs such as dexamphetamine to treat stimulant addiction,[30][31] and clomethiazole to treat alcohol addiction.[32] Bromocriptine and desipramine have been reported to be effective for treatment of cocaine but not amphetamine addiction.[33]

Other pharmacological treatments for alcohol addiction include drugs like disulfiram, acamprosate and topiramate,[34][35] but rather than substituting for alcohol, these drugs are intended to reduce the desire to drink, either by directly reducing cravings as with acamprosate and topiramate, or by producing unpleasant effects when alcohol is consumed, as with disulfiram. These drugs can be effective if treatment is maintained, but compliance can be an issue as alcoholic patients often forget to take their medication, or discontinue use because of excessive side effects.[36][37] Additional drugs acting on glutamate neurotransmission such as modafinil, lamotrigine, gabapentin and memantine have also been proposed for use in treating addiction to alcohol and other drugs.[38]

Opioid antagonists such as naltrexone and nalmefene have also been used successfully in the treatment of alcohol addiction,[39][40] which is often particularly challenging to treat. These drugs have also been used to a lesser extent for long-term maintenance treatment of former opiate addicts, but cannot be started until the patient has been abstinent for an extended period, otherwise they can trigger acute opioid withdrawal symptoms.[41]

Treatment of stimulant addiction can often be difficult, with substitute drugs often being ineffective, although newer drugs such as nocaine, vanoxerine and modafinil may have more promise in this area, as well as the GABAB agonist baclofen.[42][43] Another strategy that has recently been successfully trialled used a combination of the benzodiazepine antagonist flumazenil with hydroxyzine and gabapentin for the treatment of methamphetamine addiction.[44]

Another area in which drug treatment has been widely used is in the treatment of nicotine addiction. Various drugs have been used for this purpose such as bupropion, mecamylamine and the more recently developed varenicline. The cannaboinoid antagonist rimonabant has also been trialled for treatment of nicotine addiction but has not been widely adopted for this purpose.[45][46][47]

Ibogaine is a psychoactive drug that specifically interrupts the addictive response, and is currently being studied for its effects upon cocaine, heroin, nicotine, and SSRI addicts. Alternative medicine clinics offering ibogaine treatment have appeared along the U.S. border.[48] Ibogaine treatment for drug addiction can be reasonably effective, but potentially dangerous side effects which have been linked to several deaths have limited its adoption by conventional medical practice.[49] A synthetic analogue of ibogaine, 18-methoxycoronaridine has also been developed which has similar efficacy but less side effects, however this drug is still being tested in animals and human trials have not yet been carried out.[50][51]

Alternative therapies

Alternative therapies, such as acupuncture, are used by some practitioners to alleviate the symptoms of drug addiction. In 1997, the American Medical Association (AMA) adopted as policy the following statement after a report on a number of alternative therapies including acupuncture:

There is little evidence to confirm the safety or efficacy of most alternative therapies. Much of the information currently known about these therapies makes it clear that many have not been shown to be efficacious. Well-designed, stringently controlled research should be done to evaluate the efficacy of alternative therapies.

Acupuncture has been shown to be no more effective than control treatments in the treatment of opiate dependence.[52] Acupuncture, acupressure, laser therapy and electrostimulation have no demonstrated efficacy for smoking cessation.[53]

Medical definitions

The terms abuse and addiction have been defined and re-defined over the years. The 1957 World Health Organization (WHO) Expert Committee on Addiction-Producing Drugs defined addiction and habituation as components of drug abuse:

Drug addiction is a state of periodic or chronic intoxication produced by the repeated consumption of a drug (natural or synthetic). Its characteristics include: (i) an overpowering desire or need (compulsion) to continue taking the drug and to obtain it by any means; (ii) a tendency to increase the dose; (iii) a psychic (psychological) and generally a physical dependence on the effects of the drug; and (iv) detrimental effects on the individual and on society.

Drug habituation (habit) is a condition resulting from the repeated consumption of a drug. Its characteristics include (i) a desire (but not a compulsion) to continue taking the drug for the sense of improved well-being which it engenders; (ii) little or no tendency to increase the dose; (iii) some degree of psychic dependence on the effect of the drug, but absence of physical dependence and hence of an abstinence syndrome [withdrawal], and (iv) detrimental effects, if any, primarily on the individual.

In 1964, a new WHO committee found these definitions to be inadequate, and suggested using the blanket term "drug dependence":

The definition of addiction gained some acceptance, but confusion in the use of the terms addiction and habituation and misuse of the former continued. Further, the list of drugs abused increased in number and diversity. These difficulties have become increasingly apparent and various attempts have been made to find a term that could be applied to drug abuse generally. The component in common appears to be dependence, whether psychic or physical or both. Hence, use of the term 'drug dependence', with a modifying phase linking it to a particular drug type in order to differentiate one class of drugs from another, had been given most careful consideration. The Expert Committee recommends substitution of the term 'drug dependence' for the terms 'drug addiction' and 'drug habituation'.

The committee did not clearly define dependence, but did go on to clarify that there was a distinction between physical and psychological ("psychic") dependence. It said that drug abuse was "a state of psychic dependence or physical dependence, or both, on a drug, arising in a person following administration of that drug on a periodic or continued basis." Psychic dependence was defined as a state in which "there is a feeling of satisfaction and psychic drive that requires periodic or continuous administration of the drug to produce pleasure or to avoid discomfort" and all drugs were said to be capable of producing this state:

There is scarcely any agent which can be taken into the body to which some individuals will not get a reaction satisfactory or pleasurable to them, persuading them to continue its use even to the point of abuse — that is, to excessive or persistent use beyond medical need.

The 1957 and 1964 definitions of addiction, dependence and abuse persist to the present day in medical literature. It should be noted that at this time (2006) the Diagnostic Statistical Manual (DSM IVR) now spells out specific criteria for defining abuse and dependence. (DSM IVR) uses the term substance dependence instead of addiction; a maladaptive pattern of substance abuse, leading to clinically significant impairment or distress, as manifested by three (or more) specified criteria, occurring at any time in the same 12-month period. This definition is also applicable on drugs with smaller or nonexistent physical signs of withdrawal, for ex. cannabis.

In 2001, the American Academy of Pain Medicine, the American Pain Society, and the American Society of Addiction Medicine jointly issued "Definitions Related to the Use of Opioids for the Treatment of Pain," which defined the following terms:[2]

Addiction is a primary, chronic, neurobiologic disease, with genetic, psychosocial, and environmental factors influencing its development and manifestations. It is characterized by behaviors that include one or more of the following: impaired control over drug use, compulsive use, continued use despite harm, and craving.

Physical dependence is a state of adaptation that is manifested by a drug class specific withdrawal syndrome that can be produced by abrupt cessation, rapid dose reduction, decreasing blood level of the drug, and/or administration of an antagonist.

Tolerance is the body's physical adaptation to a drug: greater amounts of the drug are required over time to achieve the initial effect as the body "gets used to" and adapts to the intake.

Pseudo addiction is a term which has been used to describe patient behaviors that may occur when pain is undertreated. Patients with unrelieved pain may become focused on obtaining medications, may “clock watch,” and may otherwise seem inappropriately “drug seeking.” Even such behaviors as illicit drug use and deception can occur in the patient's efforts to obtain relief. Pseudoaddiction can be distinguished from true addiction in that the behaviors resolve when pain is effectively treated.

The Diagnostic and Statistical Manual of Mental Disorders, DSM-IV-TR doesn’t use the word addiction at all. Instead it has a section about Substance dependence

"When an individual persists in use of alcohol or other drugs despite problems related to use of the substance, substance dependence may be diagnosed. Compulsive and repetitive use may result in tolerance to the effect of the drug and withdrawal symptoms when use is reduced or stopped. This, along with Substance Abuse are considered Substance Use Disorders...." [54]

A definition of addiction proposed by professor Nils Bejerot:

"An emotional fixation (sentiment) acquired through learning, which intermittently or continually expresses itself in purposeful, stereotyped behavior with the character and force of a natural drive, aiming at a specific pleasure or the avoidance of a specific discomfort."[55]

Addiction and drug control legislation

Depending on the jurisdiction, addictive drugs may be legal only as part of a government sponsored study, illegal to use for any purpose, illegal to sell, or even illegal to merely possess.

Most countries have legislation which brings various drugs and drug-like substances under the control of licensing systems. Typically this legislation covers any or all of the opiates, amphetamines, cannabinoids, cocaine, barbiturates, hallucinogenics and a variety of more modern synthetic drugs, and unlicensed production, supply or possession is a criminal offence.

Usually, however, drug classification under such legislation is not related simply to addictiveness. The substances covered often have very different addictive properties. Some are highly prone to cause physical dependency, whilst others rarely cause any form of compulsive need whatsoever. Also, under legislation specifically about drugs, alcohol is not usually included.

Although the legislation may be justifiable on moral or public health grounds, it can make addiction or dependency a much more serious issue for the individual: reliable supplies of a drug become difficult to secure, and the individual becomes vulnerable to both criminal abuse and legal punishment.

It is unclear whether laws against drugs do anything to stem usage and dependency. In jurisdictions where addictive drugs are illegal, they are generally supplied by drug dealers, who are often involved with organized crime. Even though the cost of producing most illegal addictive substances is very low, their illegality combined with the addict's need permits the seller to command a premium price, often hundreds of times the production cost. As a result, the addict sometimes turns to crime to support their habit.

History of addiction

The phenomenon of drug addiction has occurred to some degree throughout recorded history (see "opium"). Modern agricultural practices, improvements in access to drugs, advancements in biochemistry, and dramatic increases in the recommendation of drug usage by clinical practitioners have exacerbated the problem significantly in the 20th century. Improved means of active biological agent manufacture and the introduction of synthetic compounds, such as methamphetamine are also factors contributing to drug addiction.[56]

See also

Literature

  • Sainsbury, Drug and the Drug Habit (New York, 1909)
  • C. A. McBride, Modern Treatment of Alcoholism and Drug Narcotism (New York, 1910)
  • G. E. Pettey, Narcotic Drug Diseases and Allied Ailments (Philadelphia, 1913)
  • Fitz Hugh Ludlow wrote The Hasheesh Eater (1857) and The Opium Habit (1868), designed as a warning.
  • Thomas de Quincey, Confessions of an English Opium Eater (London, 1822)
  • William S. Burroughs, Junkie (New York, 1953)

References

  1. 1.0 1.1 1.2 1.3 1.4 Koob G, Kreek MJ (2007). Stress, dysregulation of drug reward pathways, and the transition to drug dependence. Am J Psychiatry 164 (8): 1149–59.
  2. 2.0 2.1 2001 "Definitions Related to the Use of Opioids for the Treatment of Pain,", the American Academy of Pain Medicine, the American Pain Society, and the American Society of Addiction Medicine
  3. 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Kalivas PW, Volkow ND (2005). The neural basis of addiction: a pathology of motivation and choice. Am J Psychiatry 162 (8): 1403–13.
  4. 4.0 4.1 4.2 4.3 4.4 4.5 4.6 Jones S, Bonci A (2005). Synaptic plasticity and drug addiction. Curr Opin Pharmacol 5 (1): 20–5.
  5. 5.0 5.1 5.2 Eisch AJ, Harburg GC (2006). Opiates, psychostimulants, and adult hippocampal neurogenesis: Insights for addiction and stem cell biology. Hippocampus 16 (3): 271–86.
  6. Rang, H. P. (2003). Pharmacology, page 596, Edinburgh: Churchill Livingstone.
  7. 7.0 7.1 Kourrich S, Rothwell PE, Klug JR, Thomas MJ (2007). Cocaine experience controls bidirectional synaptic plasticity in the nucleus accumbens. J. Neurosci. 27 (30): 7921–8.
  8. 8.0 8.1 Floresco SB, Ghods-Sharifi S (2007). Amygdala-prefrontal cortical circuitry regulates effort-based decision making. Cereb. Cortex 17 (2): 251–60.
  9. Nutt D, King LA, Saulsbury W, Blakemore C (2007). Development of a rational scale to assess the harm of drugs of potential misue. Lancet 369 (9566): 1047–53.
  10. AJ Giannini. Drug abuse and depression: Catecholamine depletion suggested as biological tie between cocaine withdrawal and depression. National Institute of Drug Abuse Notes. 2(2)5, 1987.
  11. Bahi A, Dreyer JL (2005). Cocaine-induced expression changes of axon guidance molecules in the adult rat brain. Mol. Cell. Neurosci. 28 (2): 275–91.
  12. AJ Giannini. RQ Quinones, DM Martin. Role of beta-endorphin and cAMP in addiction and mania. Society for Neuroscience Abstracts.15:149,1998.
  13. NS Miller, AJ Giannini. The disease model of addiction. Journal of Psychoactive Drugs.22(1):83-85,1990
  14. Noel Pearson: Agendas of addiction, 2008
  15. Nils Bejerot: Swedish addiction epidemic in an international perspective, 1988
  16. Ball JC, van de Wijngaart GF (1994). A Dutch addict's view of methadone maintenance--an American and a Dutch appraisal. Addiction 89 (7): 799–802; discussion 803–14.
  17. Reynolds M, Mezey G, Chapman M, Wheeler M, Drummond C, Baldacchino A (2005). Co-morbid post-traumatic stress disorder in a substance misusing clinical population. Drug Alcohol Depend 77 (3): 251–8.
  18. Moggi F, Giovanoli A, Strik W, Moos BS, Moos RH (2007). Substance use disorder treatment programs in Switzerland and the USA: Program characteristics and 1-year outcomes. Drug Alcohol Depend 86 (1): 75–83.
  19. {http://www.rns.se/swedish-addiction.asp Nils Bejerot: The Swedish Addiction Epidemic in global perspective]
  20. InfoFacts - Treatment Approaches for Drug Addiction
  21. AJ Giannini. Alexythymia,affective disorders and substance abuse:possible cross relationships. Psychological Reports.78:1389-1391, 1996.
  22. Johnson RE, Chutuape MA, Strain EC, Walsh SL, Stitzer ML, Bigelow GE (2000). A comparison of levomethadyl acetate, buprenorphine, and methadone for opioid dependence. N. Engl. J. Med. 343 (18): 1290–7.
  23. Connock M, Juarez-Garcia A, Jowett S, et al (2007). Methadone and buprenorphine for the management of opioid dependence: a systematic review and economic evaluation. Health Technol Assess 11 (9): 1–171, iii–iv.
  24. Marsch LA, Stephens MA, Mudric T, Strain EC, Bigelow GE, Johnson RE (2005). Predictors of outcome in LAAM, buprenorphine, and methadone treatment for opioid dependence. Exp Clin Psychopharmacol 13 (4): 293–302.
  25. Robertson JR, Raab GM, Bruce M, McKenzie JS, Storkey HR, Salter A (2006). Addressing the efficacy of dihydrocodeine versus methadone as an alternative maintenance treatment for opiate dependence: A randomized controlled trial. Addiction 101 (12): 1752–9.
  26. Qin Bo-Yi (1998). Advances in dihydroetorphine: From analgesia to detoxification. Drug Development Research 39 (2): 131–134. Link
  27. Metrebian N, Shanahan W, Wells B, Stimson GV (1998). Feasibility of prescribing injectable heroin and methadone to opiate-dependent drug users: associated health gains and harm reductions. Med. J. Aust. 168 (12): 596–600.
  28. Metrebian N, Mott J, Carnwath Z, Carnwath T, Stimson GV, Sell L (2007). Pathways into receiving a prescription for diamorphine (heroin) for the treatment of opiate dependence in the United kingdom. Eur Addict Res 13 (3): 144–7.
  29. Kenna GA, Nielsen DM, Mello P, Schiesl A, Swift RM (2007). Pharmacotherapy of dual substance abuse and dependence. CNS Drugs 21 (3): 213–37.
  30. Mattick RP, Darke S (1995). Drug replacement treatments: is amphetamine substitution a horse of a different colour?. Drug Alcohol Rev 14 (4): 389–94.
  31. White R (2000). Dexamphetamine substitution in the treatment of amphetamine abuse: an initial investigation. Addiction 95 (2): 229–38.
  32. Majumdar SK (1991). Chlormethiazole: current status in the treatment of the acute ethanol withdrawal syndrome. Drug Alcohol Depend 27 (3): 201–7.
  33. AJ Giannini,TA Billet. Bromocriptine-desipramine protocol in cocaine detoxification. Journal of Clinical Pharmacology. 27:549-554,1987.
  34. Soyka M, Roesner S (2006). New pharmacological approaches for the treatment of alcoholism. Expert Opin Pharmacother 7 (17): 2341–53.
  35. Pettinati HM, Rabinowitz AR (2006). Choosing the right medication for the treatment of alcoholism. Curr Psychiatry Rep 8 (5): 383–8.
  36. Bouza C, Angeles M, Magro A, Muñoz A, Amate JM (2004). Efficacy and safety of naltrexone and acamprosate in the treatment of alcohol dependence: a systematic review. Addiction 99 (7): 811–28.
  37. Williams SH (2005). Medications for treating alcohol dependence. Am Fam Physician 72 (9): 1775–80.
  38. Gass JT, Olive MF (2008). Glutamatergic substrates of drug addiction and alcoholism. Biochem. Pharmacol. 75 (1): 218–65.
  39. Srisurapanont M, Jarusuraisin N (2005). Opioid antagonists for alcohol dependence. Cochrane Database Syst Rev (1): CD001867.
  40. Karhuvaara S, Simojoki K, Virta A, et al (2007). Targeted nalmefene with simple medical management in the treatment of heavy drinkers: a randomized double-blind placebo-controlled multicenter study. Alcohol. Clin. Exp. Res. 31 (7): 1179–87.
  41. Comer SD, Sullivan MA, Hulse GK (2007). Sustained-release naltrexone: novel treatment for opioid dependence. Expert Opin Investig Drugs 16 (8): 1285–94.
  42. Ling W, Rawson R, Shoptaw S, Ling W (2006). Management of methamphetamine abuse and dependence. Curr Psychiatry Rep 8 (5): 345–54.
  43. Preti A (2007). New developments in the pharmacotherapy of cocaine abuse. Addict Biol 12 (2): 133–51.
  44. Urschel HC, Hanselka LL, Gromov I, White L, Baron M (2007). Open-label study of a proprietary treatment program targeting type A gamma-aminobutyric acid receptor dysregulation in methamphetamine dependence. Mayo Clin. Proc. 82 (10): 1170–8.
  45. Garwood CL, Potts LA (2007). Emerging pharmacotherapies for smoking cessation. Am J Health Syst Pharm 64 (16): 1693–8.
  46. Frishman WH (2007). Smoking cessation pharmacotherapy--nicotine and non-nicotine preparations. Prev Cardiol 10 (2 Suppl 1): 10–22.
  47. Siu EC, Tyndale RF (2007). Non-nicotinic therapies for smoking cessation. Annu. Rev. Pharmacol. Toxicol. 47: 541–64.
  48. Alper KR, Lotsof HS, Kaplan CD (2008). The ibogaine medical subculture. J Ethnopharmacol 115 (1): 9–24.
  49. Mash DC, Kovera CA, Pablo J, et al (2000). Ibogaine: complex pharmacokinetics, concerns for safety, and preliminary efficacy measures. Ann. N. Y. Acad. Sci. 914: 394–401.
  50. Levi MS, Borne RF (2002). A review of chemical agents in the pharmacotherapy of addiction. Curr. Med. Chem. 9 (20): 1807–18.
  51. Werneke U, Turner T, Priebe S (2006). Complementary medicines in psychiatry: review of effectiveness and safety. Br J Psychiatry 188: 109–21.
  52. Jordan JB (2006). Acupuncture treatment for opiate addiction: a systematic review. J Subst Abuse Treat 30 (4): 309–14.
  53. White AR, Rampes H, Campbell JL (2006). Acupuncture and related interventions for smoking cessation. Cochrane Database Syst Rev (1): CD000009.
  54. DSM-IV & DSM-IV-TR:Substance Dependence
  55. Nils Bejerot in Theories of Drug abuse, Selected contemporary perspectives, page 246-255, NIDA, 1980
  56. DCA Hillman. The Chemical Muse. New York City,St. Martin's Press,2008

Sources

External links

{{{2}}} at the Open Directory Project

[[Category:Side effects (drug)


This page uses Creative Commons Licensed content from Wikipedia (view authors).