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Dopamine
Dopamine2
Dopamine-3d-CPK
General
Systematic name 4-(2-aminoethyl)benzene-1,2-diol
Other names 2-(3,4-dihydroxyphenyl)ethylamine;
3,4-dihydroxyphenethylamine;
3-hydroxytyramine; DA; Intropin
Revivan; Oxytyramine
Molecular formula C8H11NO2
SMILES NCCc1ccc(O)c(O)c1
Molar mass 153.178 g/mol
Appearance white powder with distinctive smell
CAS number [51-61-6]
Properties
Density and phase  ? g/cm³, ?
Solubility in water 60.0 g/100 ml (? °C), solid
Melting point 128 °C (401 K)
Boiling point  ? °C (? K)
Acidity (pKa)  ?
Basicity (pKb)  ?
Chiral rotation [α]D  ?°
Viscosity  ? cP at ? °C
Structure
Molecular shape  ?
Coordination
geometry
 ?
Crystal structure  ?
Dipole moment  ? D
Hazards
MSDS External MSDS
Main hazards  ?
NFPA 704  ?
Flash point  ? °C
R/S statement R: 36/37/38
S: 26-36
RTECS number UX1088000
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Related compounds
Other anions  ?
Other cations  ?
Related Tyramine,
octopamine,
norepinephrine (noradrenaline)
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)
Infobox disclaimer and references

Dopamine is a hormone and neurotransmitter occurring in a wide variety of animals, including both vertebrates and invertebrates. In chemical structure, it is a phenethylamine.

In the brain, dopamine functions as a neurotransmitter, activating the five types of dopamine receptors — D1, D2, D3, D4 and D5, and their variants. Dopamine is produced in several areas of the brain, including the substantia nigra. Dopamine is also a neurohormone released by the hypothalamus. Its main function as a hormone is to inhibit the release of prolactin from the anterior lobe of the pituitary.

Dopamine can be supplied as a medication that acts on the sympathetic nervous system, producing effects such as increased heart rate and blood pressure. However, because dopamine cannot cross the blood-brain barrier, dopamine given as a drug does not directly affect the central nervous system. To increase the amount of dopamine in the brains of patients with diseases such as Parkinson's disease and Dopa-Responsive dystonia, L-DOPA (levodopa), which is the precursor of dopamine, can be given because it can cross the blood-brain barrier.

History Edit

Dopamine was discovered by Arvid Carlsson and Nils-Åke Hillarp at the Laboratory for Chemical Pharmacology of the National Heart Institute of Sweden, in 1952. It was named Dopamine because it was a monoamine, and its synthetic precursor was 3,4-dihydroxyphenylalanine (L-DOPA).[1] Arvid Carlsson was awarded the 2000 Nobel Prize in Physiology or Medicine for showing that dopamine is not just a precursor of norepinephrine (noradrenaline) and epinephrine (adrenaline) but a neurotransmitter, as well.

Dopamine was first synthesized artificially in 1910 by George Barger and James Ewens at Wellcome Laboratories in London, England.[2]

Biochemistry Edit

File:Catecholamines biosynthesis.svg

Name and family Edit

Dopamine has the chemical formula C6H3(OH)2-CH2-CH2-NH2. Its chemical name is "4-(2-aminoethyl)benzene-1,2-diol" and its abbreviation is "DA."

As a member of the catecholamine family, dopamine is a precursor to norepinephrine (noradrenaline) and then epinephrine (adrenaline) in the biosynthetic pathways for these neurotransmitters.

Biosynthesis Edit

Dopamine is biosynthesized in the body (mainly by nervous tissue and the medulla of the adrenal glands) first by the hydration of the amino acid L-tyrosine to L-DOPA via the enzyme tyrosine 3-monooxygenase, also known as tyrosine hydroxylase, and then by the decarboxylation of L-DOPA by aromatic L-amino acid decarboxylase (which is often referred to as dopa decarboxylase). In some neurons, dopamine is further processed into norepinephrine by dopamine beta-hydroxylase.

In neurons, dopamine is packaged after synthesis into vesicles, which are then released into the synapse in response to a presynaptic action potential.

Inactivation and degradation Edit

Dopamine degradation

Dopamine is inactivated by reuptake via the dopamine transporter, then enzymatic breakdown by catechol-O-methyl transferase (COMT) and monoamine oxidase (MAO). Dopamine that is not broken down by enzymes is repackaged into vesicles for reuse.

Dopamine may also simply diffuse away from the synapse, and help to regulate blood pressure.

Functions in the brainEdit

Dopamine has many functions in the brain, including important roles in behavior and cognition, motor activity, motivation and reward, regulation of milk production, sleep, mood, attention, and learning. Dopaminergic neurons (i.e., neurons whose primary neurotransmitter is dopamine) are present chiefly in the ventral tegmental area (VTA) of the midbrain, substantia nigra pars compacta, and arcuate nucleus of the hypothalamus.

The phasic responses of dopamine neurons are observed when an unexpected reward is presented. These responses transfer to the onset of a conditioned stimulus after repeated pairings with the reward. Further, dopamine neurons are depressed when the expected reward is omitted. Thus, dopamine neurons seem to encode the prediction error of rewarding outcomes. In nature, we learn to repeat behaviors that lead to maximize rewards. Dopamine is therefore believed to provide a teaching signal to parts of the brain responsible for acquiring new behavior. Temporal difference learning provides a computational model describing how the prediction error of dopamine neurons is used as a teaching signal.

In insects, a similar reward system exists, using octopamine, a chemical relative of dopamine.[3]

Anatomy Edit

Dopaminergic neurons form a neurotransmitter system which originates in substantia nigra pars compacta, ventral tegmental area (VTA) and hypothalamus. These project axons to large areas of the brain through some major pathways:

This innervation explains many of the effects of activating this dopamine system. For instance, the mesolimbic pathway connects the VTA and nucleus accumbens, both are central to the brain reward system.[4]

Movement Edit

Via the dopamine receptors D1, D2, D3, D4 and D5, dopamine reduces the influence of the indirect pathway, and increases the actions of the direct pathway within the basal ganglia. Insufficient dopamine biosynthesis in the dopaminergic neurons can cause Parkinson's disease, in which a person loses the ability to execute smooth, controlled movements. The phasic dopaminergic activation seems to be crucial with respect to a lasting internal encoding of motor skills (Beck, 2005).

Cognition and frontal cortex Edit

In the frontal lobes, dopamine controls the flow of information from other areas of the brain. Dopamine disorders in this region of the brain can cause a decline in neurocognitive functions, especially memory, attention, and problem-solving. Reduced dopamine concentrations in the prefrontal cortex are thought to contribute to attention deficit disorder. On the converse, however, anti-psychotic medications act as dopamine antagonists and are used in the treatment of positive symptoms in schizophrenia.

Regulating prolactin secretion Edit

Dopamine is the primary neuroendocrine regulator of the secretion of prolactin from the anterior pituitary gland. Dopamine produced by neurons in the arcuate nucleus of the hypothalamus is secreted into the hypothalamo-hypophysial blood vessels of the median eminence, which supply the pituitary gland. The lactotrope cells that produce prolactin, in the absence of dopamine, secrete prolactin continuously; dopamine inhibits this secretion. Thus, in the context of regulating prolactin secretion, dopamine is occasionally called prolactin-inhibiting factor (PIF), prolactin-inhibiting hormone (PIH), or prolactostatin. Prolactin also seems to inhibit dopamine release, such as after orgasm, and is chiefly responsible for the refractory period.

Motivation and pleasure Edit

Reinforcement Edit

Dopamine is commonly associated with the pleasure system of the brain, providing feelings of enjoyment and reinforcement to motivate a person proactively to perform certain activities. Dopamine is released (particularly in areas such as the nucleus accumbens and ventral tegmental area) by naturally rewarding experiences such as food, sex,[5][6] some drugs, and neutral stimuli that become associated with them. This theory is often discussed in terms of drugs such as cocaine, nicotine,and amphetamines, which seem to directly or indirectly lead to the increase of dopamine in these areas, and in relation to neurobiological theories of chemical addiction, arguing that these dopamine pathways are pathologically altered in addicted persons.

Reuptake inhibition, expulsion Edit

However, cocaine and amphetamine influence separate mechanisms of action. Cocaine is a dopamine transporter blocker that competitively inhibits dopamine uptake to increase the lifetime of dopamine and augments an overabundance of dopamine (an increase of up to 150 percent) within the parameters of the dopamine neurotransmitters.

Like cocaine, amphetamines increase the concentration of dopamine in the synaptic gap, but by a different mechanism. Amphetamines are similar in structure to dopamine, and so can enter the terminal button of the presynaptic neuron via its dopamine transporters as well as by diffusing through the neural membrane directly. When entering inside the presynaptic neuron, amphetamines force the dopamine molecules out of their storage vesicles and expel them into the synaptic gap by making the dopamine transporters work in reverse.

Incentive salience Edit

Dopamine's role in experiencing pleasure has been questioned by several researchers. It has been argued that dopamine is more associated with anticipatory desire and motivation (commonly referred to as "wanting") as opposed to actual consummatory pleasure (commonly referred to as "liking"). Dopamine is not released when unpleasant or aversive stimuli are encountered, and so motivates towards the pleasure of avoiding or removing the unpleasant stimuli.

Dopamine, learning, and reward-seeking behavior Edit

Dopaminergic neurons of the midbrain are the main source of dopamine in the brain.[7] Dopamine has been shown to be involved in the control of movements, the signaling of error in prediction of reward, motivation, and cognition. Cerebral dopamine depletion is the hallmark of Parkinson´s disease.[7] Other pathological states have also been associated with dopamine dysfunction, such as schizophrenia, autism, and attention deficit hyperactivity disorder in children, as well as drug abuse. Dopamine is closely associated with reward-seeking behaviors, such as approach, consumption, and addiction.[7] Recent researches suggest that the firing of dopaminergic neurons is a motivational substance as a consequence of reward-anticipation. This hypothesis is based on the evidence that, when a reward is greater than expected, the firing of certain dopaminergic neurons increases, which consequently increases desire or motivation towards the reward.[7]

Animal studies Edit

Clues to dopamine's role in motivation, desire, and pleasure have come from studies performed on animals. In one such study, rats were depleted of dopamine by up to 99 percent in the nucleus accumbens and neostriatum using 6-hydroxydopamine.[7] With this large reduction in dopamine, the rats would no longer eat by their own volition. The researchers then force-fed the rats food and noted whether they had the proper facial expressions indicating whether they liked or disliked it. The researchers of this study concluded that the reduction in dopamine did not reduce the rat's consummatory pleasure, only the desire to actually eat. In another study, mutant hyperdopaminergic (increased dopamine) mice show higher "wanting" but not "liking" of sweet rewards.[8]

Dopamine reducing drugs in humans Edit

In humans, however, drugs that reduce dopamine activity (neuroleptics, e.g., some antipsychotics) have been shown to reduce motivation, as well as cause anhedonia (the inability to experience pleasure).[9] Selective D2/D3 agonists pramipexole and ropinirole as used in Restless legs syndrome have limited anti-anhedonic properties as measured by the Snaith-Hamilton Pleasure Scale.[10] (The Snaith-Hamilton-Pleasure-Scale (SHAPS), introduced in English in 1995, assesses self-reported anhedonia in psychiatric patients.).These drugs have side effects like "hyper sexuality" and "compulsive gambling" which are pleasure determined effects of dopamine.[How to reference and link to summary or text]

Main article: Dopamine antagonists

Opioid and cannabinoid transmission Edit

Opioid and cannabinoid transmission instead of dopamine may modulate consummatory pleasure and food palatability (liking).[11] This could explain why animals' "liking" of food is independent of brain dopamine concentration. Other consummatory pleasures, however, may be more associated with dopamine. One study found that both anticipatory and consummatory measures of sexual behavior (male rats) were disrupted by DA receptor antagonists.[12] Libido can be increased by drugs that affect dopamine, but not by drugs that affect opioid peptides or other neurotransmitters.

Sociability Edit

Sociability is also closely tied to dopamine neurotransmission. Low D2 receptor-binding is found in people with social anxiety. Traits common to negative schizophrenia (social withdrawal, apathy, anhedonia) are thought to be related to a hypodopaminergic state in certain areas of the brain. In instances of bipolar disorder, manic subjects can become hypersocial, as well as hypersexual. This is also credited to an increase in dopamine, because mania can be reduced by dopamine-blocking anti-psychotics.

Salience Edit

Dopamine may also have a role in the salience ('noticeableness') of perceived objects and events, with potentially important stimuli such as: 1) rewarding things or 2) dangerous or threatening things seeming more noticeable or important.[13] This hypothesis argues that dopamine assists decision-making by influencing the priority, or level of desire, of such stimuli to the person concerned.

Behavior disorders Edit

Pharmacological blockade of brain dopamine receptors increases rather than decreases drug-taking behaviour. Since blocking dopamine decreases desire, the increase in drug-taking behaviour may be seen as not a chemical desire but as a deeply psychological desire to just 'feel something'.

Deficits in dopamine levels are implicated in attention-deficit hyperactivity disorder (ADHD), and stimulant medications used to successfully treat the disorder increase dopamine neurotransmitter levels, leading to decreased symptoms.

Latent inhibition and creative drive Edit

Dopamine in the mesolimbic pathway increases general arousal and goal directed behaviors and decreases latent inhibition; all three effects increase the creative drive of idea generation. This has led to a three-factor model of creativity involving the frontal lobes, the temporal lobes, and mesolimbic dopamine.[14]

Links to psychosis Edit

Main article: Dopamine hypothesis of psychosis

Abnormally high dopamine action has also been strongly linked to psychosis and schizophrenia,[15] Dopamine neurons in the mesolimbic pathway are particularly associated with these conditions. Evidence comes partly from the discovery of a class of drugs called the phenothiazines (which block D2 dopamine receptors) that can reduce psychotic symptoms, and partly from the finding that drugs such as amphetamine and cocaine (which are known to greatly increase dopamine levels) can cause psychosis.[16] Because of this, most modern antipsychotic medications, for example, Risperidone, are designed to block dopamine function to varying degrees.

Therapeutic use Edit

Main article: L-DOPA

Levodopa is a dopamine precursor used in various forms to treat Parkinson's disease. It is typically co-administered with an inhibitor of peripheral decarboxylation (DDC, dopa decarboxylase), such as carbidopa or benserazide. Inhibitors of alternative metabolic route for dopamine by catechol-O-methyl transferase are also used. These include entacapone and tolcapone.

Dopamine is also used as an inotropic drug in patients with shock to increase cardiac output and blood pressure.

See also Edit

  • Serotonin-dopamine reuptake inhibitor
  • References Edit

    1. Benes, F.M. Carlsson and the discovery of dopamine. Trends in Pharmacological Sciences, Volume 22, Issue 1, 1 January 2001, Pages 46-47.
    2. Fahn, Stanley, "The History of Levodopa as it Pertains to Parkinson’s Disease," Movement Disorder Society’s 10th International Congress of Parkinson's Disease and Movement Disorders on November 1, 2006, in Kyoto, Japan.
    3. Barron AB, Maleszka R, Vander Meer RK, Robinson GE (2007). Octopamine modulates honey bee dance behavior. Proc. Natl. Acad. Sci. U.S.A. 104 (5): 1703-7.
    4. Schultz, Cambridge university, UK
    5. Giuliano, F., Allard J. (2001). Dopamine and male sexual function. Eur Urol 40: 601-608.
    6. Giuliano, F., Allard J. (2001). Dopamine and sexual function. Int J Impot Res 13 (Suppl 3): S18-S28.
    7. 7.0 7.1 7.2 7.3 7.4 Arias-Carrión O, Pöppel E (2007). Dopamine, learning and reward-seeking behavior. Act Neurobiol Exp 67 (4): 481-488. PMID.
    8. Peciña S, Cagniard B, Berridge K, Aldridge J, Zhuang X (2003). Hyperdopaminergic mutant mice have higher "wanting" but not "liking" for sweet rewards.. J Neurosci 23 (28): 9395-402. PMID 14561867.
    9. Lambert M, Schimmelmann B, Karow A, Naber D (2003). Subjective well-being and initial dysphoric reaction under antipsychotic drugs - concepts, measurement and clinical relevance.. Pharmacopsychiatry 36 (Suppl 3): S181-90.
    10. Lemke M, Brecht H, Koester J, Kraus P, Reichmann H (2005). Anhedonia, depression, and motor functioning in Parkinson's disease during treatment with pramipexole.. J Neuropsychiatry Clin Neurosci 17 (2): 214-20.
    11. Peciña S, Berridge K (2005). Hedonic hot spot in nucleus accumbens shell: where do mu-opioids cause increased hedonic impact of sweetness?. J Neurosci 25 (50): 11777-86. PMID 16354936.
    12. Pfaus J, Phillips A (1991). Role of dopamine in anticipatory and consummatory aspects of sexual behavior in the male rat.. Behav Neurosci 105 (5): 727-43. PMID 1840012.
    13. Schultz W (2002). Getting formal with dopamine and reward. Neuron 36 (2): 241-263. PMID 12383780.
    14. Flaherty, A.W, (2005). Frontotemporal and dopaminergic control of idea generation and creative drive. Journal of Comparative Neurology 493 (1): 147-153.
    15. Disruption of gene interaction linked to schizophrenia. St. Jude Children's Research Hospital. URL accessed on 2006-07-06.
    16. Lieberman, J.A., JM Kane, J. Alvir (1997). Provocative tests with psychostimulant drugs in schizophrenia.. Psychopharmacology (Berl). 91 (4): 415-433. PMID 2884687.


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