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Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
Located deep in the brain's medial temporal lobe, the almond-shaped amygdala (in Latin, corpus amygdaloideum) is believed to play a key role in the emotions. It forms part of the limbic system. In humans and other animals, this subcortical brain structure is linked to both fear responses and pleasure. Its size is positively correlated with aggressive behavior across species. In humans it is the most sexually dimorphic brain structure, and shrinks by more than 30% in males upon castration. Conditions such as anxiety, autism, depression, post-traumatic stress disorder, and phobias are suspected of being linked to abnormal functioning of the amygdala owing to damage, developmental problems, or neurotransmitter imbalance.
Anatomical subdivisions
The amygdala is actually several separately functioning nuclei that anatomists group together by the proximity of the nuclei to one another. Key among these nuclei are the basolateral complex, the centromedial nucleus, and the cortical nucleus.
Connections
The basolateral complex receives input from the sensory systems and is necessary for fear conditioning in rats. The centromedial nucleus is the main output for the basolateral complex and is involved in emotional arousal in rats and cats. The amygdala sends outputs to the hypothalamus for activation of the sympathetic nervous system, the reticular nucleus for increased reflexes, the nuclei of the trigeminal nerve and facial nerve for facial expressions of fear, and the ventral tegmental area, locus ceruleus, and laterodorsal tegmental nucleus for activation of dopamine, norepinephrine and epinephrine. The cortical nucleus is involved in olfaction and pheromone processing. It receives input from the olfactory bulb and olfactory cortex.
Memory modulation and drug addiction
The amygdala plays a key role in the modulation of memory consolidation. Following any learning event, the long-term memory for the event is not instantaneously formed. Rather, information regarding the event is slowly put into long-term storage over time, a process referred to as "memory consolidation", until it reaches a relatively permanent state. During the consolidation period, the memory can be modulated. In particular, it appears that emotional arousal following the learning event influences the strength of the subsequent memory for that event. Greater emotional arousal following a learning event enhances a person's retention of that event. Experiments have shown that administration of stress hormones to a person immediately after the person learns something enhances that person's retention when they are tested two weeks later.
The amygdala, especially the basolateral amygdala, plays a key role in mediating the effects of emotional arousal on the strength of the memory for the event, as shown by many laboratories including that of James McGaugh. These laboratories have trained animals on a variety of learning tasks and found that drugs injected into the amygdala after training affect the animals' subsequent retention of the task. These tasks include basic Pavlovian tasks such as inhibitory avoidance (where a rat learns to associate a mild footshock with a particular compartment of an apparatus) and more complex tasks such as spatial or cued water maze (where a rat learns to swim to a platform to escape the water). If a drug that activates the amygdala is injected into the amygdala, the animal has better memory for the training in the task. If a drug that inactivates the amygdala is injected into it, the animal has impaired memory for the task.
Despite the importance of the amygdala in modulating memory consolidation, however, learning can occur without it, though such learning appears to be impaired.
Evidence from work with humans indicates that the amygdala plays a similar role. Amygdala activity at the time of encoding information correlates with retention for that information. However, this correlation depends on the relative "emotionalness" of the information. More emotionally arousing information increases amygdala activity and that activity correlates with retention.
Experiments with rats also suggest that the amygdala is involved in learning about various cues with the consumption of drugs of abuse. It is well known that one of the major problems in drug addiction is that drug-associated cues induce significant craving in individuals, even if the individuals have not taken the drugs in a long time. The amygdala appears to play a key role in the initial learning of the association between the cues and the drugs. In addition, inactivation of the amygdala prevents the ability of cues to induce reinstatement in rats in a drug self-administration paradigm.
See also
- Removal of the amygdala[1] from monkeys results in Kluver-Bucy syndrome.
- Stathmin gene and Amygdala: Recent research works by Dr. Gleb Shumyatsky and Prof. Eric Kandel have led to the identification of the Stathmin gene. This gene is highly enriched in the Amygdala and is believed to be involved in controlling both innate and learned fear in mice. They "knocked out" the stathmin gene in the amygdala using gene knockout technology and found that mice that lacked stathmin gene lacked any kind of fear. For instance, such mice did not freeze on sighting a cat.
References
- Kandel ER, Schwartz JH, Jessell TM. Principles of Neural Science, 4th ed. McGraw-Hill, New York (2000). ISBN 0838577016
External links:
- BrainMaps at UCDavis amygdala
- Amygdala, Panic and Post Traumatic Stress
- BrainInfo at the University of Washington hier-219
Human brain: Limbic system | |
Amygdala - Cingulate gyrus - Fornicate gyrus - Hippocampus - Hypothalamus - Mammillary body - Nucleus accumbens - Orbitofrontal cortex - Parahippocampal gyrus |
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