Amygdala: For Other Uses, See Amygdala (Disambiguation)
Amygdala: For Other Uses, See Amygdala (Disambiguation)
Amygdala: For Other Uses, See Amygdala (Disambiguation)
Amygdala
Details
Identifiers
MeSH D000679
NeuroNames 237
NeuroLex ID birnlex_1241
TA A14.1.09.402
FMA 61841
[edit on Wikidata]
Human brain in the coronal orientation. Amygdalae are shown in dark red.
Contents
1Structure
o 1.1Hemispheric specializations
2Development
o 2.1Sex distinction
3Function
o 3.1Connections
o 3.2Emotional learning
o 3.3Reward
o 3.4Memory modulation
o 4.1Sexual orientation
o 4.2Social interaction
o 4.3Aggression
o 4.4Fear
o 4.6Anxiety
o 4.8Bipolar disorder
o 4.9Political orientation
5See also
6Further reading
7References
8External links
Structure[edit]
The regions described as amygdala nuclei encompass several structures with distinct
connectional and functional characteristics in humans and other animals. [4] Among these nuclei
are the basolateral complex, the cortical nucleus, the medial nucleus, the central nucleus, and
the intercalated cell clusters. The basolateral complex can be further subdivided into the lateral,
the basal, and the accessory basal nuclei.[3][5][6]
Anatomically, the amygdala,[7] and more particularly its central and medial nuclei,[8] have
sometimes been classified as a part of the basal ganglia.
Hemispheric specializations[edit]
There are functional differences between the right and left amygdala. In one study, electrical
stimulations of the right amygdala induced negative emotions, especially fear and sadness. In
contrast, stimulation of the left amygdala was able to induce either pleasant (happiness) or
unpleasant (fear, anxiety, sadness) emotions.[9] Other evidence suggests that the left amygdala
plays a role in the brain's reward system.[10]
Each side holds a specific function in how we perceive and process emotion. The right and left
portions of the amygdala have independent memory systems, but work together to store,
encode, and interpret emotion.
The right hemisphere is associated with negative emotion. It plays a role in the expression of fear
and in the processing of fear-inducing stimuli. Fear conditioning, which occurs when a neutral
stimulus acquires aversive properties, occurs within the right hemisphere. When an individual is
presented with a conditioned, aversive stimulus, it is processed within the right amygdala,
producing an unpleasant or fearful response. This emotional response conditions the individual
to avoid fear-inducing stimuli.
The right hemisphere is also linked to declarative memory, which consists of facts and
information from previously experienced events and must be consciously recalled. It also plays a
significant role in the retention of episodic memory. Episodic memory consists of the
autobiographical aspects of memory, permitting you to recall your personal emotional and
sensory experience of an event. This type of memory does not require conscious recall. The right
amygdala plays a role in the association of time and places with emotional properties. [11]
Development[edit]
There is considerable growth within the first few years of structural development in both male and
female amygdalae.[12] Within this early period, female limbic structures grow at a more rapid pace
than the male ones. Amongst female subjects, the amygdala reaches its full growth potential
approximately 1.5 years before the peak of male development. The structural development of the
male amygdala occurs over a longer period than in women. Despite the early development of
female amygdalae, they reach their growth potential sooner than males, whose amygdalae
continue to develop. The larger relative size of the male amygdala may be attributed to this
extended developmental period.
In addition to longer periods of development, other neurological and hormonal factors may
contribute to sex-specific developmental differences. The amygdala is rich in androgen receptors
– nuclear receptors that bind to testosterone. Androgen receptors play a role in the DNA binding
that regulates gene expression. Though testosterone is present within the female hormonal
systems, women have lower levels of testosterone than men. The abundance of testosterone in
the male hormonal system may contribute to development. In addition, the grey matter volume
on the amygdala is predicted by testosterone levels, which may also contribute to the increased
mass of the male amygdala.
In addition to sex differences, there are observable developmental differences between the right
and left amygdala in both males and females. The left amygdala reaches its developmental peak
approximately 1.5–2 years prior to the right amygdala. Despite the early growth of the left
amygdala, the right increases in volume for a longer period of time. The right amygdala is
associated with response to fearful stimuli as well as face recognition. It is inferred that the early
development of the left amygdala functions to provide infants the ability to detect danger. [12]In
childhood, the amygdala is found to react differently to same-sex versus opposite-sex individuals.
This reactivity decreases until a person enters adolescence, where it increases dramatically at
puberty.[13]
Sex distinction[edit]
See also: Neuroscience of sex differences
The amygdala is one of the best-understood brain regions with regard to differences between the
sexes. The amygdala is larger in males than females in children ages 7–11, [14] in adult humans,
[15]
and in adult rats.[16]
In addition to size, other functional and structural differences between male and female
amygdalae have been observed. Subjects' amygdala activation was observed when watching a
horror film and subliminal stimuli. The results of the study showed a different lateralization of the
amygdala in men and women. Enhanced memory for the film was related to enhanced activity of
the left, but not the right, amygdala in women, whereas it was related to enhanced activity of the
right, but not the left, amygdala in men. [17] One study found evidence that on average, women
tend to retain stronger memories for emotional events than men. [18]
The right amygdala is also linked with taking action as well as being linked to negative emotions,
[19]
which may help explain why males tend to respond to emotionally stressful stimuli physically.
The left amygdala allows for the recall of details, but it also results in more thought rather than
action in response to emotionally stressful stimuli, which may explain the absence of physical
response in women.
Function[edit]
Connections[edit]
The amygdala sends projections to the hypothalamus, the dorsomedial thalamus, the thalamic
reticular nucleus, the nuclei of the trigeminal nerve and the facial nerve, the ventral tegmental
area, the locus coeruleus, and the laterodorsal tegmental nucleus.[5] The basolateral amygdala
projects to the nucleus accumbens, including the medial shell. [20][21]
Coronal section of brain through intermediate mass of third ventricle. Amygdala is shown in purple.
The medial nucleus is involved in the sense of smell and pheromone-processing. It receives
input from the olfactory bulb and olfactory cortex.[22] The lateral amygdalae, which send impulses
to the rest of the basolateral complexes and to the centromedial nuclei, receive input from the
sensory systems. The centromedial nuclei are the main outputs for the basolateral complexes,
and are involved in emotional arousal in rats and cats.[5][6][23]
Emotional learning[edit]
Main article: Emotion and memory
In complex vertebrates, including humans, the amygdalae perform primary roles in the formation
and storage of memories associated with emotional events. Research indicates that, during fear
conditioning, sensory stimuli reach the basolateral complexes of the amygdalae, particularly the
lateral nuclei, where they form associations with memories of the stimuli. The association
between stimuli and the aversive events they predict may be mediated by long-term potentiation,
[24][25]
a sustained enhancement of signaling between affected neurons. [26] There have been studies
that show that damage to the amygdala can interfere with memory that is strengthened by
emotion. One study examined a patient with bilateral degeneration of the amygdala. He was told
a violent story accompanied by matching pictures and was observed based on how much he
could recall from the story. The patient had less recollection of the story than patients with
functional amygdala, showing that the amygdala has a strong connection with emotional
learning.[27]
Emotional memories are thought to be stored in synapses throughout the brain. Fear memories,
for example, are considered to be stored in the neuronal connections from the lateral nuclei to
the central nucleus of the amygdalae and the bed nuclei of the stria terminalis (part of
the extended amygdala). Of course, these connections are not the sole site of fear memories
given that the nuclei of the amygdala receive and send information to other brain regions that are
important for memory such as the hippocampus. Some sensory neurons project their axon
terminals to the central nucleus.[28] The central nuclei are involved in the genesis of many fear
responses such as defensive behavior (freezing or escape responses), autonomic nervous
system responses (changes in blood pressure and heart rate/tachycardia), neuroendocrine
responses (stress-hormone release), etc. Damage to the amygdalae impairs both the acquisition
and expression of Pavlovian fear conditioning, a form of classical conditioning of emotional
responses.[26]
The amygdalae are also involved in appetitive (positive) conditioning. It seems that distinct
neurons respond to positive and negative stimuli, but there is no clustering of these distinct
neurons into clear anatomical nuclei.[29][30] However, lesions of the central nucleus in the amygdala
have been shown to reduce appetitive learning in rats. Lesions of the basolateral regions do not
exhibit the same effect.[31] Research like this indicates that different nuclei within the amygdala
have different functions in appetitive conditioning. [32][33]Nevertheless, researchers found an
example of appetitive emotional learning showing an important role for the basolateral amygdala:
The naïve female mice are innately attracted to non-volatile pheromones contained in male-
soiled bedding, but not by the male-derived volatiles, become attractive if associated with non-
volatile attractive pheromones, which act as unconditioned stimulus in a case of Pavlovian
associative learning.[34] In the vomeronasal, olfactory and emotional systems, Fos protein show
that non-volatile pheromones stimulate the vomeronasal system, whereas air-borne volatiles
activate only the olfactory system. Thus, the acquired preference for male-derived volatiles
reveals an olfactory-vomeronasal associative learning. Moreover, the reward system is
differentially activated by the primary pheromones and secondarily attractive odorants. Exploring
the primary attractive pheromone activates the basolateral amygdala and the shell of nucleus
accumbens but neither the ventral tegmental area nor the orbitofrontal cortex. In contrast,
exploring the secondarily attractive male-derived odorants involves activation of a circuit that
includes the basolateral amygdala, prefrontal cortex and ventral tegmental area. Therefore, the
basolateral amygdala stands out as the key center for vomeronasal-olfactory associative
learning.[35]
Reward[edit]
Glutaminergic neurons in the basolateral amygdala send projections to the nucleus
accumbens(NAc) shell and core. Activation of these projections drive motivational salience. The
ability of these projections to drive incentive salience is dependent upon dopamine receptor D1.[20]
[21]
Memory modulation[edit]
The amygdala is also involved in the modulation of memory consolidation. Following any learning
event, the long-term memory for the event is not formed instantaneously. Rather, information
regarding the event is slowly assimilated into long-term (potentially lifelong) storage over time,
possibly via long-term potentiation. Recent studies suggest that the amygdala regulates memory
consolidation in other brain regions. Also, fear conditioning, a type of memory that is impaired
following amygdala damage, is mediated in part by long-term potentiation. [24][25]
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 mice
immediately after they learn something enhances their retention when they are tested two days
later.[36]
The amygdala, especially the basolateral nuclei, are involved 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 classical conditioning 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
amygdalae is injected into the amygdalae, the animals had better memory for the training in the
task.[37] If a drug that inactivates the amygdalae is injected, the animals had impaired memory for
the task.
Buddhist monks who do compassion meditation have been shown to modulate their amygdala,
along with their temporoparietal junction and insula, during their practice.[38] In an fMRI study,
more intensive insula activity was found in expert meditators than in novices. [39]Increased activity
in the amygdala following compassion-oriented meditation may contribute to social
connectedness.[40]
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 amygdalar activity, and that activity correlates
with retention. Amygdala neurons show various types of oscillation during emotional arousal,
such as theta activity. These synchronized neuronal events could promote synaptic
plasticity (which is involved in memory retention) by increasing interactions between neocortical
storage sites and temporal lobe structures involved in declarative memory.[41]
Research using Rorschach test blot 03 finds that the number of unique responses to this random
figure links to larger sized amygdalae. The researchers note, "Since previous reports have
indicated that unique responses were observed at higher frequency in the artistic population than
in the nonartistic normal population, this positive correlation suggests that amygdalar
enlargement in the normal population might be related to creative mental activity." [42]
See also[edit]
Amygdala hijack
BELBIC
Triune brain
Further reading[edit]
Amygdala Joseph E. LeDoux, Scholarpedia, 3(4):2698. doi:10.4249/scholarpedia.2698
Fear
Anger
Happiness
Love
Bottom line
Overview
The brain is a very complex organ. It controls and coordinates everything
from the movement of your fingers to your heart rate. The brain also plays
a crucial role in how you control and process your emotions.
Experts still have a lot of questions about the brain’s role in a range of
emotions, but they’ve pinpointed the origins of some common ones,
including fear, anger, happiness, and love.
Read on to learn more about what part of the brain controls emotions.
Scientists haven’t reached an agreement about the full list of structures that
make up the limbic system, but the following structures are generally
accepted as part of the group:
Limbic cortex. This part contains two structures, the cingulate gyrus
and the parahippocampal gyrus. Together, they impact mood,
motivation, and judgement.
What part of the brain controls
fear?
From a biological standpoint, fear is a very important emotion. It helps you
respond appropriately to threatening situations that could harm you.
As these hormones enter the bloodstream, you might notice some physical
changes, such as an increase in:
heart rate
breathing rate
blood sugar
perspiration
Anger starts with the amygdala stimulating the hypothalamus, much like in
the fear response. In addition, parts of the prefrontal cortex may also play a
role in anger. People with damage to this area often have trouble
controlling their emotions, especially anger and aggression.
Parts of the prefrontal cortex of the brain may also contribute to the
regulation of an anger response. People with damage to this area of the
brain sometimes have difficulty controlling their emotions, particularly
anger and aggression.
A 2015 study found that people with larger gray matter volume in their
right precuneus reported being happier. Experts think the precuneus
processes certain information and converts it into feelings of happiness. For
example, imagine you’ve spent a wonderful night out with someone you
care about. Going forward, when you recall this experience and others like
it, you may experience a feeling of happiness.
Dopamine is associated with your body’s reward system. This helps make
love a desirable feeling.
As technology evolves and scientists get a better glimpse into the human
mind, we’ll likely learn more about the origins of more complex emotions.