Biology of
depression
Scientific studies have found that different brain areas show altered activity in people with major
depressive disorder (MDD), and this has encouraged advocates of various theories that seek to
identify a biochemical origin of the disease, as opposed to theories that emphasize
psychological or situational causes. Factors spanning these causative groups include nutritional
deficiencies in magnesium, vitamin D, and tryptophan with situational origin but biological
impact. Several theories concerning the biologically based cause of depression have been
suggested over the years, including theories revolving around monoamine neurotransmitters,
neuroplasticity, neurogenesis, inflammation and the circadian rhythm. Physical illnesses,
including hypothyroidism and mitochondrial disease, can also trigger depressive symptoms.[1][2]
Neural circuits implicated in depression include those involved in the generation and regulation
of emotion, as well as in reward. Abnormalities are commonly found in the lateral prefrontal
cortex whose putative function is generally considered to involve regulation of emotion. Regions
involved in the generation of emotion and reward such as the amygdala, anterior cingulate
cortex (ACC), orbitofrontal cortex (OFC), and striatum are frequently implicated as well. These
regions are innervated by a monoaminergic nuclei, and tentative evidence suggests a potential
role for abnormal monoaminergic activity.[3][4]
Genetic factors
Circadian rhythm
Monoamines
Emotional processing and neural circuits
Neuroanatomy
Animal Models
Altered neuroplasticity
Inflammation
Oxidative stress
Large-scale brain network theory
See also
References
Further reading
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