The molecular and cellular mechanisms of depression: a focus on reward circuitry

被引:133
|
作者
Fox, Megan E. [1 ]
Lobo, Mary Kay [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Anat & Neurobiol, Baltimore, MD 21201 USA
关键词
SOCIAL DEFEAT STRESS; DOPAMINE NEURON ACTIVITY; PULMONARY ARTERIAL-HYPERTENSION; MOUSE NUCLEUS-ACCUMBENS; RHO-KINASE INHIBITOR; CHRONIC MILD STRESS; DELTA-FOSB; CHOLINERGIC INTERNEURONS; NEUROTROPHIC FACTOR; STRIATAL DOPAMINE;
D O I
10.1038/s41380-019-0415-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Depression is a complex disorder that takes an enormous toll on individual health. As affected individuals display a wide variation in their clinical symptoms, the precise neural mechanisms underlying the development of depression remain elusive. Although it is impossible to phenocopy every symptom of human depression in rodents, the preclinical field has had great success in modeling some of the core affective and neurovegetative depressive symptoms, including social withdrawal, anhedonia, and weight loss. Adaptations in select cell populations may underlie these individual depressive symptoms and new tools have expanded our ability to monitor and manipulate specific cell types. This review outlines some of the most recent preclinical discoveries on the molecular and neurophysiological mechanisms in reward circuitry that underlie the expression of behavioral constructs relevant to depressive symptoms.
引用
收藏
页码:1798 / 1815
页数:18
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