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Cannabinoid CB1 receptors in the amygdalar cholecystokinin glutamatergic afferents to nucleus accumbens modulate depressive-like behavior.

Abstract：

:Major depressive disorder is a devastating psychiatric disease that afflicts up to 17% of the world's population. Postmortem brain analyses and imaging studies of patients with depression have implicated basal lateral amygdala (BLA) dysfunction in the pathophysiology of depression. However, the circuit and molecular mechanisms through which BLA neurons modulate depressive behavior are largely uncharacterized. Here, in mice, we identified that BLA cholecystokinin (CCK) glutamatergic neurons mediated negative reinforcement via D2 medium spiny neurons (MSNs) in the nucleus accumbens (NAc) and that chronic social defeat selectively potentiated excitatory transmission of the CCKBLA-D2NAc circuit in susceptible mice via reduction of presynaptic cannabinoid type-1 receptor (CB1R). Knockdown of CB1R in the CCKBLA-D2NAc circuit elevated synaptic activity and promoted stress susceptibility. Notably, selective inhibition of the CCKBLA-D2NAc circuit or administration of synthetic cannabinoids in the NAc was sufficient to produce antidepressant-like effects. Overall, our studies reveal the circuit and molecular mechanisms of depression.

journal_name

Nat Med

journal_title

Nature medicine

authors

Shen CJ,Zheng D,Li KX,Yang JM,Pan HQ,Yu XD,Fu JY,Zhu Y,Sun QX,Tang MY,Zhang Y,Sun P,Xie Y,Duan S,Hu H,Li XM

doi

10.1038/s41591-018-0299-9

subject

Has Abstract

pub_date

2019-02-01 00:00:00

pages

337-349

issue

2

eissn

1078-8956

issn

1546-170X

pii

10.1038/s41591-018-0299-9

journal_volume

25

pub_type

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