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Published on: February 12, 2020
Ventral tegmental area dopaminergic neurons mediate electroacupuncture relief of stress-induced depression in mice
Liting Yang1, Xuanjie Yu2, Qianhui Yang1
1School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning, China; School of Basic Medicine Sciences, Xianning Medical College, Hubei University of Science and Technology, Xianning, China.
Aims:
Depression is a prevalent mood disorder characterized by persistent low mood and cognitive deficits that severely impaired quality of life. Despite intensive research, its precise pathogenesis remained elusive, and a considerable proportion of patients were refractory to existing therapies. Recent work has highlighted ventral tegmental area (VTA) dopaminergic (DAergic) neurons in the pathophysiology of depression because of their central role in reward processing and motivation. In this study, we provided direct evidence that VTADA neurons were implicated in the alterations evoked by 21-day chronic restraint stress (CRS) in mice.
Materials And Methods:
Employing in vivo fiber photometry, chemogenetics, behavioral tests, and immunofluorescence, we investigated the effect of VTADA neurons of regulation on depressive behavior of the CRS mice.
Key Findings:
The activity of VTADA neurons was markedly decreased in CRS exposed animals. Chemogenetic activation of these neurons alleviated depression like symptoms, whereas their inhibition induced depression like phenotypes in the absence of stress. Electroacupuncture (EA) has garnered substantial clinical attention for mood disorders because of its established safety, minimal adverse effects, and robust therapeutic efficacy. Here, EA at specific acupoints reversed CRS induced behavioral deficits and restored VTADA neuron activity. However, chemogenetic inhibition of VTADA neurons during EA abolished its antidepressant effects.
Significance:
Collectively, our findings provided mechanistic insight into the contribution of VTADA neurons to CRS induced depression.
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