The cation channel mechanisms of subthreshold inward depolarizing currents in the VTA dopaminergic neurons and their roles in the chronic-stress-induced depression-like behavior

Author:

Wang Jing12,Su Min13,Zhang Dongmei14,Zhang Ludi1,Niu Chenxu1,Li Chaoyi1,You Shuangzhu1,Sang Yuqi156,Zhang Yongxue17,Du Xiaona1,Zhang Hailin18

Affiliation:

1. Department of Pharmacology; The Key Laboratory of Neural and Vascular Biology, Ministry of Education; The Key Laboratory of New Drug Pharmacology and Toxicology, Hebei Medical University

2. Department of Pharmacochemistry, Hebei University of Chinese Medicine

3. Yiling Pharmaceutical Company

4. Department of Clinical Pharmacy, Xintai Ninth Hoapital

5. College of Chemical Engineering, Shijiazhuang University

6. Shijiazhuang Key Laboratory of Targeted Drugs Research and Efficacy Evaluation

7. Department of Pharmacy, Handan First Hospital

8. Department of Psychiatry, The First Hospital of Hebei Medical University, Mental Health Institute of Hebei Medical University

Abstract

The slow-intrinsic-pacemaker dopaminergic (DA) neurons originating in the ventral tegmental area (VTA) are implicated in various mood- and emotion-related disorders, such as anxiety, fear, stress and depression. Abnormal activity of projection-specific VTA DA neurons is the key factor in the development of these disorders. Here, we describe the crucial role for the NALCN and TRPC6, non-selective cation channels in mediating the subthreshold inward depolarizing current and driving the firing of action potentials of VTA DA neurons in physiological condition. Furthermore, we demonstrate that down-regulation of TRPC6 protein expression in the VTA DA neurons likely contributes to the reduced activity of projection-specific VTA DA neuron in chronic mild unpredictable stress (CMUS) depressive mice. In consistent with these, selective knockdown of TRPC6 channels in the VTA DA neurons conferred mice with depression-like behavior. This current study suggests down-regulation of TRPC6 expression/function is involved in reduced VTA DA neuron firing and chronic stress-induced depression-like behavior of mice.

Publisher

eLife Sciences Publications, Ltd

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