Jiang Ning, Huang Hong, Wang Haixia, Lv Jingwei, Zeng Guirong, Wang Qiong, Bao Yu, Chen Ying, Liu Xin-Min
Research Center for Pharmacology and Toxicology, Institute of Medicinal Plant Development (IMPLAD), Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Affiliated TCM Hospital/School of Pharmacy/Sino-Portugal TCM International Cooperation Center, Southwest Medical University, Luzhou, China.
Phytother Res. 2021 May;35(5):2711-2726. doi: 10.1002/ptr.7017. Epub 2021 Jan 20.
The Shen Yuan prescription (SY) comprises Panax ginseng (GT) and Polygala tenuifolia (YT), elicited superior antidepressant activity compared with that of GT or YT alone. The aim of this paper is to elucidate the effects of SY treatment on chronic social defeat stress (CSDS)-induced depression-like symptoms and the related mechanism. Our results indicated that SY treatment reverses the depressive-like behaviors induced by CSDS as measured by the social interaction test, sucrose preference test, forced swim test, and tail suspension test. SY decreased the serum levels of CORT and increased hippocampal neurotransmitters (5-HT, DA, and NE) in CSDS mice. Meanwhile, SY upregulated the brain-derived neurotrophic factor (BDNF) signaling pathway and reversed the decreased hippocampal neurogenesis caused by CSDS. In addition, we found that the TrkB antagonist K252a fully blocked the SY effects on behavioral improvement and eliminated the promoting effects of SY on hippocampal neurogenesis and BDNF-TrkB signaling (including the downstream ERK and Akt pathways) activation, thus further demonstrating that BDNF-TrkB signaling was necessary for the SY effects. In conclusion, our study showed that SY acted as an antidepressant in mice exhibiting CSDS-induced depression-like symptoms, and its effect was facilitated by promoting hippocampal neurogenesis and BDNF signaling pathway activation.
神源方(SY)由人参(GT)和远志(YT)组成,与单独使用GT或YT相比,具有更强的抗抑郁活性。本文旨在阐明SY治疗对慢性社会挫败应激(CSDS)诱导的抑郁样症状的影响及其相关机制。我们的结果表明,通过社会互动测试、蔗糖偏好测试、强迫游泳测试和悬尾测试测量,SY治疗可逆转CSDS诱导的抑郁样行为。SY降低了CSDS小鼠的血清皮质酮(CORT)水平,并增加了海马神经递质(5-羟色胺、多巴胺和去甲肾上腺素)。同时,SY上调了脑源性神经营养因子(BDNF)信号通路,并逆转了CSDS导致的海马神经发生减少。此外,我们发现TrkB拮抗剂K252a完全阻断了SY对行为改善的作用,并消除了SY对海马神经发生和BDNF-TrkB信号(包括下游的ERK和Akt通路)激活的促进作用,从而进一步证明BDNF-TrkB信号对SY的作用是必要的。总之,我们的研究表明,SY对表现出CSDS诱导的抑郁样症状的小鼠具有抗抑郁作用,其作用是通过促进海马神经发生和BDNF信号通路激活来实现的。