Saikosaponin A attenuates perimenopausal depression-like symptoms by chronic unpredictable mild stress

行为绝望测验 内科学 内分泌学 神经炎症 原肌球蛋白受体激酶B 尾部悬挂试验 海马体 海马结构 促肾上腺皮质激素 神经营养因子 医学 皮质酮 脑源性神经营养因子 下丘脑 心理学 抗抑郁药 激素 受体 炎症
作者
Xueqin Chen,Shujiao Chen,Wenna Liang,Miao Wang,Cheng‐Fu Li,Shuangshuang Wang,Shuqi Dong,Li‐Tao Yi,Candong Li
出处
期刊:Neuroscience Letters [Elsevier BV]
卷期号:662: 283-289 被引量:62
标识
DOI:10.1016/j.neulet.2017.09.046
摘要

Accumulating studies have shown that a traditional Chinese decoction Chaihu-Shugan-San produced the antidepressant-like effects in rodents including in perimenopausal. Previous studies and our preliminary study indicated that saikosaponin A, one of the main constituents of Chaihu-Shugan-San, enhanced brain-derived neurotrophic factor (BDNF) expression in rats. Herein, this study aimed to evaluate the antidepressant-like effects of saikosaponin A in perimenopausal rats exposed to chronic unpredictable mild stress (CUMS). The sucrose preference test, novelty-suppressed feeding test and forced swimming test were performed after administration of saikosaponin A for 4 weeks. Serum corticotrophin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH) and corticosterone levels, as well as hypothalamus CRH and hippocampal glucocorticoid receptor were measured. In addition, pro-inflammatory cytokines such as interleukin-1beta (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α) in the hippocampus were detected for evaluation of the neuroinflammation. Further, BDNF levels and its receptor TrkB were also determined. Our results indicated that four-week treatment with saikosaponin A increased sucrose preference, decreased latency to feed in the novelty-suppressed feeding test and reduced the immobility time in the forced swimming test. In addition, saikosaponin A restored the dsyregulation of HPA axis and neuroinflammation in rats exposed to CUMS. Moreover, saikosaponin A promoted BDNF-TrkB signaling in the hippocampus. This study demonstrates that saikosaponin A produced the antidepressant-like effects in rats, which may be mediated by restoration of neuroendocrine, neuroinflammation and neurotrophic systems in the hippocampus during perimenopausal.

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