Jiang Bo, Wang Ying-Jie, Wang Hao, Song Lu, Huang Chao, Zhu Qing, Wu Feng, Zhang Wei
Department of Pharmacology, Pharmacy College, Nantong University, Nantong, Jiangsu, China.
Provincial key laboratory of Inflammation and Molecular Drug Target, Nantong, Jiangsu, China.
Br J Pharmacol. 2017 Jan;174(2):177-194. doi: 10.1111/bph.13668. Epub 2016 Dec 9.
Depression is a neuropsychiatric disorder accompanied by a decrease in the brain-derived neurotrophic factor (BDNF) signalling cascade in the hippocampus. Fenofibrate is a selective agonist of PPAR-α. In this study, we investigated the antidepressant-like effects of fenofibrate in C57BL/6J mice.
The antidepressant-like effects of fenofibrate were first identified in the forced swim test (FST) and tail suspension test (TST), and then assessed in the chronic social defeat stress (CSDS) model. The changes in the hippocampal BDNF signalling pathway and adult hippocampal neurogenesis after CSDS and fenofibrate treatment were further investigated. A PPAR-α inhibitor, cannabinoid system inhibitors and BDNF signalling inhibitors were also used to determine the antidepressant mechanisms of fenofibrate.
Fenofibrate administration exhibited antidepressant-like effects in the FST and TST without affecting the locomotor activity of mice. Chronic fenofibrate treatment also prevented the depressive-like symptoms induced by CSDS. Moreover, fenofibrate restored the CSDS-induced decrease in the hippocampal BDNF signalling cascade and adult hippocampal neurogenesis. The antidepressant-like effects of fenofibrate could be blocked by a PPAR-α inhibitor and BDNF signalling inhibitors.
Taken together, these results suggest that fenofibrate has antidepressant-like effects mediated through the promotion of the hippocampal BDNF signalling cascade.
抑郁症是一种神经精神疾病,伴有海马体中脑源性神经营养因子(BDNF)信号级联反应的减少。非诺贝特是过氧化物酶体增殖物激活受体-α(PPAR-α)的选择性激动剂。在本研究中,我们调查了非诺贝特对C57BL/6J小鼠的抗抑郁样作用。
首先在强迫游泳试验(FST)和悬尾试验(TST)中确定非诺贝特的抗抑郁样作用,然后在慢性社会挫败应激(CSDS)模型中进行评估。进一步研究CSDS和非诺贝特治疗后海马体BDNF信号通路和成年海马体神经发生的变化。还使用了PPAR-α抑制剂、大麻素系统抑制剂和BDNF信号抑制剂来确定非诺贝特的抗抑郁机制。
给予非诺贝特在FST和TST中表现出抗抑郁样作用,且不影响小鼠的运动活性。长期给予非诺贝特还可预防CSDS诱导的抑郁样症状。此外,非诺贝特恢复了CSDS诱导的海马体BDNF信号级联反应和成年海马体神经发生的减少。非诺贝特的抗抑郁样作用可被PPAR-α抑制剂和BDNF信号抑制剂阻断。
综上所述,这些结果表明非诺贝特具有通过促进海马体BDNF信号级联反应介导的抗抑郁样作用。