Resveratrol ameliorates depressive-like behavior in repeated corticosterone-induced depression in mice

皮质酮 内分泌学 行为绝望测验 内科学 白藜芦醇 海马体 抗抑郁药 氟西汀 海马结构 尾部悬挂试验 神经营养因子 脑源性神经营养因子 糖皮质激素 化学 血清素 心理学 医学 药理学 激素 受体
作者
Syed Hamid Ali,Rajaram Mohanrao Madhana,K V Athira,Eshvendar Reddy Kasala,Lakshmi Narendra Bodduluru,Sathish Pitta,Jalandhar Reddy Mahareddy,Mangala Lahkar
出处
期刊:Steroids [Elsevier BV]
卷期号:101: 37-42 被引量:123
标识
DOI:10.1016/j.steroids.2015.05.010
摘要

A mouse model of depression has been recently developed by exogenous corticosterone (CORT) administration, which has shown to mimic HPA-axis induced depression-like state in animals. The present study aimed to examine the antidepressant-like effect and the possible mechanisms of resveratrol, a naturally occurring polyphenol of phytoalexin family, on depressive-like behavior induced by repeated corticosterone injections in mice. Mice were injected subcutaneously (s.c.) with 40 mg/kg corticosterone (CORT) chronically for 21 days. Resveratrol and fluoxetine were administered 30 min prior to the CORT injection. After 21-days treatment with respective drugs, behavioral and biochemical parameters were estimated. Since brain derived neurotrophic factor (BDNF) has been implicated in antidepressant activity of many drugs, we also evaluated the effect of resveratrol on BDNF in the hippocampus. Three weeks of CORT injections in mice resulted in depressive-like behavior, as indicated by the significant decrease in sucrose consumption and increase in immobility time in the forced swim test and tail suspension test. Further, there was a significant increase in serum corticosterone level and a significant decrease in hippocampus BDNF level in CORT-treated mice. Treatment of mice with resveratrol significantly ameliorated all the behavioral and biochemical changes induced by corticosterone. These results suggest that resveratrol produces an antidepressant-like effect in CORT-induced depression in mice, which is possibly mediated by rectifying the stress-based hypothalamic–pituitary–adrenal (HPA) axis dysfunction paradigm and upregulation of hippocampal BDNF levels.

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