| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2027647 | Steroids | 2015 | 6 Pages |
•Depression is a chronic, multi-factorial psychiatric disorder.•Repeated CORT administration develops depression-like behavior in mice.•Resveratrol ameliorates CORT-induced depression-like behavior.•Resveratrol acts via upregulation of BDNF levels and by regulation of HPA axis.
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.
