Abstract

Depression is a psychiatric disorder characterized by low-esteem, anhedonia, social deficit, and lack of interest. Decreased brain-derived neurotrophic factor (BDNF) and impaired tropomyosin kinase B receptor (TrkB receptor) signaling are associated with depression. In our study, depressive-like behavior was induced in mice by chronic unpredictable mild stress (CUMS) model. Various behavioral tests like tail suspension test (TST), open field test (OFT), sucrose preference test (SPT); biochemical analyses for corticosterone, reduced glutathione (GSH), lipid peroxidation (LPO), superoxide dismutase (SOD), nitric oxide (NO) and enzyme-linked immunosorbent assay (ELISA) for BDNF were performed. Body weight was measured every week. CUMS induced depressive-like behavior was found to be associated with increased oxidative stress in the brain and serum corticisterone with subsequent reduction of BDNF. Sodium orthovanadate (SOV), a protein tyrosine phosphatase inhibitor already reported to elevate BDNF levels, was used as the test drug. Sodium orthovanadate (5 mg/kg, 10 mg/kg) and fluoxetine (FLX-10 mg/kg) was given to mice orally for 21days before 30 min of stress induction. The behavioral tests reflected depressive-like behavior in CUMS, which was attenuated by both SOV and fluoxetine. SOV at 10 mg/kg demonstrated significant results in the present study characterized by decreased malondialdehyde levels (MDA/LPO), NO levels, and increased GSH level and SOD activity in both the cortex and hippocampus. Besides, ELISA has revealed the significant elevation of BDNF levels in the treatment groups (SOV-5 mg/kg, 10 mg/kg and FLX-10 mg/kg) as compared to the disease group (CUMS). Therefore, the treatment with SOV appeared to reverse both oxidative and nitrosative stress. Decreased serum corticosterone levels observed with SOV (5 & 10 mg/kg), FLX-10 mg/kg, FLX (10 mg/kg) + SOV (5 mg/kg); and SOV-10 mg/kg per-se treatment and elevated BDNF level with SOV (5 & 10 mg/kg), FLX-10 mg/kg were associated with attenuation of depressive-like behavior. The findings of this preliminary study indicate that SOV has the potential to restore antidepressant-like effects or prevent stress-induced anhedonia and so further molecular mechanisms are warranted for clinical translation.

Highlights

  • Major Depressive Disorder (MDD) is one of the most prevalent, recurrent, and debilitating psychopathology forms

  • Treatment with sodium orthovanadate (SOV) (10 mg/kg) and fluoxetine significantly increased the ambulatory score when compared to Chronic unpredictable mild stress (CUMS) group (p < 0.05)

  • Treatment with a combination group showed no significant difference in the ambulatory score than the CUMS and control group

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Summary

Introduction

Major Depressive Disorder (MDD) is one of the most prevalent, recurrent, and debilitating psychopathology forms. 30–50% of patients don't even respond to their initial antidepressant trial, and the remission rates are as low as 37.5% [2] This phenomenon probably results from the complex and multifactorial MDD etiology, which comprises psychosocial, biological, environmental, and genetic factors, explaining why most patients fail to respond to the standard monoaminergic antidepressants [3]. This limitation led to a paradigm shift towards the neurotrophin hypothesis, as depression is associated with neuronal atrophy and neuronal loss in specific brain regions in several clinical and preclinical studies [4, 5]

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