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Green tea extract and catechin ameliorate chronic fatigue-induced oxidative stress in mice.

Anjali Singal, Surinder Kaur, Naveen Tirkey, Kanwaljit Chopra
Other Journal of medicinal food 2005 40 citations
PubMed DOI
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Study Design

Study Type
In Vitro
Population
Mouse model of chronic fatigue syndrome
Duration
1 weeks
Intervention
Green tea extract and catechin ameliorate chronic fatigue-induced oxidative stress in mice. GTE 25-50 mg/kg or catechin 50-100 mg/kg
Comparator
Saline-treated fatigued mice
Primary Outcome
Immobility time, lipid peroxidation, glutathione
Effect Direction
Positive
Risk of Bias
Unclear

Abstract

Chronic fatigue syndrome (CFS) is an illness characterized by persistent and relapsing fatigue, often accompanied by numerous symptoms involving various body systems. The etiology of CFS remains unclear, but a number of studies have shown that oxidative stress may be involved in its pathogenesis. The present study was designed to investigate the protective effect of green tea extract (GTE) and catechin in the mouse model of CFS. Animals were subjected to a forced swimming test session of 6 minutes every day for 7 days; a significant increase in immobility time on successive days represented the CFS in mice. Biochemical analysis revealed that the chronic swim test significantly increased lipid peroxidation levels and decreased glutathione levels in mouse whole-brain homogenate. Treatment with GTE (25 or 50 mg/kg, i.p.) and catechin (50 or 100 mg/kg, i.p.) for 7 days reversed the increase in immobility time. Protection was correlated with the lowered levels of lipid peroxidation and restoration of reduced glutathione levels in the brains of fatigued mice. These findings strongly suggest the pivotal role of oxidative stress in the pathophysiology of CFS and that GTE and catechin could be used as potential agents in the management of CFS and warrant the inclusion of GTE and catechin in the treatment regimen of CFS patients.

TL;DR

The findings of this study strongly suggest the pivotal role of oxidative stress in the pathophysiology of CFS and that GTE and catechin could be used as potential agents in the management of C FS and warrant the inclusion ofGTE andcatechin in the treatment regimen ofCFS patients.

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