Literature DB >> 19011280

Effect of Ramadan fasting on markers of oxidative stress and serum biochemical markers of cellular damage in healthy subjects.

Wissam H Ibrahim1, Hosam M Habib, Amjad H Jarrar, Samer A Al Baz.   

Abstract

BACKGROUND/AIMS: Ramadan is a holy month for Muslims during which they abstain from eating, drinking and smoking from dawn to sunset. This makes Ramadan a unique model for studying the effects of altered meal patterns in humans. The aim of this study was to determine the effect of Ramadan fasting on markers of oxidative stress and serum biochemical markers of cellular damage in healthy subjects.
METHODS: Fourteen healthy volunteers (9 men and 5 women aged 25-58 years) who fasted during Ramadan participated in the study. Blood sampling was conducted 2 days before Ramadan and on days 14 and 28 of Ramadan. The following were measured: (1) in serum, malondialdehyde (MDA), aspartate aminotransferase, alanine aminotransferase, creatine kinase, alkaline phosphatase, lactate dehydrogenase, blood urea nitrogen, total proteins, uric acid, albumin, glucose, triglycerides and total cholesterol; (2) in plasma, protein-bound carbonyls, alpha-tocopherol, gamma-tocopherol, retinol, vitamin C and carotenoids, and (3) in erythrocytes, MDA, glutathione, glutathione peroxidase and catalase.
RESULTS: Erythrocyte MDA, serum glucose and triglycerides and plasma total carotenoids were significantly lower (p<0.05) on day 28 of Ramadan compared to before Ramadan. The rest of the variables were not significantly altered by Ramadan fasting.
CONCLUSION: The results obtained indicate that with the exception of a slight reduction in lipid peroxidative damage in erythrocytes, Ramadan fasting does not alter oxidative stress parameters or biochemical markers of cellular damage in healthy subjects. Copyright 2008 S. Karger AG, Basel.

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Year:  2008        PMID: 19011280     DOI: 10.1159/000172979

Source DB:  PubMed          Journal:  Ann Nutr Metab        ISSN: 0250-6807            Impact factor:   3.374


  26 in total

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