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Research Article
4 (
1
); 83-102

The Effect of Orlistat in High-Fat Diet Induced-Obesity in Male Albino Rats.

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This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
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This article was originally published by Qassim University and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Obesity has been considered a global epidemic that needs immediate prevention and control because it causes slew of physiological, psychological, and social problems. The present study aims to investigate the anti-obesity effect of orlistat in male albino rats and investigate the mechanism of its effect. 30 albino male rats weighing between (150 -180 g) were divided into three groups, as following: G I: control group feed normal diet; G II: male albino rats fed with high fat diet for 12 weeks; G III:  male albino rats fed with high fat diet and treated with a daily oral dose of orlistat 50mg/kg/day for 45 days. The administration of a daily HFD to male albino rats for successive 12weeks resulted in obesity that was estimated by calculating BMI and increased levels of serum resistin, leptin , insulin , MDA,  pro-inflammatory cytokines , lipid profiles and decreased levels of serum irisin, early signs of fibrosis suggesting the onset of non-alcoholic steatohepatitis (NASH).Orlistat treatment resulted in weight loss and marked improvement in inflammation by decreasing interleukin1-ß, interleukin-6 , MDA levels and increases levels of serum irisin and effectively reduces fat deposition and inflammation in liver tissue. Orlistat is a lipase inhibitor resulted in weight loss via fat absorption inhibition and decreasing the inflammatory responses resulted from obesity.   Key Words: Obesity, Orlistat, oxidative stress, lipid profile, steatohepatitis, insulin, irisin, resistin, interleukin-6, interleukin 1-ß.


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