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Effects of Azilsartan, Aliskiren or Their Combination on High Fat Diet-induced Non-alcoholic Liver Disease Model in Rats

Overview
Journal Med Arch
Specialty General Medicine
Date 2017 Oct 5
PMID 28974844
Citations 6
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Abstract

Introduction: In addition to its role in regulation of blood pressure, fluid and electrolyte homeostasis, the renin-angiotensin system (RAS) components were expressed in many other tissues suggesting potential roles in their functions.

Aim: The present study aims to evaluate the protective effect aliskiren, when used alone or in combination with azilsartan against high fat diet-induced liver disease in rats.

Material And Methods: Thirty-two Wistar male rats, weighing 150-200 gm were allocated evenly into four groups and treated as follow: group I, rats were fed a specially formulated high-fat diet for 8 weeks to induce non-alcoholic liver disease and considered as control group; groups II, III and IV, the rats were administered azilsartan (0.5 mg/kg), aliskiren (25 mg/kg) or their combination orally via gavage tube once daily, and maintained on high fat diet for 8 weeks. The possible treatment outcome was evaluated through measuring serum levels of glucose, insulin, lipid profile, TNF-α, IL-1β and liver enzymes. Additionally, the liver tissue contents of glycogen and lipids and histological changes were also evaluated.

Result: The results showed that azilsartan significantly improves the studied markers greater than aliskiren, and their combination o has no additive or synergistic effects on the activity of each one of them.

Conclusion: Both azilsartan and aliskiren protects the rats against high-fat diet induced NAFLD with predominant effects for the former, and their combination showed no beneficial synergistic or additive effects.

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References
1.
Araujo A, Varela H, de Medeiros C, Brito G, de Lima K, de Moura L . Azilsartan reduced TNF-α and IL-1β levels, increased IL-10 levels and upregulated VEGF, FGF, KGF, and TGF-α in an oral mucositis model. PLoS One. 2015; 10(2):e0116799. PMC: 4331549. DOI: 10.1371/journal.pone.0116799. View

2.
Zhao M, Li Y, Wang J, Ebihara K, Rong X, Hosoda K . Azilsartan treatment improves insulin sensitivity in obese spontaneously hypertensive Koletsky rats. Diabetes Obes Metab. 2011; 13(12):1123-9. DOI: 10.1111/j.1463-1326.2011.01471.x. View

3.
Paul M, Poyan Mehr A, Kreutz R . Physiology of local renin-angiotensin systems. Physiol Rev. 2006; 86(3):747-803. DOI: 10.1152/physrev.00036.2005. View

4.
Milic S, Mikolasevic I, Krznaric-Zrnic I, Stanic M, Poropat G, Stimac D . Nonalcoholic steatohepatitis: emerging targeted therapies to optimize treatment options. Drug Des Devel Ther. 2015; 9:4835-45. PMC: 4548724. DOI: 10.2147/DDDT.S64877. View

5.
Takahashi N, Li F, Hua K, Deng J, Wang C, Bowers R . Increased energy expenditure, dietary fat wasting, and resistance to diet-induced obesity in mice lacking renin. Cell Metab. 2007; 6(6):506-12. PMC: 2174204. DOI: 10.1016/j.cmet.2007.10.011. View