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Ass. Lect. Heba Salem Salem Salem Youssef :: Publications:

Title:
Targeting PPARγ/ Irisin pathway in the Potential Effect of Metformin on D-Galactose-Induced Hepatic Aging in Rats
Authors: Heba S.Youssef , Reham M. Ibrahim, Mahmoud M. Hassan, Marwa Hassan Muhammed, Alaa El-Deen A. El-talees
Year: 2022
Keywords: Hepatic aging, D- gal, Metformin, PPARγ, Irisin
Journal: Not Available
Volume: Not Available
Issue: Not Available
Pages: Not Available
Publisher: Not Available
Local/International: Local
Paper Link: Not Available
Full paper Heba Salem Salem Salem Youssef_BMFJ2543841660341600.pdf
Supplementary materials Not Available
Abstract:

Background: Aging-related changes in liver alter both hepatic structure and function, thus, increasing the mortality rate in susceptible old patients. Metformin provide health benefits to elderly individuals when ingested in appropriate amounts and it is one of the physiological triggers of Peroxisome Proliferator- Activated Receptor- Gamma (PPARγ) and Irisin. Aim: This study aimed to investigate the effect of metformin on hepatic aging induced by Dgalactose (D- gal) in rats, clarifying the role of PPARγ/ Irisin pathway in this process. Methods: 24 adult Wister albino male rats divided into 4 groups: group I (control group): rats received saline; ip, group II (D- gal group): rats received D- gal; ip, group III (Metformin group): rats received Metformin orally & group IV (Metformin + Dgal group): rats received D- gal with Metformin. At the end of experiment, the serum samples were taken for biochemical estimation of Alanine aminotransferase (ALT), Aspartate aminotransferase (AST), Albumin and hepatic tissue PPARγ and Irisin protein levels. Results: compared to control group, D- gal caused hepatic injury confirmed by a significant increase in ALT and AST with a significant decrease in Albumin. Metformin in group IV prevented these changes through increased hepatic PPARγ and Irisin. Conclusion: Metformin showed a protective effect against the D- gal induced hepatic aging through induction of hepatic PPARγ and Irisin.

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