Effect of irisin on metabolic and platelet functions in type 2 diabetic rats: role of soluble receptor of advanced glycation end products (sRAGE)

Beni-Suef University Journal of Basic and Applied Sciences

Hossam E. Salah¹  Samia Hussein²  Nanees F. El-Malkey³  Sherif W. Mansour³  Mai M. Hasan³  Talal El-Deep³ 

[1] Clinical Pathology Department, Faculty of Medicine, Zagazig University;Medical Biochemistry and Molecular Biology, Faculty of Medicine, Zagazig University;Physiology Department, Faculty of Medicine, Zagazig University;

关键词: Diabetes;    Irisin;    Platelet;    sRAGE;    Hyperglycemia;    Inflammation;   

DOI  :  10.1186/s43088-021-00148-1

来源: DOAJ

【 摘 要 】

Abstract Background Irisin is an adipomyokine with a promising potential for the treatment of metabolic disturbances and endothelial dysfunction. This study aimed to explore the effect of irisin on metabolic and platelet functions, and to explore the possible involvement of soluble receptor of advanced glycation end product (sRAGE) in the type 2 diabetes mellitus (T2DM) rat model. Thirty-three adult male albino rats were divided into three groups: normal control, vehicle-treated T2DM group, and irisin-treated T2DM. At the end of the study period, metabolic parameters, platelet count, mean platelet volume, platelet distribution width, plateletcrit, and serum sRAGE were determined. Results Irisin significantly improved platelet function and metabolic derangements induced by T2DM and significantly increased sRAGE. sRAGE was significantly negatively associated with platelet function parameters and some glucometabolic parameters. Additionally, mean platelet volume showed a significant predictive value for the change in serum sRAGE. Conclusions Irisin could have a protective role against diabetes-induced platelet dysfunction by increasing sRAGE levels, indicating the potential beneficial effects of sRAGE in the type 2 diabetic rat model.

【 授权许可】

Unknown