Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share By
Administration of 5-Hydroxydecanoate, a Selective Inhibitor of Mitochondrial Atp-Sensitive Potassium Channels, Inhibits Apelin-Induced Cardioprotection in Ischemia/Reperfusion Model of Male Rats



Chookalaei LG1 ; Imani A1 ; Faghihi M1 ; Azizi Y2 ; Rajani SF1
Authors

Source: Indian Journal of Physiology and Pharmacology Published:2017

Abstract

Apelin, a recently discovered endogenous peptide has shown to protect myocardium against infarction in the animal model. The aim of this study was to evaluate the effects of mitochondrial ATP-sensitive potassium channels inhibition on myocardial protection afforded by apelin treatment during ischemia period. Thirty-two male Wistar rats were divided into four groups; (1) Ischemia/reperfusion, (2) Apelin + ischemia/reperfusion, (3) 5-hydroxydecanoate + Apelin + ischemia/reperfusion and (4) 5-hydroxydecanoate + ischemia/reperfusion. Hemodynamic parameters and infarct size were measured for all groups. There were no significant differences in hemodynamic functions during ischemia and reperfusion periods between the experimental groups. Further, there was a decrease in infarct size in apelin group when compared to ischemia/reperfusion group. However, selective inhibition of mitochondrial ATP-sensitive potassium channels by administration of 5-hydroxydecanoate, diminished the infarct-sparing effect of apelin. These findings suggest that apelin-induced protection was removed by using 5-hydroxydecanoate as a selective inhibitor of mitochondrial ATP-sensitive potassium channel. © 2017, Association of Physiologists and Pharmacologists of India. All rights reserved.
Other Related Docs
10. The Footprint of Kynurenine Pathway in Cardiovascular Diseases, International Journal of Tryptophan Research (2022)
20. Mitochondrial Quality Control and Melatonin: A Strategy Against Myocardial Injury, Journal of Biochemical and Molecular Toxicology (2025)