| Literature DB >> 29856969 |
Shumiao Zhang1, Yaguang Zhou1, Lei Zhao2, Xin Tian3, Min Jia1, Xiaoming Gu1, Na Feng1, Rui An4, Lu Yang1, Guoxu Zheng1, Juan Li1, Haitao Guo1, Rong Fan5, Jianming Pei6.
Abstract
This study aims to investigate the effect of κ-opioid receptor activation on myocardial ischemia and reperfusion(I/R) injury and elucidate the underlying mechanisms. Myocardial I/R rat model and simulated I/R cardiomyocytes model were established. In vivo study showed that U50,488 H improved cardiac function, reduced myocardial infarct size and serum cTnT significantly. The effect of U50,488 H was abolished by nor-BNI(a κ-opioid receptor antagonist), Compound C(an AMPK inhibitor), Akt inhibitor and L-NAME(an eNOS inhibitor). AICAR, an AMPK activator, mimicked the effect of U50,488 H. U50,488 H up-regulated p-AMPK, p-Akt, and p-eNOS, which were abolished by nor-BNI. AICAR increased p-Akt and p-eNOS, which was abolished by Compound C. In vitro study showed that U50,488 H increased p-AMPK, p-Akt, and p-eNOS via κ-OR activation. The effect of U50,488 H on p-AMPK was abolished by compound C, but not Akt inhibitor and L-NAME. The effect of U50,488 H on p-Akt was abolished by compound C and Akt inhibitor, but not L-NAME. AICAR increased p-Akt and p-eNOS, which was abolished by Akt inhibitor, but not L-NAME. U50,488 H and AICAR also increased the viability of cardiomyocytes subjected to simulated I/R, the effects of U50,488 H and AICAR were blocked by nor-BNI, Compound C, Akt inhibitor, and L-NAME, respectively. In conclusion, κ-OR activation confers cardioprotection via AMPK/Akt/eNOS signaling.Entities:
Keywords: AICAR(PubChem CID: 266934); AMPK/Akt/eNOS signaling; Compound C (PubChem CID:11524144); L-NAME (PubChem CID: 39836); Myocardial ischemia-reperfusion injury; U50,488 H (PubChem CID: 135349); nor-BNI (PubChem CID: 5480230); κ-opioid receptor
Mesh:
Substances:
Year: 2018 PMID: 29856969 DOI: 10.1016/j.ejphar.2018.05.043
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432