Abstract
Glycine is a well-documented cytoprotective agent. However, whether it has a protective effect against myocardial ischemia-reperfusion injury in vivo is still unknown. By using an open-chest anesthetized rat model, we found that glycine reduced the infarct size by 21% in ischemia-reperfusion injury rats compared with that in the vehicle-treated MI/R rats. The left ventricular ejection fraction and fractional shortening were increased by 19.11% and 30.98%, respectively, in glycine-treated rats. The plasma creatine kinase levels in ischemia-reperfusion injury rats decreased following glycine treatment. Importantly, administration of glycine significantly inhibited apoptosis in post-ischemia-reperfusion myocardium, which was accompanied by suppression of phosphorylated p38 mitogen-activated protein kinase and c-Jun NH2-terminal kinase, as well as the Fas ligand. These results suggest that glycine attenuates myocardial ischemia-reperfusion injury in vivo by inhibiting cardiomyocytes apoptosis. © 2012 The Editorial Board of Journal of Biomedical Research.
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Zhong, X., Li, X., Qian, L., Xu, Y., Lu, Y., Zhang, J., … Chen, Q. (2012). Glycine attenuates myocardial ischemia - reperfusion injury by inhibiting myocardial apoptosis in rats. Journal of Biomedical Research, 26(5), 346–354. https://doi.org/10.7555/JBR.26.20110124
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