Protective Effects of Pterostilbene Against Myocardial Ischemia/Reperfusion Injury in Rats

内科学 超氧化物歧化酶 丙二醛 乳酸脱氢酶 内分泌学 脂质过氧化 白藜芦醇 一氧化氮 抗氧化剂 麻醉
作者
Miao Wu,Shi-Juan Lu,Jiang-hua Zhong,Kang Huang,Saidan Zhang
出处
期刊:Inflammation [Springer Nature]
卷期号:40 (2): 578-588 被引量:15
标识
DOI:10.1007/s10753-016-0504-2
摘要

Pterostilbene (PTB) has been suggested to protect against myocardial ischemia/reperfusion (MI/R) injury. Gas6/Axl signaling has been suggested to play an important role in cell survival. However, the interaction between PTB and Gas6/Axl signaling in MI/R remains unclear. This study aims to evaluate the role of Gas6/Axl signaling in the protective effects of PTB against MI/R injury. In experiment 1, the rats were subjected to 30 min of ischemia, followed by 3, 6, and 12 h of reperfusion, respectively. In experiment 2, the rats were administered intraperitoneally with PTB or vehicle and subjected to MI/R injury. The results suggested that the expression of Gas6 and Axl decreased significantly after MI/R injury. PTB treatment conferred a cardioprotective effect with an improved post-ischemic cardiac function, a reduced myocardial infarct size, and decreased lactate dehydrogenase and creatine kinase-MB in the serum, a decreased oxidative stress and inflammation, and a reduced number of apoptotic cardiomyocytes. Moreover, PTB treatment up-regulated the expression of Gas6, Axl, and Bcl-2 and down-regulated Bax expression. Our findings suggest that PTB treatment exerts cardioprotection against MI/R injury via attenuating inflammatory response, oxidative stress, and apoptosis and up-regulating the expression of Gas6 and Axl. The application of PTB may be a new strategy for the treatment of MI/R injury.
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