Key result
CB2 agonist AM1241 improves LVEF and reduces post-infarct myocardial fibrosis via PI3K/Akt/Nrf2 signaling.
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Cannabinoid receptor type 2 (CB2) activation is recently reported to promote proliferation of some types of resident stem cells (e.g., hematopoietic stem/progenitor cell or neural progenitor cell). Resident cardiac progenitor cell (CPC) activation and proliferation are crucial for endogenous cardiac regeneration and cardiac repair after myocardial infarction (MI). This study aims to explore the role and possible mechanisms of CB2 receptor activation in enhancing myocardial repair. Our results revealed that CB2 receptor agonist AM1241 can significantly increase CPCs by c-kit and Runx1 staining in ischemic myocardium as well as improve cardiomyocyte proliferation. AM1241 also decreased serum levels of MDA, TNF-α and IL-6 after MI. In addition, AM1241 can ameliorate left ventricular ejection fraction and fractional shortening, and reduce fibrosis. Moreover, AM1241 treatment markedly increased p-Akt and HO-1 expression, and promoted Nrf-2 nuclear translocation. However, PI3K inhibitor wortmannin eliminated these cardioprotective roles of AM1241. In conclusion, AM1241 could induce myocardial regeneration and improve cardiac function, which might be associated with PI3K/Akt/Nrf2 signaling pathway activation. Our findings may provide a promising strategy for cardiac endogenous regeneration after MI.
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Wang et al. (2014) studied Myocardial infarction (mouse model). AM1241 (CB2 receptor agonist) vs. Control / PI3K inhibitor wortmannin was evaluated on Resident cardiac progenitor cell (CPC) activation, cardiomyocyte proliferation, and left ventricular function (LVEF and fractional shortening). CB2 receptor agonist AM1241 significantly increased cardiac progenitor cells, improved LVEF and fractional shortening, and reduced fibrosis in mouse infarcted hearts via PI3K/Akt/Nrf2 signaling.
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