4.7 Article

8-Gingerol Ameliorates Myocardial Fibrosis by Attenuating Reactive Oxygen Species, Apoptosis, and Autophagy via the PI3K/Akt/mTOR Signaling Pathway

期刊

FRONTIERS IN PHARMACOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.711701

关键词

8-gingerol; myocardial fibrosis; reactive oxygen species; apoptosis; autophagy; PI3K/Akt/mTOR signaling pathway

资金

  1. Excellent Youth Program of Hebei University of Chinese Medicine [YQ2020003]
  2. Project of Science and Technology Research Project of Hebei Province [BJ2020002]

向作者/读者索取更多资源

8-gingerol (8-Gin) is a phenolic substance extracted from ginger that has been shown to have multiple pharmacological properties. This study found that 8-Gin can reduce J-point elevation and heart rate, decrease cardiac weight index and left ventricle weight index, suppress ROS generation, attenuate ISO-induced heart damage, lower collagen levels, inhibit autophagosome formation, modulate protein activities related to apoptosis, and increase expressions of the PI3K/Akt/mTOR signaling pathway. These findings suggest that 8-Gin may exert cardioprotective effects against myocardial fibrosis by inhibiting ROS generation, apoptosis, and autophagy through modulation of the PI3K/Akt/mTOR signaling pathway.
8-gingerol (8-Gin) is the series of phenolic substance that is extracted from ginger. Although many studies have revealed that 8-Gin has multiple pharmacological properties, the possible underlying mechanisms of 8-Gin against myocardial fibrosis (MF) remains unclear. The study examined the exact role and potential mechanisms of 8-Gin against isoproterenol (ISO)-induced MF. Male mice were intraperitoneally injected with 8-Gin (10 and 20 mg/kg/d) and concurrently subcutaneously injected with ISO (10 mg/kg/d) for 2 weeks. Electrocardiography, pathological heart morphology, myocardial enzymes, reactive oxygen species (ROS) generation, degree of apoptosis, and autophagy pathway-related proteins were measured. Our study observed 8-Gin significantly reduced J-point elevation and heart rate. Besides, 8-Gin caused a marked decrease in cardiac weight index and left ventricle weight index, serum levels of creatine kinase and lactate dehydrogenase (CK and LDH, respectively), ROS generation, and attenuated ISO-induced pathological heart damage. Moreover, treatment with 8-Gin resulted in a marked decrease in the levels of collagen types I and III and TGF-beta in the heart tissue. Our results showed 8-Gin exposure significantly suppressed ISO-induced autophagosome formation. 8-Gin also could lead to down-regulation of the activities of matrix metalloproteinases-9 (MMP-9), Caspase-9, and Bax protein, up-regulation of the activity of Bcl-2 protein, and alleviation of cardiomyocyte apoptosis. Furthermore, 8-Gin produced an obvious increase in the expressions of the PI3K/Akt/mTOR signaling pathway-related proteins. Our data showed that 8-Gin exerted cardioprotective effects on ISO-induced MF, which possibly occurred in connection with inhibition of ROS generation, apoptosis, and autophagy via modulation of the PI3K/Akt/mTOR signaling pathway.

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