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Advances in the study of nicotinamide adenine dinucleotide phosphate oxidase in myocardial remodeling

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FRONTIERS MEDIA SA
DOI: 10.3389/fcvm.2022.1000578

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heart failure; myocardial remodeling; NADPH oxidase; reactive oxygen species; oxidative stress

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Myocardial remodeling is the key pathophysiological basis of heart failure. Research has found that the NOXs play an important role in myocardial remodeling and their regulatory mechanisms may be promising therapeutic targets for the treatment of heart failure.
Myocardial remodeling is a key pathophysiological basis of heart failure, which seriously threatens human health and causes a severe economic burden worldwide. During chronic stress, the heart undergoes myocardial remodeling, mainly manifested by cardiomyocyte hypertrophy, apoptosis, interstitial fibrosis, chamber enlargement, and cardiac dysfunction. The NADPH oxidase family (NOXs) are multisubunit transmembrane enzyme complexes involved in the generation of redox signals. Studies have shown that NOXs are highly expressed in the heart and are involved in the pathological development process of myocardial remodeling, which influences the development of heart failure. This review summarizes the progress of research on the pathophysiological processes related to the regulation of myocardial remodeling by NOXs, suggesting that NOXs-dependent regulatory mechanisms of myocardial remodeling are promising new therapeutic targets for the treatment of heart failure.

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