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Among different sources that contribute in the global oxidative stress, the vast majority of cellular reactive oxygen species (ROS) originate from mitochondrial compartments.Recently, monoamine oxidases (MAOs) are identified as a prominent source of ROS.Monoamine oxidases are localized in the outer membrane of mitochondria and exist as two different isoforms, MAO-A and MAO-B.MAOs are mitochondrial flavoenzymes responsible for oxidative deamination of biogenic amines and during this process, H 2 O 2 and aldehydes are generated as intermediate products.The role of monoamine oxidase in cardiovascular pathophysiology has only recently gained some attention as it is demonstrated that H 2 O 2 and aldehydes may target myocardial function and consequently cardiac function.Results obtained by different research groups showed that MAO-A plays a key role in the regulation of physiological cardiac function and in the development of acute and chronic heart diseases through two mechanisms: regulation of substrate concentration and intracellular production of ROS.In this review, we will focus on the role of MAO-A in the field of cardiac aging and related diseases.
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Datta et al. (2020) studied this question.
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