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Mitochondria-targeted agents: Future perspectives of mitochondrial pharmaceutics in cardiovascular diseases

查看全文 作  者:Thekkuttuparambil Ananthanarayanan [1]Ajith;Thankamani Gopinathan [2]Jayakumar 高影响力作者 机构地区:[1]Department of Biochemistry, Amala Institute of Medical Sciences, Thrissur 680 555, Kerala, India;[2]Department of Inter-ventional Cardiology, Amala Cardiac Centre, Thrissur 680 555, Kerala, India高影响力机构 出  处:《World Journal of Cardiology》索引2014年第6卷第10期,共9页高影响力期刊 摘  要:Mitochondria are one of the major sites for the genera-tion of reactive oxygen species(ROS) as an undesirable side product of oxidative energy metabolism. Damaged mitochondria can augment the generation of ROS. Dys-function of mitochondria increase the risk for a large number of human diseases, including cardiovascular diseases(CVDs). Heart failure(HF) following ischemic heart disease, infantile cardiomyopathy and cardiac hypertrophy associated with left ventricular dilations are some of the CVDs in which the role of mitochon-drial oxidative stress has been reported. Advances in mitochondrial research during the last decade focused on the preservation of its function in the myocardium, which is vital for the cellular energy production. Expe-rimental and clinical trials have been conducted using mitochondria-targeted molecules like: MnSOD mimetics, such as EUK-8, EUK-134 and MitoSOD; choline esters of glutathione and N-acetyl-L-cysteine; triphenylphospho-nium ligated vitamin E, lipoic acid, plastoquinone andmitoCoQ10; and Szeto-Schiller(SS)- peptides(SS-02 and SS-31). Although many results are inconclusive, some of the findings, especially on CoQ10, are worthwhile. This review summarizes the role of mitochondria-tar-geted delivery of agents and their consequences in the control of HF. 关 键 词:CARDIOVASCULAR diseases OXIDATIVE stress ANTIOXIDANT Electron transport chain MITOCHONDRIAL medicine Heart failure
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