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The potential of aldehyde dehydrogenase 2 as a therapeutic target in cardiovascular disease
被引:27
|作者:
Muenzel, Thomas
[1
,2
,3
]
Daiber, Andreas
[1
,2
,3
]
机构:
[1] Johannes Gutenberg Univ Mainz, Med Ctr, Cardiol 1, Ctr Cardiol, Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Med Ctr, CTH, Mainz, Germany
[3] German Ctr Cardiovasc Res DZHK, Partner Site Rhine Main, Mainz, Germany
关键词:
Cardiovascular protection;
mitochondrial aldehyde dehydrogenase;
alcoholism;
organic nitrate bioactivation;
oxidative stress;
reactive aldehydes;
CORONARY-ARTERY-DISEASE;
MYOCARDIAL ISCHAEMIA/REPERFUSION INJURY;
MANGANESE SUPEROXIDE-DISMUTASE;
MITOCHONDRIAL OXIDATIVE STRESS;
INDUCED CARDIAC DYSFUNCTION;
ALDH2;
RS671;
POLYMORPHISM;
NITRATE TOLERANCE;
GLU504LYS POLYMORPHISM;
ORGANIC NITRATES;
ALDEHYDE-DEHYDROGENASE-2;
GENE;
D O I:
10.1080/14728222.2018.1439922
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Introduction: Mitochondrial aldehyde dehydrogenase (ALDH-2) plays a major role in the ethanol detoxification pathway by removing acetaldehyde. Therefore, ALDH-2 inhibitors such as disulfiram represent the first therapeutic targeting of ALDH-2 for alcoholism therapy. Areas covered: Recently, ALDH-2 was identified as an essential bioactivating enzyme of the anti-ischemic organic nitrate nitroglycerin, bringing ALDH-2 again into the focus of clinical interest. Mechanistic studies on the nitroglycerin bioactivation process revealed that during bioconversion of nitroglycerin and in the presence of reactive oxygen and nitrogen species the active site thiols of ALDH-2 are oxidized and the enzyme activity is lost. Thus, ALDH-2 activity represents a useful marker for cardiovascular oxidative stress, a concept, which has been meanwhile supported by a number of animal disease models. Mechanistic studies on the protective role of ALDH-2 in different disease processes identified the detoxification of 4-hydroxynonenal by ALDH-2 as a fundamental process of cardiovascular, cerebral and antioxidant protection. Expert opinion: The most recent therapeutic exploitation of ALDH-2 includes activators of the enzyme such as Alda-1 but also cell-based therapies (ALDH-bright cells) that deserve further clinical characterization in the future.
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页码:217 / 231
页数:15
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