Signaling effectors underlying pathologic growth and remodeling of the heart

被引:456
作者
van Berlo, Jop H. [1 ]
Maillet, Marjorie [1 ]
Molkentin, Jeffery D. [1 ]
机构
[1] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Howard Hughes Med Inst, Dept Pediat,Div Mol Cardiovasc Biol, Cincinnati, OH 45229 USA
关键词
BETA-ADRENERGIC-RECEPTOR; KINASE-C-ALPHA; LEFT-VENTRICULAR MASS; ENHANCES CARDIAC CONTRACTILITY; PROTEIN-KINASE; HISTONE DEACETYLASE; MYOCARDIAL-INFARCTION; PRESSURE-OVERLOAD; DILATED CARDIOMYOPATHY; HYPERTROPHIC RESPONSE;
D O I
10.1172/JCI62839
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Cardiovascular disease is the number one cause of mortality in the Western world. The heart responds to many cardiopathological conditions with hypertrophic growth by enlarging individual myocytes to augment cardiac pump function and decrease ventricular wall tension. Initially, such cardiac hypertrophic growth is often compensatory, but as time progresses these changes become maladaptive. Cardiac hypertrophy is the strongest predictor for the development of heart failure, arrhythmia, and sudden death. Here we discuss therapeutic avenues emerging from molecular and genetic studies of cardiovascular disease in animal models. The majority of these are based on intracellular signaling pathways considered central to pathologic cardiac remodeling and hypertrophy, which then leads to heart failure. We focus our discussion on selected therapeutic targets that have more recently emerged and have a tangible translational potential given the available pharmacologic agents that could be readily evaluated in human clinical trials.
引用
收藏
页码:37 / 45
页数:9
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