Taking pressure off the heart: the ins and outs of atrophic remodelling

被引:45
作者
Baskin, Kedryn K. [1 ]
Taegtmeyer, Heinrich [1 ]
机构
[1] Univ Texas Houston, Sch Med, Div Cardiol, Dept Internal Med, Houston, TX 77030 USA
关键词
Cardiac atrophy; Mechanical unloading; Metabolic unloading; FAILING HUMAN HEART; UBIQUITIN-PROTEASOME SYSTEM; SKELETAL-MUSCLE ATROPHY; ASSIST DEVICE SUPPORT; MECHANICAL CIRCULATORY SUPPORT; LEFT-VENTRICULAR HYPERTROPHY; ACTIVATED RECEPTOR-ALPHA; AORTIC-VALVE-REPLACEMENT; RELOADED CAT MYOCARDIUM; TRANSPLANTED RAT HEARTS;
D O I
10.1093/cvr/cvr060
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Our work on atrophic remodelling of the heart has led us to appreciate the simple principles in biology: (i) the dynamic nature of intracellular protein turnover, (ii) the return to the foetal gene programme when the heart remodels, and (iii) the adaptive changes of cardiac metabolism. Although the molecular mechanisms of cardiac hypertrophy are many, much less is known regarding the molecular mechanisms of cardiac atrophy. We state the case that knowing more about mechanisms of atrophic remodelling may provide insights into cellular consequences of metabolic and haemodynamic unloading of the stressed heart. Overall we strive to find an answer to the question: 'What makes the failing heart shrink and become stronger?' We speculate that signals arising from intermediary metabolism of energy-providing substrates are likely candidates.
引用
收藏
页码:243 / 250
页数:8
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