Molecular Mechanisms Underlying Cardiac Adaptation to Exercise

被引:215
作者
Vega, Rick B. [1 ]
Konhilas, John P. [2 ]
Kelly, Daniel P. [1 ]
Leinwand, Leslie A. [3 ]
机构
[1] Sanford Burnham Prebys Med Discovery Inst Lake No, Ctr Metab Origins Dis, Orlando, FL 32827 USA
[2] Univ Arizona, Dept Physiol, Sarver Mol Cardiovasc Res Program, Tucson, AZ 85724 USA
[3] Univ Colorado, BioFrontiers Inst, Mol Cellular & Dev Biol, Boulder, CO 80309 USA
基金
美国国家卫生研究院;
关键词
HEART-FAILURE IMPLICATIONS; ACTIVATED PROTEIN-KINASE; CORONARY-ARTERY-DISEASE; SKELETAL-MUSCLE; ATHLETES HEART; GENE-EXPRESSION; PPAR-ALPHA; CARDIOVASCULAR ADAPTATIONS; VOLUNTARY EXERCISE; GENDER-DIFFERENCES;
D O I
10.1016/j.cmet.2017.04.025
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Exercise elicits coordinated multi-organ responses including skeletal muscle, vasculature, heart, and lung. In the short term, the output of the heart increases to meet the demand of strenuous exercise. Long-term exercise instigates remodeling of the heart including growth and adaptive molecular and cellular re-programming. Signaling pathways such as the insulin-like growth factor 1/PI3K/Akt pathway mediate many of these responses. Exercise-induced, or physiologic, cardiac growth contrasts with growth elicited by pathological stimuli such as hypertension. Comparing the molecular and cellular underpinnings of physiologic and pathologic cardiac growth has unveiled phenotype-specific signaling pathways and transcriptional regulatory programs. Studies suggest that exercise pathways likely antagonize pathological pathways, and exercise training is often recommended for patients with chronic stable heart failure or following myocardial infarction. Herein, we summarize the current understanding of the structural and functional cardiac responses to exercise as well as signaling pathways and downstream effector molecules responsible for these adaptations.
引用
收藏
页码:1012 / 1026
页数:15
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