作者: Patrice Delafontaine , Marijke Brink , Yao-Hua Song
DOI: 10.1007/978-1-59259-795-6_17
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摘要: The RAS and the IGF-I system interact at multiple levels to regulate physiological pathological cardiac growth responses. IGF-I promotes survival of skeletal muscle which is salutary in heart failure. AngII down regulates circulating IGF binding proteins, leading increased myocardial apoptosis proteolysis. Preliminary studies reveal significant alterations failure. An imbalance between contributes progression from compensated decompensated failure.