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Modulation of GH/IGF-1 axis: potential strategies to counteract sarcopenia in older adults
Authors:Giovannini Silvia  Marzetti Emanuele  Borst Stephen E  Leeuwenburgh Christiaan
Affiliation:a Department of Aging and Geriatric Research, Division of Biology of Aging, Genomics and Biomarkers Core of The Institute on Aging, University of Florida, Gainesville, USA
b Department of Gerontology, Geriatrics and Physiatrics, Catholic University of the Sacred Heart, Rome, Italy
c Malcom Randall Veterans Affairs Medical Center, Geriatric Research, Education and Clinical Center (GRECC), Gainesville, FL 32608-1135, USA
Abstract:Aging is associated with progressive decline of skeletal muscle mass and function. This condition, termed sarcopenia, is associated with several adverse outcomes, including loss of autonomy and mortality. Due to the high prevalence of sarcopenia, a deeper understanding of its pathophysiology and possible remedies represents a high public health priority. Evidence suggests the existence of a relationship between declining growth hormone (GH) and insulin-like growth factor-1 (IGF-1) levels and age-related changes in body composition and physical function. Therefore, the age-dependent decline of GH and IGF-1 serum levels may promote frailty by contributing to the loss of muscle mass and strength. Preclinical studies showed that infusion of angiotensin II produced a marked reduction in body weight, accompanied by decreased serum and muscle levels of IGF-1. Conversely, overexpression of muscle-specific isoform of IGF-1 mitigates angiotensin II-induced muscle loss. Moreover, IGF-1 serum levels have been shown to increase following angiotensin converting enzyme inhibitors (ACEIs) treatment. Here we will review the most recent evidence regarding age-related changes of the GH/IGF-1 axis and its modulation by several interventions, including ACEIs which might represent a potential novel strategy to delay the onset and impede the progression of sarcopenia.
Keywords:Aging   Sarcopenia   GH/IGF-1 axis   Angiotensin   ACE-inhibitors
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