Hormonal control of aging in rodents: The somatotropic axis

被引:60
作者
Brown-Borg, Holly M. [1 ]
机构
[1] Univ ofNorth Dakota, Sch Med & Hlth Sci, Dept Pharmacol Physiol & Therapeut, Grand Forks, ND 58203 USA
关键词
Growth hormone; IGF-1; Stress resistance; Aging; GROWTH-FACTOR-I; AMES DWARF MICE; RECEPTOR/BINDING PROTEIN GENE; LIFE-SPAN EXTENSION; TRANSGENIC MICE; BODY-COMPOSITION; OXIDATIVE STRESS; INSULIN SENSITIVITY; SKELETAL-MUSCLE; KNOCKOUT MICE;
D O I
10.1016/j.mce.2008.07.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
There is a growing body of literature focusing on the somatotropic axis and regulation of aging and type animals with normal plasma hormone concentrations. This information, along with that found in longevity. Many of these reports derive data from multiple endocrine mutants, those that exhibit both elevated growth hormone (GH) and insulin-like growth factor I (IGF-1) or deficiencies in one or both of these hormones. In general, both spontaneous and genetically engineered GH and IGF-1 deficiencies have lead to small body size, delayed development of sexual maturation and age-related pathology, and life span extension. In contrast, characteristics of high circulating GH included larger body sizes, early puberty and reproductive senescence, increased cancer incidence and reduced life span when compared to wildtype other species, implicates this anabolic pathway as the major regulator of longevity in animals. (C) 2008 Published by Elsevier Ireland Ltd.
引用
收藏
页码:64 / 71
页数:8
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