Does growth hormone prevent or accelerate aging?

被引:96
作者
Bartke, A [1 ]
Brown-Borg, HM
Bode, AM
Carlson, J
Hunter, WS
Bronson, RT
机构
[1] So Illinois Univ, Sch Med, Dept Physiol, Carbondale, IL 62901 USA
[2] Univ N Dakota, Sch Med, Dept Physiol, Grand Forks, ND 58202 USA
[3] Edwin James Res Ctr, Grand Forks, ND 58202 USA
[4] Univ Waterloo, Dept Biol, Waterloo, ON N2L 3G1, Canada
[5] Tufts Univ, USDA, Human Nutr Res Ctr Aging, Boston, MA 02111 USA
关键词
growth hormone; dwarf mice; transgenic mice; body temperature; oxidative damage; tumors;
D O I
10.1016/S0531-5565(98)00032-1
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
It is very well documented that plasma growth hormone (GH) levels decline with age in the human and in experimental animals, and there is considerable evidence that age-related changes in body composition may be caused by reduced function of the GH-ICF-I system. However, excessive GH levels are associated with reduced life expectancy in acromegalic patients and with symptoms of accelerated aging in GH transgenic mice. Hereditary dwarf mice deficient in GH, prolactin, and TSH live much longer than their normal siblings. Possible mechanisms of delayed aging in dwarf mice include lower core body temperature and reduced oxidative processes. It is suggested that the controversies concerning the apparent potential of GH to both prevent and accelerate aging may be reconciled by interpreting the results in light of the negative relationship between body size and life span within a species. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:675 / 687
页数:13
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