Bartke A
Department of Physiology, Southern Illinois University School of Medicine, Carbondale 62901, USA.
Endocrine. 1998 Apr;8(2):103-8. doi: 10.1385/ENDO:8:2:103.
Although age-related decline in plasma growth hormone (GH) levels is well documented, the possible role of GH in the control of aging is controversial. Overexpression of GH in transgenic mice is associated with reduced life expectancy and numerous symptoms of premature aging. Ames dwarf mice with hereditary GH, prolactin, and thyrotropin deficiency live much longer than their normal siblings. In contrast to these indications that GH may accelerate aging, some physiological changes in the elderly resemble symptoms of GH deficiency and can be corrected by GH replacement. It is suggested that these seemingly contradictory observations are related to the dose-response characteristics of GH action, and to negative correlation between body size and life expectancy within a species. Physiological mechanisms linking plasma GH levels and body size with aging remain to be identified.
虽然血浆生长激素(GH)水平随年龄增长而下降已有充分记录,但GH在衰老控制中的可能作用仍存在争议。转基因小鼠中GH的过度表达与预期寿命缩短和许多早衰症状相关。患有遗传性GH、催乳素和促甲状腺激素缺乏的艾姆斯侏儒小鼠比其正常同胞寿命长得多。与这些表明GH可能加速衰老的迹象相反,老年人的一些生理变化类似于GH缺乏的症状,并且可以通过GH替代来纠正。有人认为,这些看似矛盾的观察结果与GH作用的剂量反应特性以及物种内体型与预期寿命之间的负相关有关。将血浆GH水平和体型与衰老联系起来的生理机制仍有待确定。