Bartke A, Brown-Borg H M, Bode A M, Carlson J, Hunter W S, Bronson R T
Department of Physiology, Southern Illinois University School of Medicine, Carbondale 62901-6512, USA.
Exp Gerontol. 1998 Nov-Dec;33(7-8):675-87. doi: 10.1016/s0531-5565(98)00032-1.
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-IGF-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.
有充分的文献记载,在人类和实验动物中,血浆生长激素(GH)水平会随着年龄的增长而下降,并且有大量证据表明,GH-IGF-I系统功能的降低可能导致与年龄相关的身体成分变化。然而,肢端肥大症患者的GH水平过高与预期寿命缩短有关,而在GH转基因小鼠中则出现加速衰老的症状。缺乏GH、催乳素和促甲状腺激素的遗传性侏儒小鼠比它们的正常同胞寿命长得多。侏儒小鼠延缓衰老的可能机制包括较低的核心体温和减少的氧化过程。有人提出,关于GH明显具有预防和加速衰老双重潜力的争议,可能通过根据物种内体型与寿命之间的负相关关系来解释结果而得到调和。