Brown-Borg Holly M
Department of Pharmacology, Physiology & Therapeutics, University of North Dakota School of Medicine & Health Sciences, 501 North Columbia Road, Grand Forks, ND 58203, United States.
Mol Cell Endocrinol. 2009 Feb 5;299(1):64-71. doi: 10.1016/j.mce.2008.07.001. Epub 2008 Jul 11.
There is a growing body of literature focusing on the somatotropic axis and regulation of aging and 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 wild-type animals with normal plasma hormone concentrations. This information, along with that found in multiple other species, implicates this anabolic pathway as the major regulator of longevity in animals.
越来越多的文献聚焦于生长激素轴以及衰老和长寿的调节。这些报告中的许多数据来自多种内分泌突变体,即那些生长激素(GH)和胰岛素样生长因子I(IGF-1)水平均升高或其中一种或两种激素缺乏的突变体。一般来说,自发的和基因工程导致的GH和IGF-1缺乏都会导致体型变小、性成熟发育延迟、与年龄相关的病理变化以及寿命延长。相比之下,与血浆激素浓度正常的野生型动物相比,循环GH水平高的特征包括体型较大、青春期提前和生殖衰老、癌症发病率增加以及寿命缩短。这些信息,连同在其他多个物种中发现的信息,表明这条合成代谢途径是动物长寿的主要调节因子。