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生长激素与衰老:新发现

Growth Hormone and Aging: New Findings.

作者信息

Bartke Andrzej, Hascup Erin, Hascup Kevin, Masternak Michal M

机构信息

Department of Internal Medicine, Southern Illinois University School of Medicine, Springfield, IL, USA.

Department of Neurology, Southern Illinois University School of Medicine, Springfield, IL, USA.

出版信息

World J Mens Health. 2021 Jul;39(3):454-465. doi: 10.5534/wjmh.200201. Epub 2021 Feb 3.

Abstract

Complex relationships between growth hormone (GH) signaling and mammalian aging continue to attract attention of many investigators. Recent results include evidence that the impact of GH on genome maintenance (DNA damage and repair) is drastically different in normal as compared to cancer cells, consistent with GH promoting aging and cancer progression. Impact of GH on DNA methylation was studied as a possible mechanism linking actions of GH during early life to the trajectory of aging. Animals with reduced or enhanced GH signaling and novel animals with adipocyte-specific deletion of GH receptors were used to elucidate the effects of GH on white and brown adipose tissue, including the impact of this hormone on lipolysis, fibrosis, and thermogenesis. Effects of GH on adipose tissue related to lipid and energy metabolism emerge as mechanistic links between GH, healthspan, and lifespan. Treatment of healthy men with a combination of GH, dehydroepiandrosterone, and metformin was reported to restore thymus function and reduce epigenetic age. Studies of human subjects with deficiency of GH or GH receptors and studies of mice with the same endocrine syndromes identified several phenotypic changes related (positively or negatively) to the previously reported predisposition to healthy aging. Results of these and other recent studies advance present understanding of the mechanisms by which GH influences aging and longevity and of the trade-offs involved.

摘要

生长激素(GH)信号传导与哺乳动物衰老之间的复杂关系持续吸引着众多研究者的关注。近期研究结果表明,与癌细胞相比,GH对基因组维持(DNA损伤与修复)的影响在正常细胞中截然不同,这与GH促进衰老和癌症进展的观点相符。对GH对DNA甲基化的影响进行了研究,这可能是一种将GH在生命早期的作用与衰老轨迹联系起来的机制。利用GH信号传导减弱或增强的动物以及新型的脂肪细胞特异性GH受体缺失动物,来阐明GH对白色和棕色脂肪组织的影响,包括该激素对脂肪分解、纤维化和产热的影响。GH对与脂质和能量代谢相关的脂肪组织的影响,成为了GH、健康寿命和寿命之间的机制性联系。据报道,用GH、脱氢表雄酮和二甲双胍联合治疗健康男性可恢复胸腺功能并降低表观遗传年龄。对GH或GH受体缺乏的人类受试者的研究以及对具有相同内分泌综合征的小鼠的研究,确定了一些与先前报道的健康衰老易感性相关(正向或负向)的表型变化。这些及其他近期研究的结果推动了目前对GH影响衰老和长寿的机制以及其中权衡关系的理解。

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