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脱氢表雄酮与衰老相关疾病

Dehydroepiandrosterone and diseases of aging.

作者信息

Watson R R, Huls A, Araghinikuam M, Chung S

机构信息

Arizona Prevention Center, University of Arizona, School of Medicine, Tucson, USA.

出版信息

Drugs Aging. 1996 Oct;9(4):274-91. doi: 10.2165/00002512-199609040-00005.

Abstract

Dehydroepiandrosterone (DHEA; prasterone) is a major adrenal hormone with no well accepted function. In both animals and humans, low DHEA levels occur with the development of a number of the problems of aging: immunosenesence, increased mortality, increased incidence of several cancers, loss of sleep, decreased feelings of well-being, osteoporosis and atherosclerosis. DHEA replacement in aged mice significantly normalised immunosenescence, suggesting that this hormone plays a key role in aging and immune regulation in mice. Similarly, osteoclasts and lymphoid cells were stimulated by DHEA replacement, an effect that may delay osteoporosis. Recent studies do not support the original suggestion that low serum DHEA levels are associated with Alzheimer's disease and other forms of cognitive dysfunction in the elderly. As DHEA modulates energy metabolism, low levels should affect lipogenesis and gluconeogenesis, increasing the risk of diabetes mellitus and heart disease. Most of the effects of DHEA replacement have been extrapolated from epidemiological or animal model studies, and need to be tested in human trials. Studies that have been conducted in humans show essentially no toxicity of DHEA treatment at dosages that restore serum levels, with evidence of normalisation in some aging physiological systems. Thus, DHEA deficiency may expedite the development of some diseases that are common in the elderly.

摘要

脱氢表雄酮(DHEA;普拉睾酮)是一种主要的肾上腺激素,其功能尚未得到广泛认可。在动物和人类中,随着多种衰老问题的出现,脱氢表雄酮水平会降低,这些问题包括免疫衰老、死亡率增加、多种癌症发病率上升、睡眠障碍、幸福感下降、骨质疏松和动脉粥样硬化。给老年小鼠补充脱氢表雄酮可显著使免疫衰老正常化,这表明这种激素在小鼠的衰老和免疫调节中起关键作用。同样地,补充脱氢表雄酮可刺激破骨细胞和淋巴细胞,这种作用可能会延缓骨质疏松。最近的研究并不支持最初的观点,即血清脱氢表雄酮水平低与老年人的阿尔茨海默病及其他形式的认知功能障碍有关。由于脱氢表雄酮可调节能量代谢,其水平低会影响脂肪生成和糖异生,增加患糖尿病和心脏病的风险。大多数补充脱氢表雄酮的效果是从流行病学或动物模型研究中推断出来的,需要在人体试验中进行验证。在人体中进行的研究表明,在恢复血清水平的剂量下,脱氢表雄酮治疗基本没有毒性,并且在一些衰老生理系统中有正常化的证据。因此,脱氢表雄酮缺乏可能会加速老年人常见的一些疾病的发展。

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