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脱氢表雄酮(DHEA)作用的新机制。

Novel mechanisms for DHEA action.

作者信息

Prough Russell A, Clark Barbara J, Klinge Carolyn M

机构信息

Department of Biochemistry and Molecular GeneticsCenter for Genetics and Molecular Medicine, University of Louisville School of Medicine, Louisville, KY, USA.

Department of Biochemistry and Molecular GeneticsCenter for Genetics and Molecular Medicine, University of Louisville School of Medicine, Louisville, KY, USA

出版信息

J Mol Endocrinol. 2016 Apr;56(3):R139-55. doi: 10.1530/JME-16-0013. Epub 2016 Feb 23.

Abstract

Dehydroepiandrosterone (3β-hydroxy-5-androsten-17-one, DHEA), secreted by the adrenal cortex, gastrointestinal tract, gonads, and brain, and its sulfated metabolite DHEA-S are the most abundant endogeneous circulating steroid hormones. DHEA actions are classically associated with age-related changes in cardiovascular tissues, female fertility, metabolism, and neuronal/CNS functions. Early work on DHEA action focused on the metabolism to more potent sex hormones, testosterone and estradiol, and the subsequent effect on the activation of the androgen and estrogen steroid receptors. However, it is now clear that DHEA and DHEA-S act directly as ligands for many hepatic nuclear receptors and G-protein-coupled receptors. In addition, it can function to mediate acute cell signaling pathways. This review summarizes the molecular mechanisms by which DHEA acts in cells and animal models with a focus on the 'novel' and physiological modes of DHEA action.

摘要

脱氢表雄酮(3β-羟基-5-雄烯-17-酮,DHEA)由肾上腺皮质、胃肠道、性腺和大脑分泌,其硫酸化代谢产物硫酸脱氢表雄酮(DHEA-S)是循环中最丰富的内源性甾体激素。DHEA的作用传统上与心血管组织、女性生育能力、新陈代谢以及神经元/中枢神经系统功能的年龄相关变化有关。早期关于DHEA作用的研究集中在其代谢为活性更强的性激素睾酮和雌二醇,以及随后对雄激素和雌激素甾体受体激活的影响。然而,现在已经明确,DHEA和DHEA-S可直接作为许多肝细胞核受体和G蛋白偶联受体的配体。此外,它还可介导急性细胞信号通路。本综述总结了DHEA在细胞和动物模型中的作用分子机制,重点关注DHEA作用的“新”生理模式。

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