Pluchino N, Drakopoulos P, Bianchi-Demicheli F, Wenger J M, Petignat P, Genazzani A R
Division of Gynecology and Obstetrics, University Hospital of Geneva, Geneva, Switzerland.
Division of Gynecology and Obstetrics, University Hospital of Geneva, Geneva, Switzerland.
J Steroid Biochem Mol Biol. 2015 Jan;145:273-80. doi: 10.1016/j.jsbmb.2014.04.012. Epub 2014 Jun 2.
Dehydroepiandrosterone (DHEA) and its sulfate ester, DHEAS, are the most abundant steroid hormones in the humans. However, their physiological significance, their mechanisms of action and their possible roles as treatment are not fully clarified. Biological actions of DHEA(S) in the brain involve neuroprotection, neurite growth, neurogenesis and neuronal survival, apoptosis, catecholamine synthesis and secretion, as well as anti-oxidant, anti-inflammatory and antiglucocorticoid effects. In addition, DHEA affects neurosteroidogenis and endorphin synthesis/release. We also demonstrated in a model of ovariectomized rats that DHEA therapy increases proceptive behaviors, already after 1 week of treatment, affecting central function of sexual drive. In women, the analyses of clinical outcomes are far from being conclusive and many issues should still be addressed. Although DHEA preparations have been available in the market since the 1990s, there are very few definitive reports on the biological functions of this steroid. We demonstrate that 1 year DHEA administration at the dose of 10mg provided a significant improvement in comparison with vitamin D in sexual function and in frequency of sexual intercourse in early postmenopausal women. Among symptomatic women, the spectrum of symptoms responding to DHEA requires further investigation, to define the type of sexual symptoms (e.g. decreased sexual function or hypoactive sexual desire disorder) and the degree of mood/cognitive symptoms that could be responsive to hormonal treatment. In this regard, our findings are promising, although they need further exploration with a larger and more representative sample size. This article is part of a Special Issue entitled: Essential role of DHEA.
脱氢表雄酮(DHEA)及其硫酸酯(DHEAS)是人体内含量最为丰富的类固醇激素。然而,它们的生理意义、作用机制以及作为治疗手段的潜在作用尚未完全阐明。DHEA(S)在大脑中的生物学作用包括神经保护、神经突生长、神经发生、神经元存活、凋亡、儿茶酚胺合成与分泌,以及抗氧化、抗炎和抗糖皮质激素作用。此外,DHEA还会影响神经甾体生成和内啡肽的合成/释放。我们还在去卵巢大鼠模型中证明,DHEA治疗在治疗1周后就能增加接受性行为,影响性驱力的中枢功能。对于女性而言,临床结果分析远未得出定论,许多问题仍有待解决。尽管自20世纪90年代以来DHEA制剂就已投放市场,但关于这种类固醇生物学功能的确切报告却非常少。我们证明,与维生素D相比,对绝经后早期女性给予10mg剂量的DHEA进行为期1年的给药,能显著改善性功能和性交频率。在有症状的女性中,对DHEA有反应的症状范围需要进一步研究,以确定性症状的类型(如性功能减退或性兴趣减退障碍)以及可能对激素治疗有反应的情绪/认知症状的程度。在这方面,我们的研究结果很有前景,尽管需要用更大且更具代表性的样本量进行进一步探索。本文是名为:DHEA的重要作用的特刊的一部分。