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脱氢表雄酮/硫酸脱氢表雄酮在冠心病中起保护作用吗?

Do DHEA/DHEAS play a protective role in coronary heart disease?

作者信息

Porsová-Dutoit I, Sulcová J, Stárka L

机构信息

Department of Internal Medicine, Groupe Hospitalier Pitie-Salpetriere, Paris, France.

出版信息

Physiol Res. 2000;49 Suppl 1:S43-56.

Abstract

Dehydroepiandrosterone (DHEA) and dehydroepiandrosterone-sulfate (DHEAS), the major androgens secreted by human adrenal glands, were suggested to play a protective role in the pathogenesis of atherosclerosis and coronary heart disease. On the basis of a critical review of all existing studies we concluded that 1) there is no evidence of a protective role of DHEA and DHEAS in women, and 2) men with low plasma DHEA and DHEAS levels can be considered as beings at risk of developing a fatal cardiovascular event. These androgens can interfere with atherogenic process by several mechanisms. They influence enzymes such as glucoso-6-phosphate dehydrogenase, which can modify the lipid spectrum. Furthermore, they can inhibit human platelet aggregation, enhance fibrinolysis, slow down cell proliferation and reduce plasma levels of plasminogen activator inhibitor type 1 and tissue plasminogen activator antigen. We suggest that all these DHEA(S) actions are dependent on sex hormone metabolic pathways. There are still insufficient data to advise DHEA supplementation in elderly men, but this type of hormone replacement therapy merits further studies.

摘要

脱氢表雄酮(DHEA)和硫酸脱氢表雄酮(DHEAS)是人体肾上腺分泌的主要雄激素,有人认为它们在动脉粥样硬化和冠心病的发病机制中起保护作用。在对所有现有研究进行批判性综述的基础上,我们得出以下结论:1)没有证据表明DHEA和DHEAS对女性有保护作用;2)血浆DHEA和DHEAS水平低的男性可被视为有发生致命心血管事件风险的人群。这些雄激素可通过多种机制干扰动脉粥样硬化进程。它们会影响葡萄糖-6-磷酸脱氢酶等酶,而这些酶可改变血脂谱。此外,它们能抑制人体血小板聚集、增强纤维蛋白溶解、减缓细胞增殖并降低血浆中1型纤溶酶原激活物抑制剂和组织纤溶酶原激活物抗原的水平。我们认为所有这些DHEA(S)的作用都依赖于性激素代谢途径。目前仍缺乏足够的数据来建议老年男性补充DHEA,但这种激素替代疗法值得进一步研究。

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