性激素对骨代谢的调节。

Regulation of Bone Metabolism by Sex Steroids.

机构信息

Robert and Arlene Kogod Center on Aging and Endocrine Research Unit, Mayo Clinic College of Medicine, Rochester, Minnesota 55905.

出版信息

Cold Spring Harb Perspect Med. 2018 Jan 2;8(1):a031211. doi: 10.1101/cshperspect.a031211.

Abstract

Osteoporosis is a significant public health problem, and a major cause of the disease is estrogen deficiency following menopause in women. In addition, considerable evidence now shows that estrogen is also a major regulator of bone metabolism in men. Since the original description of the effects of estrogen deficiency on bone by Fuller Albright more than 70 years ago, there has been enormous progress in understanding the mechanisms of estrogen and testosterone action on bone using human and mouse models. Although we understand more about the effects of estrogen on bone as compared with testosterone, both sex steroids do play important roles, perhaps in a somewhat compartment-specific (i.e., cancellous vs. cortical bone) manner. This review summarizes our current knowledge of sex steroid action on bone based on human and mouse studies, identifies both agreements and potential discrepancies between these studies, and suggests directions for future research in this important area.

摘要

骨质疏松症是一个重大的公共卫生问题,而女性绝经后雌激素缺乏是导致该病的主要原因。此外,大量证据表明,雌激素也是男性骨骼代谢的主要调节剂。自 70 多年前 Fuller Albright 最初描述雌激素缺乏对骨骼的影响以来,利用人类和小鼠模型,人们在理解雌激素和睾酮对骨骼作用的机制方面取得了巨大进展。尽管我们对雌激素对骨骼的作用的了解比对睾酮的了解要多,但这两种性激素都起着重要作用,也许是以一种特定部位(即松质骨与皮质骨)的方式。这篇综述总结了我们基于人类和小鼠研究对性激素对骨骼作用的现有认识,确定了这些研究之间的一致性和潜在差异,并为这一重要领域的未来研究提出了方向。

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