Hodgin Jeffrey B, Maeda Nobuyo
Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina 27599-7525, USA.
Endocrinology. 2002 Dec;143(12):4495-501. doi: 10.1210/en.2002-220844.
The use of hormone replacement therapy for coronary heart disease prevention in humans has been an area of intense controversy. The atheroprotective qualities of estrogens have been challenged recently by several negative results of randomized clinical trials in postmenopausal women. However, the inhibitory effects of estrogens on atherogenesis are well documented in numerous animals, including atherosclerotic mouse models, but the detailed mechanisms of this protection are not understood. In this minireview, we will focus on the considerable success that has been achieved in demonstrating the atheroprotective effects of 17beta-estradiol in apolipoprotein E and low-density lipoprotein receptor-deficient mice and the use of these atherosclerotic mouse models in pharmacological and genetic study designs to investigate antiatherogenic mechanisms of estrogens. Mouse models of atherosclerosis should prove beneficial to understanding the cellular and molecular mechanisms of estrogen-mediated atheroprotection and aid the development of improved therapies to confer the benefits and reduce the risks associated with hormone replacement therapy.
在人类中使用激素替代疗法预防冠心病一直是一个备受争议的领域。最近,绝经后妇女的几项随机临床试验的负面结果对雌激素的抗动脉粥样硬化特性提出了挑战。然而,雌激素对动脉粥样硬化形成的抑制作用在包括动脉粥样硬化小鼠模型在内的众多动物中已有充分记录,但这种保护作用的详细机制尚不清楚。在这篇小型综述中,我们将重点关注在证明17β-雌二醇对载脂蛋白E和低密度脂蛋白受体缺陷小鼠的抗动脉粥样硬化作用方面所取得的显著成功,以及在药理学和遗传学研究设计中使用这些动脉粥样硬化小鼠模型来研究雌激素的抗动脉粥样硬化机制。动脉粥样硬化小鼠模型应有助于理解雌激素介导的抗动脉粥样硬化保护作用的细胞和分子机制,并有助于开发更好的疗法,以赋予激素替代疗法的益处并降低其相关风险。