Barron Anna M, Pike Christian J
USC Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089 USA.
Front Biosci (Elite Ed). 2012 Jan 1;4(3):976-97. doi: 10.2741/E434.
A promising strategy to delay and perhaps prevent Alzheimer's disease (AD) is to identify the age-related changes that put the brain at risk for the disease. A significant normal age change known to result in tissue-specific dysfunction is the depletion of sex hormones. In women, menopause results in a relatively rapid loss of estradiol and progesterone. In men, aging is associated with a comparatively gradual yet significant decrease in testosterone. We review a broad literature that indicates age-related losses of estrogens in women and testosterone in men are risk factors for AD. Both estrogens and androgens exert a wide range of protective actions that improve multiple aspects of neural health, suggesting that hormone therapies have the potential to combat AD pathogenesis. However, translation of experimental findings into effective therapies has proven challenging. One emerging treatment option is the development of novel hormone mimetics termed selective estrogen and androgen receptor modulators. Continued research of sex hormones and their roles in the aging brain is expected to yield valuable approaches to reducing the risk of AD.
一种延缓甚至可能预防阿尔茨海默病(AD)的有前景的策略是识别那些使大脑面临该疾病风险的与年龄相关的变化。已知会导致组织特异性功能障碍的一个显著的正常年龄变化是性激素的耗竭。在女性中,更年期导致雌二醇和孕酮相对快速流失。在男性中,衰老与睾酮相对逐渐但显著的减少有关。我们综述了广泛的文献,这些文献表明女性雌激素和男性睾酮与年龄相关的流失是AD的风险因素。雌激素和雄激素都发挥着广泛的保护作用,可改善神经健康的多个方面,这表明激素疗法有可能对抗AD的发病机制。然而,将实验结果转化为有效疗法已被证明具有挑战性。一种新兴的治疗选择是开发新型激素模拟物,即选择性雌激素和雄激素受体调节剂。对性激素及其在衰老大脑中的作用的持续研究有望产生降低AD风险的有价值方法。