USC Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089, USA.
Horm Behav. 2013 Feb;63(2):301-7. doi: 10.1016/j.yhbeh.2012.04.006. Epub 2012 Apr 19.
Age-related loss of sex steroid hormones is a established risk factor for the development of Alzheimer's disease (AD) in women and men. While the relationships between the sex steroid hormones and AD are not fully understood, findings from both human and experimental paradigms indicate that depletion of estrogens in women and androgens in men increases vulnerability of the aging brain to AD pathogenesis. We review evidence of a wide range of beneficial neural actions of sex steroid hormones that may contribute to their hypothesized protective roles against AD. Both estrogens and androgens exert general neuroprotective actions relevant to a several neurodegenerative conditions, some in a sex-specific manner, including protection from neuron death and promotion of select aspects of neural plasticity. In addition, estrogens and androgens regulate key processes implicated in AD pathogenesis, in particular the accumulation of β-amyloid protein. We discuss evidence of hormone-specific mechanisms related to the regulation of the production and clearance of β-amyloid as critical protective pathways. Continued elucidation of these pathways promises to yield effective hormone-based strategies to delay development of AD.
随着年龄增长,性激素减少是导致女性和男性阿尔茨海默病(AD)的既定风险因素。尽管人们对性激素与 AD 之间的关系尚未完全了解,但来自人类和实验范例的研究结果表明,女性雌激素枯竭和男性雄激素枯竭会增加衰老大脑对 AD 发病机制的易感性。我们回顾了性激素具有广泛的有益神经作用的证据,这些作用可能有助于它们对 AD 的假设保护作用。雌激素和雄激素都具有与几种神经退行性疾病相关的一般神经保护作用,有些作用具有性别特异性,包括防止神经元死亡和促进神经可塑性的某些方面。此外,雌激素和雄激素调节 AD 发病机制中涉及的关键过程,特别是β-淀粉样蛋白的积累。我们讨论了与β-淀粉样蛋白的产生和清除有关的激素特异性机制的证据,这是关键的保护途径。对这些途径的进一步阐明有望产生有效的基于激素的策略来延迟 AD 的发展。