Department of Pharmacy, Southeast University, Dhaka, Bangladesh.
Pharmakon Neuroscience Research Network, Dhaka, Bangladesh.
Mol Neurobiol. 2020 Jun;57(6):2654-2670. doi: 10.1007/s12035-020-01911-8. Epub 2020 Apr 15.
Estrogens play a crucial physiological function in the brain; however, debates exist concerning the role of estrogens in Alzheimer's disease (AD). Women during pre-, peri-, or menopause periods are more susceptible for developing AD, suggesting the connection of sex factors and a decreased estrogen signaling in AD pathogenesis. Yet, the underlying mechanism of estrogen-mediated neuroprotection is unclarified and is complicated by the existence of estrogen-related factors. Consequently, a deeper analysis of estrogen receptor (ER) expression and estrogen-metabolizing enzymes could interpret the importance of estrogen in age-linked cognitive alterations. Previous studies propose that hormone replacement therapy may attenuate AD onset in postmenopausal women, demonstrating that estrogen signaling is important for the development and progression of AD. For example, ERα exerts neuroprotection against AD by maintaining intracellular signaling cascades and study reported reduced expression of ERα in hippocampal neurons of AD patients. Similarly, reduced expression of ERβ in female AD patients has been associated with abnormal function in mitochondria and improved markers of oxidative stress. In this review, we discuss the critical interaction between estrogen signaling and AD. Moreover, we highlight the potential of targeting estrogen-related signaling for therapeutic intervention in AD.
雌激素在大脑中起着至关重要的生理功能;然而,关于雌激素在阿尔茨海默病(AD)中的作用存在争议。处于绝经前、围绝经期或绝经后期间的女性更容易患上 AD,这表明性别因素和 AD 发病机制中雌激素信号的降低有关。然而,雌激素介导的神经保护的潜在机制尚不清楚,并且存在与雌激素相关的因素使情况变得复杂。因此,对雌激素受体(ER)表达和雌激素代谢酶的更深入分析可以解释雌激素在与年龄相关的认知改变中的重要性。先前的研究表明,激素替代疗法可能会减轻绝经后妇女的 AD 发病,这表明雌激素信号对 AD 的发展和进展很重要。例如,ERα 通过维持细胞内信号级联反应来发挥对 AD 的神经保护作用,研究报告称 AD 患者海马神经元中的 ERα 表达减少。同样,女性 AD 患者中 ERβ 的表达减少与线粒体功能异常和氧化应激标志物改善有关。在这篇综述中,我们讨论了雌激素信号与 AD 之间的关键相互作用。此外,我们强调了针对雌激素相关信号进行治疗干预 AD 的潜力。