Department of Cellular and Integrative Physiology and The Barshop Institute for Longevity and Aging Studies, University of Texas Health San Antonio, San Antonio, TX, USA.
Gerontology. 2018;64(3):205-211. doi: 10.1159/000485381. Epub 2018 Jan 11.
Cerebrovascular dysfunction is detected prior to the onset of cognitive and histopathological changes in Alzheimer's disease (AD). Increasing evidence indicates a critical role of cerebrovascular dysfunction in the initiation and progression of AD. Recent studies identified the mechanistic/mammalian target of rapamycin (mTOR) as a critical effector of cerebrovascular dysfunction in AD. mTOR has a key role in the regulation of metabolism, but some mTOR-dependent mechanisms are uniquely specific to the regulation of cerebrovascular function. These include the regulation of cerebral blood flow, blood-brain barrier integrity and maintenance, neurovascular coupling, and cerebrovascular reactivity. This article examines the available evidence for a role of mTOR-driven cerebrovascular dysfunction in the pathogenesis of AD and of vascular cognitive impairment and dementia (VCID) and highlights the therapeutic potential of targeting mTOR and/or specific downstream effectors for vasculoprotection in AD, VCID, and other age-associated neurological diseases with cerebrovascular etiology.
脑血管功能障碍在阿尔茨海默病(AD)认知和组织病理学变化发生之前就已被检测到。越来越多的证据表明,脑血管功能障碍在 AD 的发生和发展中起着关键作用。最近的研究确定了机械/哺乳动物雷帕霉素靶蛋白(mTOR)作为 AD 中脑血管功能障碍的关键效应因子。mTOR 在代谢调节中起着关键作用,但一些 mTOR 依赖性机制是专门针对脑血管功能调节的。这些包括脑血流的调节、血脑屏障的完整性和维持、神经血管耦联以及脑血管反应性。本文探讨了 mTOR 驱动的脑血管功能障碍在 AD 发病机制以及血管性认知障碍和痴呆(VCID)中的作用的现有证据,并强调了针对 mTOR 和/或特定下游效应物进行血管保护治疗 AD、VCID 和其他具有脑血管病因的与年龄相关的神经退行性疾病的治疗潜力。