| Literature DB >> 29320772 |
Candice E Van Skike1, Veronica Galvan.
Abstract
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.Entities:
Keywords: Alzheimer’s disease; Blood-brain barrier; Cerebral blood flow; Neurovascular coupling; Rapamycin; Vascular density; mTOR
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Year: 2018 PMID: 29320772 PMCID: PMC5876078 DOI: 10.1159/000485381
Source DB: PubMed Journal: Gerontology ISSN: 0304-324X Impact factor: 5.140