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Updated: Oct 9, 2025

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Published on: November 6, 2017
TOR-dependent cerebrovascular aging in Alzheimer's disease
Jordan B Jahrling1, Veronica Galvan1,2
1Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX 78245, USA.
Aging vascular dysfunction contributes to neurological diseases. Attenuating mammalian/mechanistic target of rapamycin (mTOR) extends lifespan and delays aging, suggesting mTOR
Area of Science:
- Gerontology and Neuroscience
- Vascular Biology
- Molecular Medicine
Background:
- Vascular dysfunction is a hallmark of aging and linked to neurological diseases.
- Mammalian/mechanistic target of rapamycin (mTOR) inhibition extends lifespan and healthspan in mice.
- Understanding aging mechanisms is crucial for treating age-related cognitive decline.
Purpose of the Study:
- To review evidence linking mTOR to age-associated vascular dysfunction.
- To explore mTOR's role in cognitive decline, particularly in Alzheimer's disease.
- To discuss potential therapeutic strategies targeting mTOR.
Main Methods:
- Literature review of existing studies on mTOR, vascular aging, and neurological diseases.
- Analysis of proposed molecular mechanisms.
- Synthesis of current evidence and identification of research gaps.
Main Results:
- mTOR pathway plays a critical role in age-related vascular dysfunction.
- Evidence suggests mTOR contributes to the pathogenesis of Alzheimer's disease.
- mTOR inhibition shows promise in mitigating aging-related vascular and cognitive decline.
Conclusions:
- Targeting the mTOR pathway may offer a novel therapeutic approach for age-related neurological disorders.
- Further research is needed to elucidate the precise mechanisms linking mTOR, vascular health, and cognitive function.
- Interventions aimed at modulating mTOR could potentially improve brain health during aging.
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