How longevity research can lead to therapies for Alzheimer's disease: The rapamycin story

Arlan Richardson, Veronica Galvan, Ai Ling Lin, Salvatore Oddo

Research output: Contribution to journalArticlepeer-review

99 Scopus citations

Abstract

The discovery that rapamycin increases lifespan in mice and restores/delays many aging phenotypes has led to the speculation that rapamycin has 'anti-aging' properties. The major question discussed in this review is whether a manipulation that has anti-aging properties can alter the onset and/or progression of Alzheimer's disease, a disease in which age is the major risk factor. Rapamycin has been shown to prevent (and possibly restore in some cases) the deficit in memory observed in the mouse model of Alzheimer's disease (AD-Tg) as well as reduce Aβ and tau aggregation, restore cerebral blood flow and vascularization, and reduce microglia activation. All of these parameters are widely recognized as symptoms central to the development of AD. Furthermore, rapamycin has also been shown to improve memory and reduce anxiety and depression in several other mouse models that show cognitive deficits as well as in 'normal' mice. The current research shows the feasibility of using pharmacological agents that increase lifespan, such as those identified by the National Institute on Aging Intervention Testing Program, to treat Alzheimer's disease.

Original languageEnglish
Pages (from-to)51-58
Number of pages8
JournalExperimental Gerontology
Volume68
DOIs
StatePublished - Aug 1 2015

Bibliographical note

Publisher Copyright:
© 2014.

Funding

This work was supported in part by a RC2AG036613 NIH Recovery Act Great Opportunities grant.

FundersFunder number
NIH Recovery
National Institutes of Health (NIH)R01AG037637
National Institute on AgingRC2AG036613

    Keywords

    • Alzheimer's disease
    • Behavior
    • Cognition
    • Rapamycin

    ASJC Scopus subject areas

    • Biochemistry
    • Aging
    • Molecular Biology
    • Genetics
    • Endocrinology
    • Cell Biology

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