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A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain

Miranda E. Orr

Journal of Alzheimer s Disease · 2024 · ▲ 5 citations

Abstract

Cellular senescence(definition) contributes to Alzheimer's disease (AD) pathogenesis. Treatments that remove senescent cells, senolytics(definition), improve brain outcomes in AD mice with amyloid-β or tau deposition. 3xTgAD mice develop both AD neuropathologies; however, Ng et al. report low p16INK4a-associated senescence in the brain. Senolytic treatment by genetic removal; dasatinib with quercetin (D+Q), which enter the brain; and ABT-263 with limited brain penetrance all reduced AD neuropathology. Refined measures of senescence and brain exposure would help clarify the benefits of senolytics despite low p16INK4a-associated senescence and potential limited brain penetrance.

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Provenance

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OpenAlex
DOI
10.3233/jad-231462
Canonical
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Fetched
2026-06-15 MST

Cite this

APA
Orr, M.E. (2024). A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain. <em>Journal of Alzheimer s Disease</em>. https://doi.org/10.3233/jad-231462
Vancouver
Orr ME. A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain. Journal of Alzheimer s Disease. 2024. doi:10.3233/jad-231462.
BibTeX
@unpublished{miranda2024ANeedf, title = {A Need for Refined Senescence Biomarkers and Measures of Senolytics in the Brain}, author = {Miranda E. Orr}, journal = {Journal of Alzheimer s Disease}, year = {2024}, doi = {10.3233/jad-231462}, }

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