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Systemic GLP-1R agonist treatment reverses mouse glial and neurovascular cell transcriptomic aging signatures in a genome-wide manner.

Commun Biol · 2021

Last updated 2026-05-28

In a mouse study, researchers found that a GLP-1 receptor agonist (a type of drug) reversed signs of brain aging at the genetic level across multiple brain cell types, including glial and vascular cells. The treatment also reduced genetic markers linked to Alzheimer’s disease that appear with aging. The findings suggest that GLP-1 drugs may help counteract brain aging and related diseases.

AI summary of the abstract below.

JournalCommun Biol, 2021
Citations30
Relative citation ratio1.66
NIH percentile68
Molecules
Conditions studied Alzheimers, Parkinsons

Abstract

Pharmacological reversal of brain aging is a long-sought yet challenging strategy for the prevention and treatment of age-related neurodegeneration, due to the diverse cell types and complex cellular pathways impacted by the aging process. Here, we report the genome-wide reversal of transcriptomic aging signatures in multiple major brain cell types, including glial and mural cells, by systemic glucagon-like peptide-1 receptor (GLP-1R) agonist (GLP-1RA) treatment. The age-related expression changes reversed by GLP-1RA encompass both shared and cell type-specific functional pathways that are implicated in aging and neurodegeneration. Concomitantly, Alzheimer's disease (AD)-associated transcriptomic signature in microglia that arises from aging is reduced. These results show the feasibility of reversing brain aging by pharmacological means, provide mechanistic insights into the neurological benefits of GLP-1RAs, and imply that GLP-1R agonism may be a generally applicable pharmacological intervention for patients at risk of age-related neurodegeneration.

Verbatim abstract via PubMed 34079050 ↗