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Small molecule cognitive enhancer reverses age-related memory decline in mice.

Karen Krukowski | Amber Nolan | Elma S Frias | Morgane Boone | Gonzalo Ureta | Katherine Grue | Maria-Serena Paladini | Edward Elizarraras | Luz Delgado | Sebastian Bernales | Peter Walter | Susanna Rosi
eLife | 2020

With increased life expectancy, age-associated cognitive decline becomes a growing concern, even in the absence of recognizable neurodegenerative disease. The integrated stress response (ISR) is activated during aging and contributes to age-related brain phenotypes. We demonstrate that treatment with the drug-like small-molecule ISR inhibitor ISRIB reverses ISR activation in the brain, as indicated by decreased levels of activating transcription factor 4 (ATF4) and phosphorylated eukaryotic translation initiation factor eIF2. Furthermore, ISRIB treatment reverses spatial memory deficits and ameliorates working memory in old mice. At the cellular level in the hippocampus, ISR inhibition (i) rescues intrinsic neuronal electrophysiological properties, (ii) restores spine density and (iii) reduces immune profiles, specifically interferon and T cell-mediated responses. Thus, pharmacological interference with the ISR emerges as a promising intervention strategy for combating age-related cognitive decline in otherwise healthy individuals.

Pubmed ID: 33258451

Research resources used in this publication

None found

Antibodies used in this publication

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Associated grants

  • Agency: NIA NIH HHS, United States
    Id: R01 AG056770
  • Agency: NCATS NIH HHS, United States
    Id: TL1 TR001871
  • Agency: Programa de Apoyo a Centros con Financiamiento Basal, International
    Id: AFB 170004
  • Agency: NIGMS NIH HHS, United States
    Id: R25 GM056847
  • Agency: NIA NIH HHS, United States
    Id: F32 AG054126
  • Agency: NINDS NIH HHS, United States
    Id: K08 NS114170

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PRISM (tool)

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