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Pharmacological activation of Nr4a rescues age-associated memory decline

Research output: Contribution to journalArticle

Snehajyoti Chatterjee, Emily N. Walsh, Amy L. Yan, K. Peter Giese, Stephen Safe, Ted Abel

Original languageEnglish
Pages (from-to)140-144
Number of pages5
JournalNeurobiology of Aging
Volume85
DOIs
Publication statusPublished - 1 Jan 2020

King's Authors

Abstract

Age-associated cognitive impairments affect an individual's quality of life and are a growing problem in society. Therefore, therapeutic strategies to treat age-related cognitive decline are needed to enhance the quality of life among the elderly. Activation of the Nr4a family of transcription factors has been closely linked to memory formation and dysregulation of these transcription factors is thought to be associated with age-related cognitive decline. Previously, we have shown that Nr4a transcription can be activated by synthetic bisindole-derived compounds (C-DIM). C-DIM compounds enhance synaptic plasticity and long-term contextual fear memory in young healthy mice. In this study, we show that activation of Nr4a2 by 1,1-bis(3′-Indolyl)-1-(p-chlorophenyl) methane (C-DIM12), enhances long-term spatial memory in young mice and rescues memory deficits in aged mice. These findings suggest that C-DIM activators of Nr4a transcription may be suitable to prevent memory deficits associated with aging.

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