Circadian regulation of hippocampal function is disrupted with corticosteroid treatment

Matthew T Birnie*, Matthew D B Claydon, Oliver R Troy, Becky L Conway-Campbell

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

19 Citations (Scopus)

Abstract

Disrupted circadian activity is associated with many neuropsychiatric disorders. A major coordinator of circadian biological systems is adrenal glucocorticoid secretion which exhibits a pronounced preawakening peak that regulates metabolic, immune, and cardiovascular processes, as well as mood and cognitive function. Loss of this circadian rhythm during corticosteroid therapy is often associated with memory impairment. Surprisingly, the mechanisms that underlie this deficit are not understood. In this study, in rats, we report that circadian regulation of the hippocampal transcriptome integrates crucial functional networks that link corticosteroid-inducible gene regulation to synaptic plasticity processes via an intrahippocampal circadian transcriptional clock. Further, these circadian hippocampal functions were significantly impacted by corticosteroid treatment delivered in a 5-d oral dosing treatment protocol. Rhythmic expression of the hippocampal transcriptome, as well as the circadian regulation of synaptic plasticity, was misaligned with the natural light/dark circadian-entraining cues, resulting in memory impairment in hippocampal-dependent behavior. These findings provide mechanistic insights into how the transcriptional clock machinery within the hippocampus is influenced by corticosteroid exposure, leading to adverse effects on critical hippocampal functions, as well as identifying a molecular basis for memory deficits in patients treated with long-acting synthetic corticosteroids.
Original languageEnglish
Article numbere2211996120
Number of pages11
JournalProceedings of the National Academy of Sciences
Volume120
Issue number15
Early online date6 Apr 2023
DOIs
Publication statusPublished - 11 Apr 2023

Bibliographical note

Funding Information:
ACKNOWLEDGMENTS. This research was funded by the Wellcome Trust 089647/Z/09/Z awarded to B.L.C-C., and S.L.L. and the United Kingdom Medical Research Council grant MR/R010919/1 supporting M.T.B., B.L.C-C., and S.L.L. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Publisher Copyright:
Copyright © 2023 the Author(s).

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