Ruby Chrisp
Sex-specific attenuation of constant light-induced memory impairment and Clock gene expression in brain in hepatic Npas2 knockout mice
Chrisp, Ruby; Masterson, Mitchell; Pope, Rebecca; Roberts, Christopher J.; Collins, Hilary M.; Watson, David J.G.; O’Neil, Derek; Aagaard, Kjersti M.; Gibson, Claire L.; Heery, David M.; Moran, Paula M.
Authors
Mitchell Masterson
Rebecca Pope
Mr CHRISTOPHER ROBERTS Christopher.Roberts2@nottingham.ac.uk
Research Fellow
Dr HILARY COLLINS HILARY.COLLINS@NOTTINGHAM.AC.UK
SCIENTIFIC OFFICER
David J.G. Watson
Derek O’Neil
Kjersti M. Aagaard
Professor CLAIRE GIBSON Claire.Gibson@nottingham.ac.uk
Head of School (Professor of Psychology)
Professor DAVID HEERY david.heery@nottingham.ac.uk
PROFESSOR OF EUCARYOTIC GENE REGULATION
Paula M. Moran
Abstract
NPAS2 (Neuronal PAS Domain Protein 2) is a component of the core circadian clock and the coordinated activity between central brain and peripheral liver clock proteins postulated to be instrumental for linking behaviour and metabolism. We investigated a conditional liver-specific knockout mouse model (Npas2-/- or cKO) to explore its function in activity, circadian rhythms and cognition (novel object recognition-NOR). Circadian rhythms showed no genotype differences. Constant-light reduced NOR in floxxed controls but remarkably not in Npas2-/- mice, particularly females. Consistent with entrainment of systemic and central circadian biology, Npas2-/- mice showed altered expression of circadian gene Clock in frontal cortex. Sex differences independent of genotype were found in expression of circadian genes Clock, Bmal1 and Reverb-b in brain. Sex differences in Clock were absent in Npas2-/- mice. Females showed greater period length and phase response to constant light independently of genotype. The data suggest that a role for peripheral NPAS2 in constant light-induced memory impairment in females, and potential mediation by altered cortical circadian Clock gene expression, merit further investigation. These findings have implications for the interaction between peripheral and central circadian clocks, circadian sex differences and the deleterious effects of constant light on cognition.
Citation
Chrisp, R., Masterson, M., Pope, R., Roberts, C. J., Collins, H. M., Watson, D. J., O’Neil, D., Aagaard, K. M., Gibson, C. L., Heery, D. M., & Moran, P. M. (2025). Sex-specific attenuation of constant light-induced memory impairment and Clock gene expression in brain in hepatic Npas2 knockout mice. Scientific Reports, 15(1), Article 8347. https://doi.org/10.1038/s41598-025-92938-1
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 4, 2025 |
Online Publication Date | Mar 11, 2025 |
Publication Date | Mar 11, 2025 |
Deposit Date | Mar 10, 2025 |
Publicly Available Date | Sep 12, 2025 |
Journal | Scientific Reports |
Electronic ISSN | 2045-2322 |
Publisher | Nature Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 15 |
Issue | 1 |
Article Number | 8347 |
DOI | https://doi.org/10.1038/s41598-025-92938-1 |
Public URL | https://nottingham-repository.worktribe.com/output/46189607 |
Publisher URL | https://www.nature.com/articles/s41598-025-92938-1 |
Additional Information | Received: 21 August 2024; Accepted: 4 March 2025; First Online: 11 March 2025; : ; : The authors declare no competing interests. |
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Sex-specific attenuation of constant light-induced memory impairment and Clock gene expression in brain in Hepatic Npas2 knockout mice
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