# Sex-specific attenuation of constant light-induced memory impairment and Clock gene expression in brain in hepatic Npas2 knockout mice

**Authors:** Ruby Chrisp, Mitchell Masterson, Rebecca Pope, Christopher J. Roberts, Hilary M. Collins, David J. G. Watson, Derek O’Neil, Kjersti M. Aagaard, Claire L. Gibson, David M. Heery, Paula M. Moran

PMC · DOI: 10.1038/s41598-025-92938-1 · 2025-03-11

## TL;DR

Removing the Npas2 gene in mice livers affects memory under constant light, especially in females, and changes brain circadian gene expression.

## Contribution

This study reveals sex-specific effects of liver Npas2 deletion on memory and brain circadian gene expression under constant light.

## Key findings

- Npas2-/- mice showed resistance to constant light-induced memory impairment, especially in females.
- Npas2-/- mice exhibited altered Clock gene expression in the frontal cortex.
- Sex differences in circadian gene expression were absent in Npas2-/- mice.

## 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.

The online version contains supplementary material available at 10.1038/s41598-025-92938-1.

## Linked entities

- **Genes:** NPAS2 (neuronal PAS domain protein 2) [NCBI Gene 4862], CLOCK (clock circadian regulator) [NCBI Gene 9575], BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406], NR1D2 (nuclear receptor subfamily 1 group D member 2) [NCBI Gene 9975]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Npas2 (neuronal PAS domain protein 2) [NCBI Gene 18143] {aka MOP4, bHLHe9}, Clock (clock circadian regulator) [NCBI Gene 12753] {aka 5330400M04Rik, KAT13D}, Bmal1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 11865] {aka Arnt3, Arntl, BMAL1b, MOP3, bHLHe5, bmal1b'}
- **Diseases:** memory impairment (MESH:D008569)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11897300/full.md

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Source: https://tomesphere.com/paper/PMC11897300