Children’s Nutrition Research Center Staff Publications

Language

English

Publication Date

6-1-2022

Journal

Pharmacology Biochemistry and Behavior

DOI

10.1016/j.pbb.2022.173388

PMID

35447158

PMCID

PMC9422145

PubMedCentral® Posted Date

8-29-2022

PubMedCentral® Full Text Version

Author MSS

Abstract

Age-related cognitive decline and disruptions in circadian rhythms are growing problems as the average human life span increases. Multiple strains of the senescence-accelerated mouse (SAM) show reduced life span, and the SAMP8 strain in particular has been well documented to show cognitive deficits in behavior as well as a bimodal pattern of circadian locomotor activity. However, little is known about circadian regulation within the hippocampus of these strains of mice. Here we test the hypothesis that in this early senescence model, disruption of the molecular circadian clock in SAMP8 animals drives disrupted behavior and physiology. We found normal rhythms in PER2 protein expression in the SCN of SAMP8 animals at 4 months, despite the presence of disrupted wheel-running activity rhythms at this age. Interestingly, a significant rhythm in PER2 expression was not observed in the hippocampus of SAMP8 animals, despite a significant 24-h rhythm in SAMR1 controls. We also examined time-restricted feeding as a potential strategy to rescue disrupted hippocampal plasticity. Time-restricted feeding increased long-term potentiation at Schaffer collateral-CA1 synapses in SAMP8 mice (compared to SAMR1 controls). Overall, we confirm disrupted circadian locomotor rhythms in this early senescence model (as early as 4 months) and discovered that this disruption is not due to arrhythmic PER2 levels in the SCN; however, other extra-SCN circadian oscillators (i.e., hippocampus) are likely impaired with accelerated aging.

Keywords

Aging, Animals, Circadian Rhythm, Disease Models, Animal, Hippocampus, Long-Term Potentiation, Male, Mice, Circadian rhythms, hippocampus, aging, SAMP8, time-restricted feeding

Published Open-Access

yes

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