The Peripheral Circadian Clock and Exercise: Lessons from Young and Old Mice. Issue 1 (16th December 2020)

• Record Type: Journal Article
• Authors: Bruns, Danielle R.; Yusifova, Musharraf; Marcello, Nicholas A.; Green, Carly J.; Walker, Whitney J.; Schmitt, Emily E.
• Is Part Of: Journal of circadian rhythms. Volume 18:Issue 1(2020)
• Publication Date: 2020-12-16
• Subjects: circadian rhythm -- exercise -- aging; Circadian rhythms -- Periodicals; 571.77
• DOI: 10.5334/jcr.201
• Languages: English
• ISSNs: 1740-3391

Abstract

Critical biological processes are under control of the circadian clock. Disruption of this clock, e.g. during aging, results in increased risk for development of chronic disease. Exercise is a protective intervention that elicits changes in both age and circadian pathologies, yet its role in regulating circadian gene expression in peripheral tissues is unknown. We hypothesized that voluntary wheel running would restore disrupted circadian rhythm in aged mice. We analyzed wheel running patterns and expression of circadian regulators in male and female C57Bl/6J mice in adult (~4 months) and old (~18 months) ages. As expected, young female mice ran further than male mice, and old mice ran significantly less than young mice. Older mice of both sexes had a delayed start time in activity which likely points to a disrupted diurnal running pattern and circadian disruption. Voluntary wheel running rescued some circadian dysfunction in older females. This effect was not present in older males, and whether this was due to low wheel running distance or circadian output is not clear and warrants a future study. Overall, we show that voluntary wheel running can rescue some circadian dysfunction in older female but not male mice; and these changes are tissue dependent. While voluntary running was not sufficient to fully rescue age-related changes in circadian rhythm, ongoing studies will determine if forced exercise (e.g. treadmill) and/or chrono-timed exercise can improve age-related cardiovascular, skeletal muscle, and circadian dysfunction.