Running reduces stress and enhances cell genesis in aged mice
Received 14 October 2009; received in revised form 17 December 2009; accepted 23 December 2009. published online 27 January 2010. Corrected Proof
Abstract
Cell proliferation and neurogenesis are diminished in the aging mouse dentate gyrus. However, it is not known whether isolated or social living affects cell genesis and stress levels in old animals. To address this question, aged (17–18 months old) female C57Bl/6 mice were single or group housed, under sedentary or running conditions. We demonstrate that both individual and socially housed aged C57Bl/6 mice have comparable basal cell proliferation levels and demonstrate increased running-induced cell genesis. To assess stress levels in young and aged mice, corticosterone (CORT) was measured at the onset of the active/dark cycle and 4h later. In young mice, no differences in CORT levels were observed as a result of physical activity or housing conditions. However, a significant increase in stress in socially housed, aged sedentary animals was observed at the onset of the dark cycle; CORT returned to basal levels 4h later. Together, these results indicate that voluntary exercise reduces stress in group housed aged animals and enhances hippocampal cell proliferation.
aDivision of Medical Sciences, University of Victoria, Victoria, BC, Canada
bThe Program in Neuroscience, University of British Columbia, Vancouver, BC, Canada
cThe Department of Cellular and Physiological Sciences, University of British Columbia, Vancouver, BC, Canada
dLaboratory of Genetics, Salk Institute for Biological Studies, La Jolla, CA, USA
eLaboratory of Neurosciences, National Institute on Aging, Baltimore, MD, USA
Corresponding author at: Neuroplasticity and Behavior Unit, Laboratory of Neurosciences, Suite 100, Biomedical Research Center, National Institute on Aging (NIA), 251 Bayview Boulevard, Baltimore, MD 21224, USA. Tel.: +410 558 8064.