Developmental effects of wheel running on hippocampal glutamate receptor expression in young and mature adult rats

• Published in: Neuroscience Vol. 305; pp. 248 - 256
• Main Authors: Staples, M.C., Somkuwar, S.S., Mandyam, C.D.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Ltd 01.10.2015
• Subjects: Age Factors; aging; Aging - physiology; Analysis of Variance; Animals; Animals, Newborn; Body Weight; Circadian Rhythm; dorsal; exercise; Gene Expression Regulation - physiology; GluN receptor; hippocampus; Hippocampus - growth & development; Hippocampus - metabolism; Male; Neurology; Physical Conditioning, Animal - physiology; Rats; Rats, Wistar; Receptors, Glutamate - metabolism; Running - physiology; Statistics as Topic; Time Factors; ventral; dorsal; VH; DH; hippocampus; BDNF; GluN receptor; ventral; LTP; exercise; aging; GluN; ventral hippocampus; dorsal hippocampus; glutamatergic ionotropic N-methyl-d-aspartate receptor; brain-derived neurotrophic factor; long-term potentiation
• ISSN: 0306-4522; 1873-7544; 1873-7544
• DOI: 10.1016/j.neuroscience.2015.07.058

•Young adult runners escalate running activity.•Age is a factor in the hippocampal GluN response to voluntary wheel running.•GluN response is subregionally distinct within the hippocampus. Recent evidence suggests that the behavioral benefits associated with voluntary wheel running in rodents may be due to modulation of glutamatergic transmission in the hippocampus, a brain region implicated in learning and memory. However, the expression of the glutamatergic ionotropic N-methyl-d-aspartate receptor (GluN) in the hippocampus in response to chronic sustained voluntary wheel running has not yet been investigated. Further, the developmental effects during young and mature adulthood on wheel running output and GluN expression in hippocampal subregions has not been determined, and therefore is the main focus of this investigation. Eight-week-old and 16-week-old male Wistar rats were housed in home cages with free access to running wheels and running output was monitored for 4weeks. Wheel access was terminated and tissues from the dorsal and ventral hippocampi were processed for Western blot analysis of GluN subunit expression. Young adult runners demonstrated an escalation in running output but this behavior was not evident in mature adult runners. In parallel, young adult runners demonstrated a significant increase in total GluN (1 and 2A) subunit expression in the dorsal hippocampus (DH), and an opposing effect in the ventral hippocampus (VH) compared to age-matched sedentary controls; these changes in total protein expression were not associated with significant alterations in the phosphorylation of the GluN subunits. In contrast, mature adult runners demonstrated a reduction in total GluN2A expression in the DH, without producing alterations in the VH compared to age-matched sedentary controls. In conclusion, differential running activity-mediated modulation of GluN subunit expression in the hippocampal subregions was revealed to be associated with developmental effects on running activity, which may contribute to altered hippocampal synaptic activity and behavioral outcomes in young and mature adult subjects.