http://www.sciencedirect.com/science/article/pii/S0304394013000220
Abstract
Recently,
we reported that voluntary resistance wheel running with a resistance
of 30% of body weight (RWR), which produces shorter distances but higher
work levels, enhances spatial memory associated with hippocampal
brain-derived neurotrophic factor (BDNF) signaling compared to wheel
running without a load (WR) (Lee et al., 2012). We thus hypothesized
that RWR promotes adult hippocampal neurogenesis (AHN) as a neuronal
substrate underlying this memory improvement. Here we used 10-week-old
male Wistar rats divided randomly into sedentary (Sed), WR, and RWR
groups. All rats were injected intraperitoneally with the thymidine
analogue 5-Bromo-2′-deoxuridine (BrdU) for 3 consecutive days before
wheel running. We found that even when the average running distance
decreased by about half, the average work levels significantly increased
in the RWR group, which caused muscular adaptation (oxidative capacity)
for fast-twitch plantaris muscle without causing any negative stress
effects. Additionally, immunohistochemistry revealed that the total BrdU+ cells and newborn mature cells (BrdU+/NeuN+)
in the dentate gyrus increased in both the WR and RWR groups. These
results provide new evidence that RWR has beneficial effects on AHN
comparable to WR, even with short running distances.
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