Abstract

Neurotrophic factors and growth factors are known to have positive effects on hippocampal proliferation. However, previous findings on the effects of these factors on exercise-induced hippocampal proliferation are inconsistent. In this study, we investigated the effects of voluntary running on hippocampal proliferation and the expression levels of nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and insulin-like growth factor 1 (IGF-1) in hippocampus. Twenty-four male C57BL/6 mice were randomly divided into four groups: control groups 1 and 2 (C1, n = 6; C2, n = 6) and running groups 1 and 2 (R1, n = 6; R2, n = 6). Mice from C1 and C2 were placed individually in standard cages for eight weeks; mice from R1 and R2 were housed individually in cages with a running wheel for eight weeks. At the fifth week, C1 and R1 mice were injected with BrdU for 7 consecutive days. On the first day of the ninth week, the C1 and R1 mice were anaesthetized and hippocampal neuronal proliferation was assessed using immunohistochemistry; the mice in C2 and R2 were sacrificed to test the expression levels of NGF, BDNF, and IGF-1 mRNA in hippocampus using RT-PCR. The results indicated that voluntary running significantly increased the number of BrdU-positive cells in the dentate gyrus (DG), and significantly upregulated the levels of NGF, BDNF, and IGF-1 mRNA in the hippocampus. In conclusion, our findings indicated that hippocampal proliferation was enhanced by voluntary running, which was associated with increased NGF, BDNF, and IGF-1 mRNA levels in the hippocampus.

Highlights

  • Many studies have confirmed that neurogenesis continues in discrete regions of the adult brain, especially in the subgranular zone (SGZ) of the dentate gyrus (DG) and the subventricular zone (SVZ) of the lateral ventricles [1, 2]

  • We further investigated the expression levels of nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and insulin-like growth factor 1 (IGF-1) mRNA in the hippocampus

  • There was a significant increase in the NGF mRNA (C2: 1.00 ± 0.34, R2: 3.76 ± 0.47, P < 0.01), BDNF mRNA (C2: 1.00 ± 0.39, R2: 3.56 ± 1.42, P < 0.01), and IGF-1 mRNA (C2: 1.00 ± 0.73, R2: 2.51 ± 0.86, P < 0.01) in the hippocampus of the R2 group compared to that in the C2 group (Fig. 2). These results indicated that voluntary running increased the mRNA expression levels of NGF, BDNF, and IGF-1 in the hippocampus

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Summary

Introduction

Many studies have confirmed that neurogenesis continues in discrete regions of the adult brain, especially in the subgranular zone (SGZ) of the dentate gyrus (DG) and the subventricular zone (SVZ) of the lateral ventricles [1, 2]. Newly generated cells can proliferate, differentiate, mature, and integrate into functional neural networks [3]. Neuronal proliferation plays a vital role in the maintenance of hippocampal structure and function. Some neurotrophic factors or growth factors have been demonstrated to be involved in mediating proliferation in the hippocampus. Birch et al [4] showed that chronic intracerebroventricular infusion of nerve growth factor (NGF) promoted neuronal proliferation in the hippocampal DG. Conditional knockout brain-derived neurotrophic factor (BDNF) resulted in the reduction of hippocampal proliferation [5]. Aberg et al [6] found that insulin-like growth factor 1 (IGF-1) had a direct proliferative effect in adult hippocampal progenitor cells

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