PMID- 22813995 OWN - NLM STAT- MEDLINE DCOM- 20130124 LR - 20230113 IS - 1873-7544 (Electronic) IS - 0306-4522 (Linking) VI - 222 DP - 2012 Oct 11 TI - Effects of voluntary running on plasma levels of neurotrophins, hippocampal cell proliferation and learning and memory in stressed rats. PG - 289-301 LID - 10.1016/j.neuroscience.2012.07.019 [doi] AB - Previous studies have shown that a 2-week treatment with 40 mg/kg corticosterone (CORT) in rats suppresses hippocampal neurogenesis and decreases hippocampal brain-derived neurotrophic factor (BDNF) levels and impairs spatial learning, all of which could be counteracted by voluntary wheel running. BDNF and insulin-like growth factor (IGF-1) have been suggested to mediate physical exercise-enhanced hippocampal neurogenesis and cognition. Here we examined whether such running-elicited benefits were accompanied by corresponding changes of peripheral BDNF and IGF-1 levels in a rat model of stress. We examined the effects of acute (5 days) and chronic (4 weeks) treatment with CORT and/or wheel running on (1) hippocampal cell proliferation, (2) spatial learning and memory and (3) plasma levels of BDNF and IGF-1. Acute CORT treatment improved spatial learning without altered cell proliferation compared to vehicle treatment. Acute CORT-treated non-runners showed an increased trend in plasma BDNF levels together with a significant increase in hippocampal BDNF levels. Acute running showed no effect on cognition, cell proliferation and peripheral BDNF and IGF-1 levels. Conversely, chronic CORT treatment in non-runners significantly impaired spatial learning and suppressed cell proliferation in association with a decreased trend in plasma BDNF level and a significant increase in hippocampal BDNF levels. Running counteracted cognitive deficit and restored hippocampal cell proliferation following chronic CORT treatment; but without corresponding changes in plasma BDNF and IGF-1 levels. The results suggest that the beneficial effects of acute stress on cognitive improvement may be mediated by BDNF-enhanced synaptic plasticity that is hippocampal cell proliferation-independent, whereas chronic stress may impair cognition by decreasing hippocampal cell proliferation and BDNF levels. Furthermore, the results indicate a trend in changes of plasma BDNF levels associated with a significant alteration in hippocampal levels, suggesting that treatment with running/CORT for 4 weeks may induce a change in central levels of hippocampal BDNF level, which may not lead to a significant change in peripheral levels. CI - Copyright (c) 2012 IBRO. Published by Elsevier Ltd. All rights reserved. FAU - Yau, S-Y AU - Yau SY AD - Department of Anatomy, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region. FAU - Lau, B W-M AU - Lau BW FAU - Zhang, E-D AU - Zhang ED FAU - Lee, J C-D AU - Lee JC FAU - Li, A AU - Li A FAU - Lee, T M C AU - Lee TM FAU - Ching, Y-P AU - Ching YP FAU - Xu, A-M AU - Xu AM FAU - So, K-F AU - So KF LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120717 PL - United States TA - Neuroscience JT - Neuroscience JID - 7605074 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Nerve Growth Factors) RN - 67763-96-6 (Insulin-Like Growth Factor I) RN - G34N38R2N1 (Bromodeoxyuridine) RN - WI4X0X7BPJ (Hydrocortisone) SB - IM MH - Animals MH - Body Weight/physiology MH - Brain-Derived Neurotrophic Factor/metabolism MH - Bromodeoxyuridine MH - Cell Differentiation/physiology MH - *Cell Proliferation MH - Fluorescent Antibody Technique MH - Hippocampus/*cytology MH - Hydrocortisone/metabolism MH - Immunohistochemistry MH - Insulin-Like Growth Factor I/metabolism MH - Learning/*physiology MH - Male MH - Maze Learning/physiology MH - Memory/*physiology MH - Nerve Growth Factors/*blood MH - Organ Size/physiology MH - Physical Conditioning, Animal/physiology MH - Rats MH - Rats, Sprague-Dawley MH - Running/*psychology MH - Stress, Psychological/blood/*psychology MH - Taste/drug effects/physiology EDAT- 2012/07/21 06:00 MHDA- 2013/01/25 06:00 CRDT- 2012/07/21 06:00 PHST- 2012/03/02 00:00 [received] PHST- 2012/07/06 00:00 [revised] PHST- 2012/07/08 00:00 [accepted] PHST- 2012/07/21 06:00 [entrez] PHST- 2012/07/21 06:00 [pubmed] PHST- 2013/01/25 06:00 [medline] AID - S0306-4522(12)00726-9 [pii] AID - 10.1016/j.neuroscience.2012.07.019 [doi] PST - ppublish SO - Neuroscience. 2012 Oct 11;222:289-301. doi: 10.1016/j.neuroscience.2012.07.019. Epub 2012 Jul 17.