exercise;
defensive behavior;
rat;
elevated plus maze;
open field;
social interaction;
conditioned freezing;
D O I:
10.1016/j.brainres.2004.05.086
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
In order to better understand the behavioral adaptations induced by physical activity, this set of experiments assessed the effects of two modes of running exercise on a battery of behavioral tests. The effects of 8 weeks of forced treadmill running and voluntary wheel running on behavior measures in the elevated plus maze, open field, social interaction and conditioned freezing paradigms were investigated. Eight weeks of treadmill running did not alter behavior in any test paradigm. Rats given unrestricted access to running wheels (WR) had a lower percent open ann time (6.0 +/- 2.3%) compared to locked wheel controls (LC) (20.7 +/- 5.7%) in the elevated plus maze. WR also showed decreased entries into center (0.2 +/- 0.2) and crossed fewer lines (61.0 +/- 14.9) in the open field compared to control groups. Both WR and LC groups showed increased social interaction; however, these differences are attributed to housing conditions. The effects of 4 weeks of wheel running on elevated plus maze and open field behavior were also investigated to address the possibility of a temporal effect of exercise on behavior. Four weeks of wheel running produced behavioral changes in the open field similar to those found at 8 weeks, but not in the elevated plus maze suggesting a temporal effect of wheel running on plus maze behavior. The behavioral adaptations found after 4 and 8 weeks of wheel running were not due solely to enriched environment and appear to be indicative of enhanced defensive behavior. (C) 2004 Elsevier B.V. All rights reserved.
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Cheeta, S
;
Irvine, E
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机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Irvine, E
;
File, SE
论文数: 0引用数: 0
h-index: 0
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Cheeta, S
;
Irvine, E
论文数: 0引用数: 0
h-index: 0
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England
Irvine, E
;
File, SE
论文数: 0引用数: 0
h-index: 0
机构:
Kings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, EnglandKings Coll London, GKT Sch Biomed Sci, Ctr Neurosci, Psychopharmacol Res Unit, London SE1 1UL, England