Running enhances neurogenesis, learning, and long-term potentiation in mice.

Running increases neurogenesis in the dentate gyrus of the hippocampus, a brain structure that is important for memory function. Consequently, spatial learning and long-term potentiation (LTP) were tested in groups of mice housed either with a running wheel (runners) or under standard conditions (controls). Mice were injected with bromodeoxyuridine to label dividing cells and trained in the Morris water maze. LTP was studied in the dentate gyrus and area CA1 in hippocampal slices from these mice. Running improved water maze performance, increased bromodeoxyuridine-positive cell numbers, and selectively enhanced dentate gyrus LTP. Our results indicate that physical activity can regulate hippocampal neurogenesis, synaptic plasticity, and learning.

[1]  T. Bliss,et al.  Reduction of long‐term potentiation in the dentate gyrus of the rat following selective depletion of monoamines. , 1983, The Journal of physiology.

[2]  J. Kauer,et al.  Perturbed dentate gyrus function in serotonin 5-HT2C receptor mutant mice. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[3]  J. Kesslak,et al.  Spatial learning and physical activity contribute to the induction of fibroblast growth factor: neural substrates for increased cognition associated with exercise , 1998, Neuroscience.

[4]  Richard F. Thompson,et al.  Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus. , 1989, Science.

[5]  E. Gould,et al.  Learning enhances adult neurogenesis in the hippocampal formation , 1999, Nature Neuroscience.

[6]  G Buzsáki,et al.  Sustained activation of hippocampal pyramidal cells by ‘space clamping’ in a running wheel , 1999, The European journal of neuroscience.

[7]  E. Gould,et al.  Neurogenesis in adulthood: a possible role in learning , 1999, Trends in Cognitive Sciences.

[8]  B. L. McNaughton,et al.  Evidence for two physiologically distinct perforant pathways to the fascia dentata , 1980, Brain Research.

[9]  G. L. Brown,et al.  Conduction in the cervical sympathetic , 1934, The Journal of physiology.

[10]  F. Gage,et al.  Multipotent progenitor cells in the adult dentate gyrus. , 1998, Journal of neurobiology.

[11]  P. Schwartzkroin,et al.  Neurotrophin expression in rat hippocampal slices: A stimulus paradigm inducing LTP in CA1 evokes increases in BDNF and NT-3 mRNAs , 1992, Neuron.

[12]  J. Korf,et al.  Exposure to chronic psychosocial stress and corticosterone in the rat: Effects on spatial discrimination learning and hippocampal protein kinase Cγ immunoreactivity , 1997, Hippocampus.

[13]  M. Luskin,et al.  Strategies utilized by migrating neurons of the postnatal vertebrate forebrain , 1998, Trends in Neurosciences.

[14]  F. Gage,et al.  More hippocampal neurons in adult mice living in an enriched environment , 1997, Nature.

[15]  F. Gage,et al.  Running increases cell proliferation and neurogenesis in the adult mouse dentate gyrus , 1999, Nature Neuroscience.

[16]  J. Krebs,et al.  Hippocampal growth and attrition in birds affected by experience. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[17]  F. Gage,et al.  Isolation, Characterization and Utilization of CNS Stem Cells , 1997, Research and Perspectives in Neurosciences.

[18]  J. Wehner,et al.  Physical activity enhances spatial learning performance with an associated alteration in hippocampal protein kinase C activity in C57BL/6 and DBA/2 mice , 1993, Brain Research.

[19]  K. Beck,et al.  Estradiol Enhances Learning and Memory in a Spatial Memory Task and Effects Levels of Monoaminergic Neurotransmitters , 1998, Hormones and Behavior.

[20]  R. Morris Developments of a water-maze procedure for studying spatial learning in the rat , 1984, Journal of Neuroscience Methods.

[21]  B. Johansson,et al.  Environment, Social Interaction, and Physical Activity as Determinants of Functional Outcome after Cerebral Infarction in the Rat , 1996, Experimental Neurology.

[22]  C. Cotman,et al.  Exercise and brain neurotrophins , 1995, Nature.

[23]  F. Chaouloff Effects of acute physical exercise on central serotonergic systems. , 1997, Medicine and science in sports and exercise.

[24]  B. McEwen Stress and hippocampal plasticity. , 1999, Annual review of neuroscience.

[25]  T. Bliss,et al.  A synaptic model of memory: long-term potentiation in the hippocampus , 1993, Nature.

[26]  F. Gage,et al.  Amelioration of cholinergic neuron atrophy and spatial memory impairment in aged rats by nerve growth factor , 1987, Nature.

[27]  W. Greenough,et al.  Exercise and the Brain: Angiogenesis in the Adult Rat Cerebellum after Vigorous Physical Activity and Motor Skill Learning , 1992, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[28]  E. Schuman Neurotrophin regulation of synaptic transmission , 1999, Current Opinion in Neurobiology.

[29]  J. Bronzino,et al.  Maturation of long‐term potentiation in the hippocampal dentate gyrus of the freely moving rat , 1994, Hippocampus.

[30]  R. Malenka,et al.  Mechanisms underlying induction of long-term potentiation in rat medial and lateral perforant paths in vitro. , 1993, Journal of neurophysiology.

[31]  E Gould,et al.  Estrogen Stimulates a Transient Increase in the Number of New Neurons in the Dentate Gyrus of the Adult Female Rat , 1999, The Journal of Neuroscience.