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Exercise increases mTOR signaling in brain regions involved in cognition and emotional behavior.
Lloyd, Brian A; Hake, Holly S; Ishiwata, Takayuki; Farmer, Caroline E; Loetz, Esteban C; Fleshner, Monika; Bland, Sondra T; Greenwood, Benjamin N.
Afiliação
  • Lloyd BA; Department of Psychology, University of Colorado Denver, United States.
  • Hake HS; Department of Psychology, University of Colorado Denver, United States.
  • Ishiwata T; Department of Sport and Wellness, Rikkyo University, Saitama, Japan.
  • Farmer CE; Department of Psychology, University of Colorado Denver, United States.
  • Loetz EC; Department of Psychology, University of Colorado Denver, United States.
  • Fleshner M; Department of Integrative Physiology and Center for Neuroscience, University of Colorado Boulder, United States.
  • Bland ST; Department of Psychology, University of Colorado Denver, United States.
  • Greenwood BN; Department of Psychology, University of Colorado Denver, United States. Electronic address: benjamin.greenwood@ucdenver.edu.
Behav Brain Res ; 323: 56-67, 2017 04 14.
Article em En | MEDLINE | ID: mdl-28130174
ABSTRACT
Exercise can enhance learning and memory and produce resistance against stress-related psychiatric disorders such as depression and anxiety. In rats, these beneficial effects of exercise occur regardless of exercise controllability both voluntary and forced wheel running produce stress-protective effects. The mechanisms underlying these beneficial effects of exercise remain unknown. The mammalian target of rapamycin (mTOR) is a translation regulator important for cell growth, proliferation, and survival. mTOR has been implicated in enhancing learning and memory as well as antidepressant effects. Moreover, mTOR is sensitive to exercise signals such as metabolic factors. The effects of exercise on mTOR signaling, however, remain unknown. The goal of the present study was to test the hypothesis that exercise, regardless of controllability, increases levels of phosphorylated mTOR (p-mTOR) in brain regions important for learning and emotional behavior. Rats were exposed to 6 weeks of either sedentary (locked wheel), voluntary, or forced wheel running conditions. At 6 weeks, rats were sacrificed during peak running and levels of p-mTOR were measured using immunohistochemistry. Overall, both voluntary and forced exercise increased p-mTOR-positive neurons in the medial prefrontal cortex, striatum, hippocampus, hypothalamus, and amygdala compared to locked wheel controls. Exercise, regardless of controllability, also increased numbers of p-mTOR-positive glia in the striatum, hippocampus, and amygdala. For both neurons and glia, the largest increase in p-mTOR positive cells was observed after voluntary running, with forced exercise causing a more modest increase. Interestingly, voluntary exercise preferentially increased p-mTOR in astrocytes (GFAP+), while forced running increased p-mTOR in microglia (CD11+) in the inferior dentate gyrus. Results suggest that mTOR signaling is sensitive to exercise, but subtle differences exist depending on exercise controllability. Increases in mTOR signaling could contribute to the beneficial effects of exercise on cognitive function and mental health.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Cognição / Emoções / Serina-Treonina Quinases TOR / Atividade Motora / Neurônios Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Cognição / Emoções / Serina-Treonina Quinases TOR / Atividade Motora / Neurônios Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article