Effects of β2-agonists and exercise on β2-adrenergic receptor signaling in skeletal muscles

  • Sato Shogo
    Laboratory of Physiological Sciences, Faculty of Human Sciences, Waseda University Japan Society for the Promotion of Science
  • Shirato Ken
    Laboratory of Physiological Sciences, Faculty of Human Sciences, Waseda University
  • Kizaki Takako
    Department of Molecular Predictive Medicine and Sport Science, Kyorin University, School of Medicine
  • Ohno Hideki
    Department of Molecular Predictive Medicine and Sport Science, Kyorin University, School of Medicine
  • Tachiyashiki Kaoru
    Department of Natural and Living Sciences, Graduate School of Education, Joetsu University of Education
  • Imaizumi Kazuhiko
    Laboratory of Physiological Sciences, Faculty of Human Sciences, Waseda University Global COE Doctoral Program, Graduate School of Sport Sciences, Waseda University

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タイトル別名
  • Effects of β<sub>2</sub>-agonists and exercise on β<sub>2</sub>-adrenergic receptor signaling in skeletal muscles

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In this review, we discuss the anabolic and metabolic responses of skeletal muscles to β2-agonists and exercise. β2-agonists increase muscle mass, particularly in fast-twitch muscles. Exercise positively regulates glucose homeostasis, mitochondrial biogenesis, and metabolic enzyme levels in skeletal muscles; whereas treatment with β2-agonists attenuates these beneficial effects. This review also describes the role of β2-adrenergic receptor (β2-AR) signaling molecules, such as cyclic adenosine monophosphate response element-binding protein, mitogen-activated protein kinase, and Akt/protein kinase B, in the response of skeletal muscles to β2-agonist treatment and exercise. For example, β2-agonists and exercise increase the phosphorylation of p38 mitogen-activated protein kinase in slow-twitch muscles. Our interpretation of these findings is that β2-adrenergic receptor signaling plays a functional role in the anabolic and metabolic responses of skeletal muscles to β2-agonists and exercise.

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