Anti-obesity effects of selective agonists to the β3-adrenergic receptor in dogs(2)Recruitment of thermogenic brown adipocytes and reduction of adiposity after chronic treatment with a β3-adrenergic agonist

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  • SASAKI Noriyasu
    Laboratory of Biochemistry, Department of Biomedical Sciences, School of Veterinary Medicine, Hokkaido University
  • UCHIDA Eiji
    Department of Internal Medicine II, Rakuno Gakuen University
  • NIIYAMA Masayoshi
    Department of Internal Medicine II, Rakuno Gakuen University
  • YOSHIDA Toshihide
    Department of Internal Medicine, Kyoto Prefectural University of Medicine
  • SAITO Masayuki
    Laboratory of Biochemistry, Department of Biomedical Sciences, School of Veterinary Medicine, Hokkaido University

書誌事項

タイトル別名
  • Anti-Obesity Effects of Selective Agonists to the .BETA.3-Adrenergic Receptor in Dogs. II. Recruitment of Thermogenic Brown Adipocytes and Reduction of Adiposity after Chronic Treatment with a .BETA.3-Adrenergic Agonist.
  • Anti-obesity effects of selective agoni
  • Anti-obesity effects of selective agonists to β3-adrenergic receptor in dogs. II. Recruitment of thermogenic brown adipocytes and reduction of adiposity after chronic treatment with a β3-adrenergic agonist

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The aim of this study was to evaluate the effectiveness of β3-adrenergic agonists for the treatment and prevention of obesity in the dog. When a selective β3-adrenergic agonist, CL316, 243 (0.1 mg/kg), was given orally to adult beagles every day for 5-7 weeks, body weight and girth were decreased compared with control placebo-treated dogs. Gross anatomical examinations revealed no noticeable abnormalities in CL316, 243-treated dogs, except an apparent decrease in abdominal fat. Immunohistochemical examination of perirenal adipose tissue showed a remarkable increase in brown adipocytes expressing a thermogenic protein, uncoupling protein (UCP). The increased expression of UCP and its mRNA in CL316, 243-treated dogs was also confirmed by Western blot and reverse transcription polymerase chain reaction analyses. It was concluded that treatment with a β3-adrenergic agonist stimulates UCP expression, which may lead to an increase in energy expenditure, and thereby is useful for the treatment and prevention of obesity in the dog.

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