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

J Vet Med Sci. 1998 Apr;60(4):465-9. doi: 10.1292/jvms.60.465.

Abstract

The aim of this study was to evaluate the effectiveness of beta 3-adrenergic agonists for the treatment and prevention of obesity in the dog. When a selective beta 3-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 beta 3-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.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue, Brown / drug effects
  • Adipose Tissue, Brown / physiology*
  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Body Constitution
  • Body Weight / drug effects
  • Carrier Proteins / biosynthesis
  • Dioxoles / pharmacology*
  • Dog Diseases*
  • Dogs
  • Female
  • Gene Expression Regulation / drug effects
  • Ion Channels
  • Male
  • Membrane Proteins / biosynthesis
  • Mitochondrial Proteins
  • Obesity / prevention & control
  • Obesity / veterinary*
  • RNA, Messenger / biosynthesis
  • Receptors, Adrenergic, beta / physiology*
  • Receptors, Adrenergic, beta-3
  • Transcription, Genetic / drug effects
  • Uncoupling Protein 1

Substances

  • Adrenergic beta-Agonists
  • Carrier Proteins
  • Dioxoles
  • Ion Channels
  • Membrane Proteins
  • Mitochondrial Proteins
  • RNA, Messenger
  • Receptors, Adrenergic, beta
  • Receptors, Adrenergic, beta-3
  • Uncoupling Protein 1
  • disodium (R,R)-5-(2-((2-(3-chlorophenyl)-2-hydroxyethyl)-amino)propyl)-1,3-benzodioxole-2,3-dicarboxylate