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.
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Authors | N Sasaki, E Uchida, M Niiyama, T Yoshida, M Saito |
Journal | The Journal of veterinary medical science
(J Vet Med Sci)
Vol. 60
Issue 4
Pg. 465-9
(Apr 1998)
ISSN: 0916-7250 [Print] Japan |
PMID | 9592719
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 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
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Topics |
- Adipose Tissue, Brown
(drug effects, 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, veterinary)
- RNA, Messenger
(biosynthesis)
- Receptors, Adrenergic, beta
(physiology)
- Receptors, Adrenergic, beta-3
- Transcription, Genetic
(drug effects)
- Uncoupling Protein 1
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