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Effects of a beta3-adrenergic agonist on the immune response in diet-induced (cafeteria) obese animals.

Abstract
Molecules with affinity for beta3-adrenoceptors are not only effective anti-obesity agents in rodent models, but may play a role in the regulation of the immune response. The aim of the current investigation was to analyse the effects of trecadrine on the immune response in diet-induced (cafeteria) obese rats. Male Wistar rats were divided into 2 groups, the control group (C, n=9) was fed with the standard pelleted chow laboratory diet, while the other group was fed with a high-fat (cafeteria) diet. Cafeteria-fed rats were divided into two new subgroups (n=9 each), which received either i.p. saline (obese, O) or trecadrine (1mg/kg/day) (obese+trecadrine, O+T) daily for 5 weeks. Lymphocyte subpopulations and the proliferative response were determined by validated procedures. The administration of trecadrine was able to prevent the onset of obesity in cafeteria-fed rats. Trecadrine-treatment to obese animals appeared to improve the number of lymphocyte subpopulations (CD4+ and CD8+) as compared to those animals only receiving the high-fat diet, being the values of the trecadrine-treated animals on the high-fat diet similar to the control rats. However, the lymphoproliferative response when stimulated with several mitogens was markedly reduced by the cafeteria intake and was further decreased by the beta3-adrenergic administration. The spleen mRNA expression level of UCP2, PPARgamma and Ob-Rb were not affected by the trecadrine treatment. Summing up, at the immune system level, trecadrine administration increased the proportion of CD4+ spleen lymphocytes, although it was not able to restore the lymphocyte proliferative response which was depressed.
AuthorsO Lamas, J A Martínez, A Marti
JournalJournal of physiology and biochemistry (J Physiol Biochem) Vol. 59 Issue 3 Pg. 183-91 (Sep 2003) ISSN: 1138-7548 [Print] Spain
PMID15000449 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adrenergic beta-3 Receptor Agonists
  • Adrenergic beta-Agonists
  • Benzyl Alcohols
  • Fatty Acids, Nonesterified
  • Ion Channels
  • Membrane Transport Proteins
  • Mitochondrial Proteins
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Triglycerides
  • Ucp2 protein, rat
  • Uncoupling Protein 2
  • trecadrine
  • Cholesterol
  • Glycerol
Topics
  • Adipose Tissue (drug effects)
  • Adrenergic beta-3 Receptor Agonists
  • Adrenergic beta-Agonists (pharmacology)
  • Animal Feed
  • Animals
  • Benzyl Alcohols (pharmacology)
  • Body Weight (drug effects)
  • Cholesterol (blood)
  • Fatty Acids, Nonesterified (blood)
  • Gene Expression (drug effects)
  • Glycerol (blood)
  • Ion Channels
  • Male
  • Membrane Transport Proteins (biosynthesis)
  • Mitochondrial Proteins (biosynthesis)
  • Obesity (blood, drug therapy, immunology)
  • RNA, Messenger (biosynthesis)
  • Rats
  • Rats, Wistar
  • Receptors, Cytoplasmic and Nuclear (biosynthesis)
  • Spleen (cytology, metabolism)
  • T-Lymphocytes, Cytotoxic (drug effects, immunology)
  • T-Lymphocytes, Helper-Inducer (drug effects, immunology)
  • Transcription Factors (biosynthesis)
  • Triglycerides (blood)
  • Uncoupling Protein 2

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