SR59230A blocks β3-adrenoceptor-linked modulation of uncoupling protein-1 and leptin in rat brown adipocytes

Cristina Tonello, Laura Dioni, Luca Briscini, Enzo Nisoli, Michele O. Carruba

Research output: Contribution to journalArticlepeer-review


Experimental evidence suggests that, by stimulating energy expenditure in brown fat, selective β3-adrenoceptor agonists can reduce body weight in obese rodents. In order to investigate further the physiological role of β3-adrenoceptors in brown adipocytes, we analysed the effects of selective β3-adrenoceptor agonists and antagonists on uncoupling protein-1 and leptin gene expression in culture-differentiated brown fat cells. Our main findings were that: (i) the leptin gene is expressed in brown adipocytes; (ii) the selective β3-adrenoceptor agonist, N[(2S)-7-carbethoxy-1,2,3,4-tetrahydronaphth-2-yl]-(2R)-2-hydroxy-2-(3-chlorophenil)ethanamine hydrochloride (SR58611A), inhibits leptin gene while inducing uncoupling protein-1 gene expression; (iii) these opposite effects of SR58611A are antagonized by the selective β3-adrenoceptor antagonist, SS-enantiomer 3-(2-ethylphenoxy)-1-(1S)1,2,3,4-tetrahydronaphth-1-ylaminol]-(2S)-2-propanol oxalate (SR59230A), but not by the selective β1-adrenoceptor antagonist (±)-[2-(3-carbamoyl-4-hydroxyphenoxy)-ethylamino]-3-[4(1-methyl-4-trifluoromethyl-2-imidazolyl)-phenoxy]-2 propanol (CGP20712A); and (iv) these effects are due to increased cyclic AMP levels. These results confirm by means of a different experimental approach that β3-adrenoceptors play a central role in controlling the expression of genes that are important for brown fat function. Copyright (C) 1998 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)125-129
Number of pages5
JournalEuropean Journal of Pharmacology
Issue number1
Publication statusPublished - Jul 3 1998


  • β-Adrenoceptor
  • Brown adipose tissue
  • Leptin
  • Uncoupling protein-1

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Pharmacology

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