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Endocrinology, doi:10.1210/en.2003-0537
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Endocrinology Vol. 144, No. 11 4923-4930
Copyright © 2003 by The Endocrine Society

Direct Effects of Testosterone, 17ß-Estradiol, and Progesterone on Adrenergic Regulation in Cultured Brown Adipocytes: Potential Mechanism for Gender-Dependent Thermogenesis

Marta Monjo, Ana M. Rodríguez, Andreu Palou and Pilar Roca

Laboratori de Bioquímica i Biologia Molecular, Departament de Biologia Fonamental i Ciències de la Salut, Universitat de les Illes Balears, Palma de Mallorca 07071, Spain

Address all correspondence and requests for reprints to: Pilar Roca, Departament de Biologia Fonamental i Ciències de la Salut, Edifici Guillem Colom, Universitat de les Illes Balears, Carretera Valldemossa, Km 7.5, Palma de Mallorca 07071, Spain. E-mail: pilar.roca{at}uib.es.

Previous studies suggest that sex hormones could be responsible, at least in part, for the gender-dependent thermogenesis found in the adrenergic control of brown adipose tissue (BAT) under control conditions and in response to diet and cold. Catecholamines, as well as several hormones, including sex hormones, may alter the function or expression of different adrenoceptor subtypes in brown adipocytes in vivo, and a confirmation could be provided by in vitro experiments. Therefore, the effect of testosterone, 17ß-estradiol, progesterone, and norepinephrine (NE) on adrenergic receptor (AR) gene expression ({alpha}2A-, ß1-, ß2-, and ß3-AR) and lipolytic activity was investigated in differentiated brown adipocytes in culture. We report that the expression of each AR subtype gene was distinctively regulated by NE and sex hormones in brown adipocytes. Testosterone-treated cells had lower lipolytic activity and increased expression of antilipolytic receptors {alpha}2A-AR. Both 17ß-estradiol and progesterone decreased {alpha}2A-AR expression and {alpha}2A3-AR protein ratio, but progesterone had higher potency than 17ß-estradiol, increasing ß-AR levels, mainly ß3-AR expression, and enhancing lipolysis stimulated by NE. In conclusion, our results support the idea that male and female sex hormones, as a part of the hormonal environment of BAT, have direct and opposite effects on the AR balance and lipolytic activity, and they might play a role in the gender dimorphism for the recruitment process in BAT.




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