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Biology of Reproduction 66, 508-515 (2002)
© 2002 Society for the Study of Reproduction, Inc.


Regular Article

{alpha}1-Adrenoceptor Subtypes in Rat Epididymis and the Effects of Sexual Maturation1

Daniel B.C. Queiróza, Fúlvio R. Mendesa, Catarina S. Portoa, and Maria Christina W. Avellar2,a

a Section of Experimental Endocrinology, Department of Pharmacology, Universidade Federal de São Paulo-Escola Paulista de Medicina, 04044-020 São Paulo, Brazil

We have characterized the expression of {alpha}1-adrenoceptor in epididymis from rats in different stages of sexual maturation: 40 (immature), 60 (young adult), and 120 (adult) days of age. Plasma testosterone levels were low in the immature animals but increased significantly in the 60- and 120-day-old animals. These changes were followed by a progressive increase in rat body weight and in caput and cauda epididymis relative weight. Reverse transcription polymerase chain reaction assay indicated that {alpha}1a-, {alpha}1b-, and {alpha}1d-adrenoceptor transcripts were present in both caput and cauda epididymis from adult rats. Ribonuclease protection assays further indicated that the expression of these {alpha}1-adrenoceptor transcripts differed with age and epididymal region analyzed. Prazosin (nonselective {alpha}1 antagonist), 5-methyl urapidil ({alpha}1A-selective), and BMY 7378 ({alpha}1D-selective) displaced [3H]prazosin binding curves in caput and cauda epididymis from 40- and 120-day-old rats. The potency order for these antagonists, as calculated from the negative logarithm of the inhibition constant (pKi) values for the high-affinity sites, indicated a predominant population of {alpha}1A-adrenoceptor subtype in caput and cauda epididymis from adult animals. Differences in pKi values in caput and cauda epididymis from immature and adult animals also suggested that the relative amount of {alpha}1-adrenoceptors, at the protein level, is modulated by sexual maturation. Taken together, the changes in {alpha}1-adrenoceptor expression during sexual maturation may suggest specific roles for these receptors in epididymal function.

First decision: 30 July 2001.

1 This study was supported in part by Fundação de Amparo à Pesquisa do Estado de São Paulo, Brazil (FAPESP, grant 96/1777-1) and T.W. Fogarty International, USA (subcontract UNC 5-53284); a Master fellowship supported by FAPESP (D.B.C.Q.); and a Researcher fellowship supported by Conselho Nacional do Desenvolvimento Científico e Tecnológico, Brazil (M.C.W.A. and C.S.P.). Part of this work was presented at the 24th annual meeting of the American Society of Andrology, Louisville, KY, 1999.

2 Correspondence: Maria Christina W. Avellar, Department of Pharmacology, Section of Experimental Endocrinology, UNIFESP-Escola Paulista de Medicina, Rua 03 de maio 100, INFAR, Vila Clementino, 04044-020 São Paulo, Brazil. FAX: 55 11 5576 4448; avellar.farm{at}infar.epm.br




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