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Involvement of β 3 -adrenergic receptor activation via cyclic GMP- but not NO-dependent mechanisms in human corpus cavernosum function
Author(s) -
Giuseppe Cirino,
Raffaella Sorrentino,
Roberta d’Emmanuele di Villa Bianca,
Ada Popolo,
Alessandro Palmieri,
Ciro Imbimbo,
Ferdinando Fusco,
Nicola Longo,
G Tajana,
Louis J. Ignarro,
Vincenzo Mirone
Publication year - 2003
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0931347100
Subject(s) - endocrinology , medicine , receptor , adrenergic receptor , agonist , signal transduction , biology , beta adrenergic receptor kinase , g protein coupled receptor , chemistry , microbiology and biotechnology
The beta(3)-adrenoreceptor plays a major role in lipolysis but the role and distribution of beta(3)-receptors in other specific sites have not been extensively studied. beta(3)-adrenergic receptors are present not only in adipose tissue but also in human gall bladder, colon, prostate, and skeletal muscle. Recently, beta(3)-adrenergic receptor stimulation was shown to elicit vasorelaxation of rat aorta through the NO-cGMP signal transduction pathway. Here we show that beta(3)-receptors are present in human corpus cavernosum and are localized mainly in smooth muscle cells. After activation by a selective beta(3)-adrenergic receptor agonist, BRL 37344, there was a cGMP-dependent but NO-independent vasorelaxation that was selectively blocked by a specific beta(3)-receptor antagonist. In addition, we report that the human corpus cavernosum exhibits basal beta(3)-receptor-mediated vasorelaxant tone and that beta(3)-receptor activity is linked to inhibition of the RhoA/Rho-kinase pathway. These observations indicate that beta(3)-receptors may play a physiological role in mediating penile erection and, therefore, could represent a therapeutic target for treatment of erectile dysfunction.

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