Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/93477
Type: Artigo
Title: Effects of β-adrenoceptor antagonists in the neural nitric oxide release induced by electrical field stimulation and sodium channel activators in the rabbit corpus cavernosum
Author: Baracat, J.S.
Arantes, E.C.
Teixeira, C.E.
De Nucci, G.
Antunes, E.
Abstract: β-Adrenoceptor antagonists may present receptor-independent mechanisms, such as blockade of voltage-gated sodium channels. This study aimed to investigate the effects of non-selective (propranolol), and selective β1- (atenolol, metoprolol and betaxolol) and β2-adrenoceptor (ICI 118,551) antagonists in the nitric oxide (NO)-mediated rabbit corpus cavernosum relaxations induced by either electrical field stimulation (EFS) or activators of voltage-gated sodium channels. The sodium channel blockers tetrodotoxin and saxitoxin abolished the relaxations induced by EFS or sodium channel activators of binding site-2 (aconitine and veratridine), site-3 (Ts3 toxin), site-4 (Ts1 toxin) and site-5 (brevetoxin-3). The β-adrenoceptor antagonists failed to affect the relaxations induced by EFS, aconitine and veratridine. Relaxations induced by Ts3 and Ts1 toxins, as well as brevetoxin-3, were markedly reduced by prior addition of propranolol, betaxolol and ICI 118,551. During the established relaxation induced by Ts3 toxin, propranolol failed to restore the basal tone. In conclusion, β-adrenoceptor antagonists may cause an allosteric inhibition at the binding site-3, -4 and -5 of voltage-gated sodium channels, leading to blockade of neural NO release
Subject: Óxido nítrico
Neurônios nitrérgicos
Country: Países Baixos
Editor: Elsevier
Citation: European Journal Of Pharmacology. , v. 519, n. 1-2, p. 146 - 153, 2005.
Rights: fechado
Identifier DOI: 10.1016/j.ejphar.2005.07.011
Address: https://www.sciencedirect.com/science/article/pii/S0014299905007417
Date Issue: 2005
Appears in Collections:FCM - Artigos e Outros Documentos

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