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Signal transduction pathways involved in kinin B(2) receptor-mediated vasodilation in the rat isolated perfused kidney.
Bagaté, K; Grima, M; Imbs, J L; Jong, W D; Helwig, J J; Barthelmebs, M.
Afiliação
  • Bagaté K; Institut de Pharmacologie, Faculté de Médecine, 11 rue Humann, 67085 Strasbourg Cedex, France.
Br J Pharmacol ; 132(8): 1735-42, 2001 Apr.
Article em En | MEDLINE | ID: mdl-11309245
ABSTRACT
The signal transduction pathways involved in kinin B(2) receptor-related vasodilation were investigated in rat isolated perfused kidneys. During prostaglandin F(2alpha) or KCl-induced constriction, the vasodilator response to a selective B(2) receptor agonist, Tyr(Me)(8)bradykinin (Tyr(Me)(8)BK), was assessed. Tyr(Me)(8)BK produced a concentration- and endothelium-dependent relaxation that was decreased by about 30 - 40% after inhibition of nitric oxide (NO) synthase by N(G)-nitro-L-arginine (L-NOARG) or of cyclo-oxygenase by indomethacin; a greater decrease (about 40 - 50%) was observed after concomitant inhibition of the two pathways. High extracellular K(+) diminished Tyr(Me)(8)BK-induced relaxation by about 75% suggesting a major contribution of endothelium-derived hyperpolarization. The residual response was almost completely suppressed by NO synthase and cyclo-oxygenase inhibition. The K(+) channel inhibitors, tetrabutylammonium (non-specific) and charybdotoxin (specific for Ca(2+)-activated K(+) channel), suppressed Tyr(Me)(8)BK-induced relaxation resistant to L-NOARG and indomethacin. Inhibition of cytochrome P450 (clotrimazole or 7-ethoxyresorufin) decreased the NO/prostanoids-independent relaxation to Tyr(Me)(8)BK by more than 60%, while inhibition of the cannabinoid CB(1) receptor (SR 141716A) had only a moderate effect. Acetylcholine induced a concentration-dependent relaxation with characteristics nearly similar to the response to Tyr(Me)(8)BK. In contrast, the relaxation elicited by sodium nitroprusside was potentiated in the absence of NO (L-NOARG or removal of endothelium) but remained unchanged otherwise. These results indicate that the activation of kinin B(2) receptors in the rat isolated kidney elicits an endothelium-dependent vasorelaxation, mainly dependent on the activation of charybdotoxin-sensitive Ca(2+)-activated K(+) channels. In addition, cytochrome P450 derivatives appear to be involved.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Circulação Renal / Vasodilatação / Transdução de Sinais / Receptores da Bradicinina Limite: Animals Idioma: En Revista: Br J Pharmacol Ano de publicação: 2001 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Circulação Renal / Vasodilatação / Transdução de Sinais / Receptores da Bradicinina Limite: Animals Idioma: En Revista: Br J Pharmacol Ano de publicação: 2001 Tipo de documento: Article País de afiliação: França