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Eur J Pharmacol ; 256(3): 329-33, 1994 May 02.
Artigo em Inglês | MEDLINE | ID: mdl-8045278

RESUMO

Radioligand binding assays were performed with the selective antagonist of dihydropyridine-sensitive Ca2+ channels [3H]PN200-110 (isradipine) in rat vas deferens, before and 7 days after denervation, and data were compared with those obtained for K(+)-induced contractions, which are Ca(2+)-dependent. The density (Bmax) of dihydropyridine binding sites was decreased to almost one-third of its normal value after denervation. The respective affinity (KD) was not significantly changed. In addition, it was observed that the K(+)-induced tonic contraction, which corresponded to 55 +/- 2% of the respective phasic contraction, was decreased to 41 +/- 3% after denervation. It is assumed that the decreased density of Ca2+ channels causes a decrease in K(+)-induced influx of Ca2+ and consequently of the corresponding tonic contraction. These results indicate that autonomic innervation can regulate the density of dihydropyridine-sensitive Ca2+ channels in the rat vas deferens.


Assuntos
Isradipino/metabolismo , Ducto Deferente/metabolismo , Animais , Sítios de Ligação/efeitos dos fármacos , Canais de Cálcio/efeitos dos fármacos , Denervação , Di-Hidropiridinas/farmacologia , Masculino , Contração Muscular/efeitos dos fármacos , Cloreto de Potássio/farmacologia , Ratos , Ratos Wistar , Ducto Deferente/efeitos dos fármacos
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