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胺碘酮对胃肠平滑肌的解痉作用:钙的可能参与

Antispasmodic effect of amiodarone on gastrointestinal smooth muscle: possible involvement of calcium.

作者信息

Gaion R M, Basadonna O, Santostasi G, Fantin M, Maragno I, Dorigo P

机构信息

Department of Pharmacology, University of Padova, Italy.

出版信息

Arch Int Pharmacodyn Ther. 1988 Jul-Aug;294:112-24.

PMID:3233045
Abstract

The influence of amiodarone on contractions induced by acetylcholine (ACh) was studied in isolated preparations of guinea-pig ileum, duodenum and stomach fundus as well as in rat stomach fundus. In the guinea-pig ileum a concentration-dependent antispasmodic effect of amiodarone (20-70 microM) was observed after 30 min exposure to the drug, but not after 15 min. The inhibition of ACh-induced contraction further increased with time after removal of amiodarone from the bathing fluid. Similar results were obtained in ileum preparations maintained in a low Ca2+ medium (0.35 mM CaCl2) and under these conditions the response to ACh was restored by washing the tissue with a normal Ca2+ medium (1.4 mM CaCl2). Both low Ca2+ and amiodarone depressed the tonic component of ACh-induced contraction more than the phasic one. Guinea-pig duodenum was more susceptible than the ileum to the antispasmodic action of amiodarone and again this effect was slow in onset and not reversible. The highest inhibition of ACh-induced contractions by amiodarone was obtained in guinea-pig stomach fundus. In these preparations treated with a low amiodarone concentration (20 microM) the response to ACh was restored after drug removal. In rat stomach fundus the effect of amiodarone was low and not reversible. Like amiodarone, Ca2+ lowering caused a decrease in the response to ACh with the following order of effectiveness: guinea-pig stomach greater than guinea-pig duodenum greater than guinea-pig ileum greater than rat stomach. The inhibitions caused by amiodarone and by low Ca2+ were always additive. These results indicate that amiodarone exerts an antispasmodic effect on the gastrointestinal tract and that regional and species differences exist for this action. The possible involvement of Ca2+ in this effect is discussed.

摘要

在豚鼠回肠、十二指肠和胃底以及大鼠胃底的离体标本中研究了胺碘酮对乙酰胆碱(ACh)诱导的收缩的影响。在豚鼠回肠中,暴露于该药物30分钟后观察到胺碘酮(20 - 70 microM)具有浓度依赖性的解痉作用,但15分钟后未观察到。从浴液中去除胺碘酮后,ACh诱导的收缩抑制作用随时间进一步增强。在低钙培养基(0.35 mM CaCl2)中维持的回肠标本中获得了类似结果,在这些条件下,用正常钙培养基(1.4 mM CaCl2)冲洗组织可恢复对ACh的反应。低钙和胺碘酮对ACh诱导收缩的强直成分的抑制作用比对相性成分的抑制作用更强。豚鼠十二指肠比回肠对胺碘酮的解痉作用更敏感,而且这种作用起效缓慢且不可逆。胺碘酮对豚鼠胃底中ACh诱导的收缩的抑制作用最强。在这些用低浓度胺碘酮(20 microM)处理的标本中,去除药物后对ACh的反应得以恢复。在大鼠胃底中,胺碘酮的作用较弱且不可逆。与胺碘酮一样,降低钙离子浓度会导致对ACh的反应降低,其效力顺序如下:豚鼠胃>豚鼠十二指肠>豚鼠回肠>大鼠胃。胺碘酮和低钙引起的抑制作用总是相加的。这些结果表明,胺碘酮对胃肠道发挥解痉作用,并且该作用存在区域和物种差异。讨论了钙离子可能参与这种作用的情况。

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