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维拉帕米和沙丁胺醇单独及联合应用对组胺诱导的豚鼠离体气管收缩的抗痉挛和解痉作用。

Antispasmogenic and spasmolytic effects of verapamil and salbutamol, alone and in combination, on histamine-induced guinea pig tracheal contraction in vitro.

作者信息

Valcheva S, Belcheva A

机构信息

Department of Pharmacology, Medical University of Varna, Bulgaria.

出版信息

Agents Actions. 1994 Jun;41 Spec No:C108-10. doi: 10.1007/BF02007789.

Abstract

The antispasmogenic and spasmolytic effects of the calcium entry blocker verapamil were examined on histamine-induced guinea pig tracheal contraction in vitro in comparison with the beta 2-adrenergic agonist salbutamol. The effects of verapamil were found to be about 1000 times weaker than those of salbutamol. The antispasmogenic IC50 for verapamil was 1.99 x 10(-4) M compared to 7.94 x 10(-8) M for salbutamol. The spasmolytic EC50 for verapamil was 3.37 x 10(-5) M and for salbutamol was 1.95 x 10(-8) M. The combined application of verapamil and salbutamol resulted in additive antispasmogenic and spasmolytic effects.

摘要

将钙通道阻滞剂维拉帕米的抗痉挛和缓解痉挛作用与β2肾上腺素能激动剂沙丁胺醇进行比较,在体外研究了其对组胺诱导的豚鼠气管收缩的影响。发现维拉帕米的作用比沙丁胺醇弱约1000倍。维拉帕米的抗痉挛IC50为1.99×10(-4)M,而沙丁胺醇为7.94×10(-8)M。维拉帕米的解痉EC50为3.37×10(-5)M,沙丁胺醇为1.95×10(-8)M。维拉帕米和沙丁胺醇联合应用产生了相加的抗痉挛和解痉作用。

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