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尼索地平对5-羟色胺和钾离子诱导的猪冠状动脉和股动脉收缩的抑制作用。

Inhibitory effects of nisoldipine on serotonin and potassium induced contractions of porcine coronary and femoral arteries.

作者信息

Kazda S

机构信息

Institute of Pharmacology, Bayer AG, Wuppertal, Fed. Rep. of Germany.

出版信息

Arzneimittelforschung. 1991 Mar;41(3):204-7.

PMID:1867655
Abstract

The inhibitory effect of nisoldipine (Baymycard, Syscor; CAS 63675-72-9) and nifedipine on the serotonin and potassium induced contractions of porcine coronary and femoral arteries in vitro has been investigated. Both nisoldipine and nifedipine inhibited preferentially the serotonin induced contraction in the coronary artery being less effective in the inhibition of the femoral artery. The coronary selectivity of nisoldipine is at least 10 times more pronounced than that of nifedipine. The serotonin antagonist ketanserin inhibited contractions on both vessels with the same potency. The potassium induced contraction was inhibited by the dihydropyridines in both coronary and femoral artery. Nisoldipine again, was more potent than nifedipine in the inhibition of coronary artery spasm but not in the contraction of femoral artery. Ketanserin did not inhibit contractions of any vessels.

摘要

已研究了尼索地平(拜米卡德,西斯科;CAS 63675-72-9)和硝苯地平对体外猪冠状动脉和股动脉中5-羟色胺和钾诱导的收缩的抑制作用。尼索地平和硝苯地平均优先抑制冠状动脉中5-羟色胺诱导的收缩,而对股动脉的抑制作用较弱。尼索地平的冠状动脉选择性比硝苯地平至少强10倍。5-羟色胺拮抗剂酮色林对两种血管收缩的抑制作用效力相同。二氢吡啶类药物在冠状动脉和股动脉中均抑制钾诱导的收缩。同样,尼索地平在抑制冠状动脉痉挛方面比硝苯地平更有效,但在抑制股动脉收缩方面并非如此。酮色林不抑制任何血管的收缩。

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