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依匹斯汀对组胺、血小板活化因子和5-羟色胺诱导的豚鼠和大鼠支气管收缩的抑制作用。

Inhibitory effect of epinastine on bronchoconstriction induced by histamine, platelet activating factor and serotonin in guinea pigs and rats.

作者信息

Tasaka K, Kamei C, Nakamura S

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Japan.

出版信息

Arzneimittelforschung. 1994 Mar;44(3):327-9.

PMID:7910745
Abstract

Effects of epinastine ((+/-)-3-amino-9,13b-dihydro-1H-dibenz[c,f]imidazo[1,5-a]azepine hydrochloride, WAL 801 CL, CAS 80012-43-7) and reference drugs on bronchoconstriction induced by histamine, platelet activating factor (PAF) and serotonin were studied in guinea pigs and rats. Oral administration of epinastine resulted in a potent inhibition on bronchoconstriction induced by all three bronchoconstrictor agents, and especially, an inhibitory effect on histamine-induced response was remarkable. The effect of epinastine was stronger than that of ketotifen in inhibiting the responses induced by both PAF and serotonin. However, the extent of inhibition in the latter was less remarkable than that seen after histamine. Azelastine was 1.36-4.57 times less potent than epinastine in inhibiting the bronchoconstriction induced by either bronchospasmogen. Although promethazine displayed inhibitory effects on the responses induced by histamine, PAF and serotonin, the inhibiting potency was distinctly inferior to that of epinastine.

摘要

研究了依巴斯汀((+/-)-3-氨基-9,13b-二氢-1H-二苯并[c,f]咪唑并[1,5-a]氮杂卓盐酸盐,WAL 801 CL,CAS 80012-43-7)及对照药物对组胺、血小板活化因子(PAF)和5-羟色胺诱导的豚鼠和大鼠支气管收缩的影响。口服依巴斯汀可有效抑制这三种支气管收缩剂诱导的支气管收缩,尤其是对组胺诱导反应的抑制作用显著。依巴斯汀在抑制PAF和5-羟色胺诱导的反应方面比酮替芬更强。然而,对后者的抑制程度不如组胺诱导反应后明显。氮卓斯汀在抑制任何一种支气管痉挛原诱导的支气管收缩方面比依巴斯汀效力低1.36至4.57倍。尽管异丙嗪对组胺、PAF和5-羟色胺诱导的反应有抑制作用,但其抑制效力明显低于依巴斯汀。

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