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美喹他嗪(LM - 209)的药理学研究(I)。化学介质的拮抗作用(作者译)

[Pharmacological study of mequitazine (LM-209) (I). Antagonistic actions of chemical mediators (author's transl)].

作者信息

Fujimura H, Tsurumi K, Yanagihara M, Hiramatsu Y, Tamura Y, Shimizu Y, Hojo M, Yoshida Y

出版信息

Nihon Yakurigaku Zasshi. 1981 Oct;78(4):279-89.

PMID:6120126
Abstract

Antagonistic activities of Mequitazine (LM-209) on chemical mediators and in particular histamine were investigated in guinea-pigs, mice and rats. The antagonistic activity of LM-209 for histamine in the isolated ileum and trachea of guinea-pigs was less potent than that for clemastine fumarate (CL) and chlorpheniramine maleate (CPM) while that for acetylcholine was more potent than CL and CPM. Moreover, the antagonistic activities of these three compounds on serotonin and bradykinin were almost equipotent in the excised ileum. Using a modified Konzett-Rössler method, the bronchodilating effect of LM-209 (p.o.) for histamine was same as CL, but that for acetylcholine was more potent than CL and CPM. The protective activity of LM-209 (p.o.) on acute death induced by histamine and metacholine in mice was the same as CL, but the duration of the anti-histaminic action was markedly longer than CL. LM-209 given orally inhibited markedly the increased vascular permeability by histamine in rats and the diarrhea by 5-HTP in mice, but did not affect on the histamine-induced ulcer in guinea-pigs. From these results, LM-209 appears to have potent and long acting antagonistic activity on various chemical mediators.

摘要

在豚鼠、小鼠和大鼠中研究了美喹他嗪(LM - 209)对化学介质尤其是组胺的拮抗活性。LM - 209对豚鼠离体回肠和气管中组胺的拮抗活性比富马酸氯马斯汀(CL)和马来酸氯苯那敏(CPM)弱,而对乙酰胆碱的拮抗活性比CL和CPM强。此外,这三种化合物对5 - 羟色胺和缓激肽的拮抗活性在离体回肠中几乎相当。采用改良的Konzett - Rössler方法,LM - 209(口服)对组胺的支气管扩张作用与CL相同,但对乙酰胆碱的作用比CL和CPM更强。LM - 209(口服)对小鼠组胺和醋甲胆碱诱导的急性死亡的保护活性与CL相同,但抗组胺作用的持续时间明显长于CL。口服给予LM - 209可显著抑制大鼠组胺引起的血管通透性增加和小鼠5 - 羟色胺引起的腹泻,但对豚鼠组胺诱导的溃疡无影响。从这些结果来看,LM - 209似乎对各种化学介质具有强效且长效的拮抗活性。

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