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8-羟基喹啉的解痉和抗炎活性

[Spasmolytic and anti-inflammatory activity of 8-hydroxyquinolines].

作者信息

Zaks A S, Zil'ber A L, Kapitonenko T A

出版信息

Farmakol Toksikol. 1984 Sep-Oct;47(5):44-7.

PMID:6238840
Abstract

It has been shown that quinozole (aqueous solution), enteroseptol and nitroxoline (suspension with Tween-80) in a concentration of 0.2 X 10(-6)-1.10(-5) decrease the tone of the rat and guinea-pig ileum and diminish their peristalsis. When administered in the same concentrations quinozole removes or prevents the spasmogenic effects of barium chloride (1 X 10(-5)-4.10(-5), of histamine (2 X 10(-5) and -6) but not of acetylcholine (1 X 10(-6)). When administered orally in a dose 50 mg/kg to rats enteroseptol and nitroxoline inhibit the serotonin-, agar- and carrageenin-induced edemas of the rat paws without changing the response to subplantar injection of histamine. The data obtained should be taken into consideration during the use of 8-hydroxyquinolines as antimicrobial substances.

摘要

已经表明,浓度为0.2×10⁻⁶ - 1×10⁻⁵的喹诺唑(水溶液)、肠复康和硝咯喹啉(吐温80混悬液)可降低大鼠和豚鼠回肠的张力并减弱其蠕动。当以相同浓度给药时,喹诺唑可消除或预防氯化钡(1×10⁻⁵ - 4×10⁻⁵)、组胺(2×10⁻⁵和 - 6)但不能预防乙酰胆碱(1×10⁻⁶)的致痉作用。当以50mg/kg的剂量口服给予大鼠时,肠复康和硝咯喹啉可抑制5-羟色胺、琼脂和角叉菜胶诱导的大鼠爪水肿,而不改变对足底注射组胺的反应。在将8-羟基喹啉用作抗菌物质时应考虑所获得的数据。

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