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依他尼酸和柳氮磺胺吡啶抑制大鼠胃中白三烯C4的生成:冷束缚应激大鼠可能的胃抗溃疡机制。

Ethacrynic acid and sulphasalazine inhibit the generation of leukotriene C4 in rat stomachs: a possible gastric anti-ulcer mechanism in cold-restraint-stressed rats.

作者信息

Garg G P, Cho C H, Ogle C W

机构信息

Department of Pharmacology, Faculty of Medicine, University of Hong Kong.

出版信息

Pharmacology. 1992;44(4):177-89. doi: 10.1159/000138917.

Abstract

The role of gastric glandular mucosal leukotriene C4 in gastric ulceration, produced by restraint at 4 degrees C (stress) for 2 h in rats, was studied in relation to the ulcer-preventing effects of ethacrynic acid, sulphasalazine and its constituents (sulphapyridine and 5-aminosalicylic acid), AA-861 and ONO-1078. Stress itself significantly raised mucosal leukotriene C4 levels; pretreatment with ethacrynic acid, sulphasalazine, sulphapyridine or AA-861 antagonised these changes and reduced the severity of gastric ulceration. Mucosal mast cell degranulation was prevented by ethacrynic acid, sulphasalazine, 5-aminosalicylic acid, AA-861 or ONO-1078; the mucus-depleting effect of stress was also reversed by all these drugs, except for 5-aminosalicylic acid. The anti-ulcer effect of ethacrynic acid and sulphasalazine appears to be related to their influence on glandular mucosal leukotriene C4 levels.

摘要

研究了大鼠在4℃(应激)下束缚2小时所产生的胃溃疡中胃腺黏膜白三烯C4的作用,以及与依他尼酸、柳氮磺胺吡啶及其成分(磺胺吡啶和5-氨基水杨酸)、AA-861和ONO-1078的抗溃疡作用的关系。应激本身显著提高黏膜白三烯C4水平;依他尼酸、柳氮磺胺吡啶、磺胺吡啶或AA-861预处理可拮抗这些变化并减轻胃溃疡的严重程度。依他尼酸、柳氮磺胺吡啶、5-氨基水杨酸、AA-861或ONO-1078可防止黏膜肥大细胞脱颗粒;除5-氨基水杨酸外,所有这些药物均可逆转应激的黏液消耗作用。依他尼酸和柳氮磺胺吡啶的抗溃疡作用似乎与其对腺黏膜白三烯C4水平的影响有关。

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