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[双西芬及其结构前体对炎症和疼痛反应的影响]

[Effect of diucifon and its structural precursors on inflammatory and pain reactions].

作者信息

Gorbunov S M, Anan'ev E V, Zobov V V, Iakubov Sh M

出版信息

Farmakol Toksikol. 1985 Nov-Dec;48(6):44-7.

PMID:3878798
Abstract

The anti-inflammatory and analgesic action of diucifon, methyluracil and 4,4'-diaminodiphenylsulfone (DDS) was studied in comparison with some nonsteroid preparations. In three traditional models of agar, kaolin and carrageenan paw edema and in the models of analgesia (convulsions, induced by intraabdominal administration of acetic acid to mice and hyperalgesia according to Randall-Selitto's test in rats), diucifon proved more active than its precursors. In Randall-Selitto's test the efficiency of diucifon was 1.5 times less than that of butadione but 24 times higher than that of methyluracil; DDS had no analgetic activity. Diucifon, methyluracil and DDS did not exert any ulcerogenic action.

摘要

将双氯芬、甲基尿嘧啶和4,4'-二氨基二苯砜(DDS)的抗炎和镇痛作用与一些非甾体制剂进行了比较研究。在琼脂、高岭土和角叉菜胶致爪肿胀的三种传统模型以及镇痛模型(给小鼠腹腔注射醋酸诱导惊厥,以及根据兰德尔-塞利托试验在大鼠中诱导痛觉过敏)中,双氯芬比其前体更具活性。在兰德尔-塞利托试验中,双氯芬的效率比布他酮低1.5倍,但比甲基尿嘧啶高24倍;DDS没有镇痛活性。双氯芬、甲基尿嘧啶和DDS均未产生任何致溃疡作用。

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