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FCE 20700是一种具有细胞保护作用的前列腺素E2衍生物,它不会干扰吲哚美辛的抗炎活性。

FCE 20700, a cytoprotective PGE2 derivative, does not interfere with the antiinflammatory activity of indomethacin.

作者信息

Ceserani R, Arrigoni C, Mizzotti B, Tremolada L, Ferrari M, Buttinoni A

出版信息

Int J Tissue React. 1983;5(4):349-51.

PMID:6689489
Abstract

A study was made of the interaction between FCE 20700 (11-deoxy-13,14-didehydro-16(S)-methyl-PGE2 methylester) at a fixed dose of 250 mcg/kg and the ulcerogenic and antiinflammatory effect of indomethacin (I) on rat carrageenin paw edema. The combination tested showed the same antiinflammatory effect as I alone: potency ratio FCE 20700 + I/I was 1.03, demonstrating the lack of interaction between the two compounds. Moreover the gastric lesions in FCE 20700 + I treated rats were markedly reduced, allowing the dosage of I to be increased by about three times without increasing its ulcerogenic effect.

摘要

研究了固定剂量为250 mcg/kg的FCE 20700(11-脱氧-13,14-二脱氢-16(S)-甲基前列腺素E2甲酯)与吲哚美辛(I)对大鼠角叉菜胶足肿胀的致溃疡和抗炎作用之间的相互作用。所测试的组合显示出与单独使用I相同的抗炎作用:FCE 20700 + I/I的效价比为1.03,表明这两种化合物之间没有相互作用。此外,FCE 20700 + I处理的大鼠的胃部损伤明显减少,使得I的剂量可以增加约三倍而不增加其致溃疡作用。

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