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二巯基丁二醇立体异构体在实验性胃溃疡中的不同保护作用。

Different protective effects of dimercapto-butanediol stereoisomers in experimental gastric ulceration.

作者信息

Balint G A, Varró V

出版信息

Arch Int Pharmacodyn Ther. 1983 Sep;265(1):115-8.

PMID:6651399
Abstract

The erythro version of 1, 4,-dimercapto-2, 3,-butanediol provided a significant protection against experimental gastric ulcer induced by indomethacin, while it was ineffective in stress ulcer of rats. The threo version of the same compound showed a complete ineffectiveness. It seems that most probably there is a specific receptor system in the living organism where only the erythro version is effective. Moreover, there was a remarkable difference between indomethacin-induced and stress ulcer as far as their protection is concerned. Sulfhydryl containing substances inhibited indomethacin ulcer but they were ineffective against stress ulcer. This experimental result provides further data for the difference of the pathomechanism of various experimental ulcers and thus their direct extrapolation to the human disease and to its treatment needs extreme caution.

摘要

1,4 - 二巯基 - 2,3 - 丁二醇的赤藓醇型对消炎痛诱导的实验性胃溃疡有显著保护作用,但对大鼠应激性溃疡无效。同一化合物的苏阿糖型则完全无效。似乎在生物体中很可能存在一种特定的受体系统,只有赤藓醇型在其中有效。此外,就消炎痛诱导的溃疡和应激性溃疡的保护作用而言,存在显著差异。含巯基物质可抑制消炎痛诱导的溃疡,但对应激性溃疡无效。这一实验结果为各种实验性溃疡发病机制的差异提供了进一步的数据,因此将其直接外推至人类疾病及其治疗需要极其谨慎。

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