Gut micro flora in genesis of methilthyo metabolites of paracetamol

G. Smieško, M. Mikov, Vera Gusman, M. Djanic
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引用次数: 0

Abstract

Gut micro flora represents a system of extensive metabolic capacity which is quite different when compared to other cells of body and organs. In recent times, there has been an evidence of very important role of gut cysteine conjugate beta-lyases in metabolism of cystein conjugates. A lot of studies are dedicated to exploration of the role of gut micro flora in formation of methylthio adducts from paracetamol in conventional mice and those treated with neomycin as our study. A highly significant reduction in urinary excretion of 3-methylthioparacetamol in group of neomycin-treated mice was confirmed as well its glucuronic acid and sulphate conjugates. Following the principal role of gut flora in the C-S cleavage of paracetamol l-3-cyctein it is clear that highest concentration of methylthio adducts from paracetamol are presented in pretreated mice.
对乙酰氨基酚甲基代谢物的肠道菌群成因
肠道菌群是一个具有广泛代谢能力的系统,与人体其他细胞和器官相比有很大的不同。近年来,有证据表明肠道半胱氨酸缀合物β -裂解酶在半胱氨酸缀合物的代谢中起着非常重要的作用。大量的研究致力于探索肠道菌群在常规小鼠和新霉素治疗小鼠体内对乙酰氨基酚甲基硫加合物形成中的作用。新霉素组小鼠尿中3-甲基硫代对乙酰氨基酚及其葡萄糖醛酸和硫酸盐缀合物显著减少。根据肠道菌群在C-S裂解扑热息痛l-3-环蛋白中的主要作用,很明显,预处理小鼠中出现了最高浓度的扑热息痛甲基硫合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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