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2-取代噻唑烷-4(R)-羧酸对小鼠肝脏和大脑中非蛋白质巯基水平及硫转移酶活性的影响。

The effect of 2-substituted thiazolidine-4(R)-carboxylic acids on non-protein sulphydryl levels and sulphurtransferase activities in mouse liver and brain.

作者信息

Włodek L, Radomski J, Wróbel M

机构信息

Institute of Medical Biochemistry, Medical Academy, Kraków, Poland.

出版信息

Biochem Pharmacol. 1993 Jul 6;46(1):190-3.

PMID:8347132
Abstract

2-Substituted thiazolidine-4(R)-carboxylic acids (TD) were found to increase the concentration of non-protein sulphydryls (NPSH) and the activity of rhodanese (thiosulphate sulphurtransferase, EC 2.8.1.1) and 3-mercaptopyruvate sulphurtransferase (EC 2.8.1.2) in mouse liver. These properties suggest TDs are potentially hepatoprotective compounds. However TDs also cause depletion of NPSH in the mouse brain and this may be the reason for their toxic side effects on the central nervous system.

摘要

已发现2-取代噻唑烷-4(R)-羧酸(TD)可提高小鼠肝脏中非蛋白质巯基(NPSH)的浓度以及硫代硫酸硫转移酶(硫代硫酸盐硫转移酶,EC 2.8.1.1)和3-巯基丙酮酸硫转移酶(EC 2.8.1.2)的活性。这些特性表明TD可能是具有肝脏保护作用的化合物。然而,TD也会导致小鼠大脑中NPSH的消耗,这可能是它们对中枢神经系统产生毒副作用的原因。

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