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大鼠肝脏对黄酮类化合物槲皮素和儿茶素的硫酸化作用。

Sulphation of the flavonoids quercetin and catechin by rat liver.

作者信息

Shali N A, Curtis C G, Powell G M, Roy A B

机构信息

Department of Biochemistry, University of Wales, College of Cardiff, UK.

出版信息

Xenobiotica. 1991 Jul;21(7):881-93. doi: 10.3109/00498259109039528.

Abstract
  1. The isolated perfused rat liver forms three sulphated metabolites from each of the flavonoids, quercetin and catechin: these are secreted into the bile and the perfusate. 2. Quercetin gives two double conjugates, containing sulphate and glucuronic acid, and one sulphate: catechin gives one such double conjugate and two sulphates. 3. This sulphation is not inhibited by 60 microM 2,6-dichloro-4-nitrophenol which almost completely inhibits the sulphation of harmol in this perfused liver system. 4. The sulphation of harmol by the perfused liver is not inhibited by the flavonoids. 5. Unfractionated sulphotransferases from rat liver catalyse sulphate conjugation of quercetin and catechin in vitro by a reaction inhibited by pentachlorophenol or dichloronitrophenol: the flavonoids inhibit the sulphation of 4-nitrophenol by this system. 6. The results with the two systems are discussed and shown to be compatible.
摘要
  1. 分离灌注的大鼠肝脏能从黄酮类化合物槲皮素和儿茶素中分别形成三种硫酸化代谢产物:这些产物分泌到胆汁和灌注液中。2. 槲皮素产生两种包含硫酸和葡萄糖醛酸的双共轭物以及一种硫酸盐;儿茶素产生一种此类双共轭物和两种硫酸盐。3. 60微摩尔的2,6 - 二氯 - 4 - 硝基苯酚几乎完全抑制该灌注肝脏系统中去甲骆驼蓬碱的硫酸化,但对这种硫酸化没有抑制作用。4. 灌注肝脏对去甲骆驼蓬碱的硫酸化不受黄酮类化合物的抑制。5. 大鼠肝脏的未分级硫酸转移酶在体外催化槲皮素和儿茶素的硫酸结合反应,该反应受五氯苯酚或二氯硝基苯酚抑制:黄酮类化合物抑制该系统对4 - 硝基苯酚的硫酸化。6. 对这两种系统的结果进行了讨论,并表明它们是相符的。

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