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黄酮类化合物对人酚磺基转移酶的影响:在药物代谢和化学预防中的潜力。

The effects of flavonoids on human phenolsulphotransferases: potential in drug metabolism and chemoprevention.

作者信息

Ghazali R A, Waring R H

机构信息

School of Biochemistry, University of Birmingham, Edgbaston, United Kingdom.

出版信息

Life Sci. 1999;65(16):1625-32. doi: 10.1016/s0024-3205(99)00423-3.

Abstract

Flavonoids are frequently found in fruits and vegetables, and are currently under investigation as potential chemopreventive agents. The present study reports the inhibitory effects of six flavonoids, quercetin, genistein, daidzein, equol, (+)-catechin and flavone, on sulphation of p-nitrophenol, a model substrate for the P-form of PST (thermostable, TS) and dopamine, a model substrate for the M-form of PST (thermolabile, TL). Kinetic studies of the PST activity and the inhibitory effects of flavonoids on the P-form of PST activity (using Hanes-Wolf and Dixon plots) show low Km and Ki values. Quercetin was found to be the most potent inhibitor and flavone was the least active inhibitor among the flavonoids. Kinetic analysis showed that the inhibition was non-competitive and Ki values were determined for each flavonoid. These observations suggest the potential for clinically important pharmacological and toxicological interactions by flavonoids.

摘要

黄酮类化合物常见于水果和蔬菜中,目前作为潜在的化学预防剂正在研究中。本研究报告了六种黄酮类化合物,即槲皮素、染料木黄酮、大豆苷元、雌马酚、(+)-儿茶素和黄酮,对对硝基苯酚硫酸化作用的抑制效果,对硝基苯酚是P型硫酸转移酶(热稳定型,TS)的模型底物,以及对多巴胺硫酸化作用的抑制效果,多巴胺是M型硫酸转移酶(热不稳定型,TL)的模型底物。对硫酸转移酶活性以及黄酮类化合物对P型硫酸转移酶活性的抑制作用进行动力学研究(使用Hanes-Wolf和Dixon作图法),结果显示Km和Ki值较低。在这些黄酮类化合物中,槲皮素被发现是最有效的抑制剂,而黄酮是活性最低的抑制剂。动力学分析表明,这种抑制作用是非竞争性的,并确定了每种黄酮类化合物的Ki值。这些观察结果表明黄酮类化合物在临床上可能存在重要的药理和毒理相互作用。

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