Biotransformation of Silybin and its Congeners

被引:34
|
作者
Kren, Vladimir [1 ]
Marhol, Petr [1 ]
Purchartova, Katerina [1 ]
Gabrielova, Eva [3 ]
Modriansky, Martin [2 ]
机构
[1] Acad Sci Czech Republ, Ctr Biocatalysis & Biotransformat, Inst Microbiol, CZ-14220 Prague, Czech Republic
[2] Palacky Univ, Fac Med & Dent, Inst Med Chem & Biochem, CZ-77515 Olomouc, Czech Republic
[3] Palacky Univ, Fac Med & Dent, Inst Mol & Translat Med, CZ-77515 Olomouc, Czech Republic
关键词
Biotransformation; cytochrome P450; diastereoisomers; glucuronidation; silibinin; silybin; silymarin; sulfonation; HUMAN UDP-GLUCURONOSYLTRANSFERASES; HUMAN LIVER-MICROSOMES; MILK THISTLE; SILYMARIN FLAVONOLIGNANS; IN-VITRO; PROSTATE-CANCER; ANTIOXIDANT ACTIVITY; CYTOCHROMES P450; DRUG-INTERACTION; RAT-LIVER;
D O I
10.2174/1389200214666131118234507
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Silybin and its congeners belong to a group of flavonolignans with strong biological activities. These compounds are potentially applicable in human medicine, e.g. due to their cytoprotective activity. As a part of herbal preparations available on the open market, they face the risk of potential negative drug-drug interactions. This review aims to evaluate current knowledge on the metabolism of these compounds by biotransformation enzymes, interactions with other drugs, their pharmacokinetics, and bioavailability. While silybin and its derivatives interact with cytochrome P450s, only metabolism of silybin by cytochrome P450 2C8 poses a risk of adverse effects. The main biotransformation route of silybin and derivatives was identified as conjugation, which is stereospecific in case of silybin. Studies of the metabolism, pharmacokinetics, potentional drug - drug interactions and increasing bioavailability of these flavonolignans play an important facet of possible therapeutical use of these compounds. The goal of our review is to aid future developments in the area of silybin research.
引用
收藏
页码:1009 / 1021
页数:13
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