𝔖 Bobbio Scriptorium
✦   LIBER   ✦

In vitro phase II metabolism of xanthohumol by human UDP-glucuronosyltransferases and sulfotransferases

✍ Scribed by Corinna E. Ruefer; Clarissa Gerhäuser; Norbert Frank; Hans Becker; Sabine E. Kulling


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
306 KB
Volume
49
Category
Article
ISSN
1613-4125

No coin nor oath required. For personal study only.

✦ Synopsis


Xanthohumol (XN) is the principal prenylated flavonoid of the hop plant and has recently gained considerable interest due to its potential cancer-chemopreventive effects. However, the metabolism of XN has not yet been investigated in detail. Therefore, we studied the in vitro phase II metabolism of XN using nine human recombinant UDP-glucuronosyltransferases (UGT) and five sulfotransferases (SULT). The identification of the metabolites formed was elucidated using HPLC with diode array detection as well as HPLC/API-ES MS. XN was efficiently glucuronidated by UGT 1 A 8, 1 A 9, and 1 A 10; further important UGTs were UGT 1 A 1, 1 A 7, and 2 B 7. With respect to the sulfation reaction, SULT 1 A 1*2, 1 A 2, and 1 E 1 were the most active SULT forms. UGT 1 A 3, 1 A 4, and 1 A 6 as well as SULT 1 A 3 and 2 A 1 were of minor importance for the conjugation of XN. Three mono-glucuronides as well as three mono-sulfates were identified. Considering the tissue distribution of the tested UGT and SULT enzyme forms, these findings suggest a prominent role for the glucuronidation and sulfation of XN in the liver as well as in the gastrointestinal tract.


📜 SIMILAR VOLUMES


Stereoselective metabolism of propranolo
✍ Lushan Yu; Minrong Qian; Yao Liu; Tongwei Yao; Su Zeng 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 293 KB

## Abstract Stereoselective metabolism of propranolol side‐chain glucuronidation was studied for two recombinant human uridine diphosphate glucuronosyltransferases (UGTs), UGT1A9 and UGT2B7. The __S__‐ and __R__‐propranolol side‐chain glucuronides produced in the incubation mixtures were assayed si

Glucuronidation of zearalenone, zeranol
✍ Erika Pfeiffer; Andreas Hildebrand; Hannes Mikula; Manfred Metzler 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 223 KB

## Abstract Glucuronidation constitutes an important pathway in the phase II metabolism of the mycotoxin zearalenone (ZEN) and the growth promotor α‐zearalanol (α‐ZAL, zeranol), but the enzymology of their formation is yet unknown. In the present study, ZEN, α‐ZAL and four of their major phase I me

In vitro inhibitory effects of non-stero
✍ Yuji Mano; Takashi Usui; Hidetaka Kamimura 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 102 KB 👁 2 views

The inhibitory potencies of non-steroidal anti-inflammatory drugs (NSAIDs) on UDP-glucuronosyltransferase (UGT) 1A9 activity were investigated in recombinant human UGT1A9 using 4-methylumbelliferone (4-MU) as a substrate for glucuronidation. 4-MU glucuronidation (4-MUG) showed Michaelis-Menten kinet

In vitro metabolism of mirtazapine enant
✍ Seetal Dodd; David W. Boulton; Graham D. Burrows; C. Lindsay De Vane; Trevor R. 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 52 KB 👁 1 views

The metabolism of mirtazapine enantiomers was investigated in vitro using human lymphoblast microsomes transfected with human cDNA to overexpress either CYP1A2, CYP2C9, CYP2C19, CYP2D6 or CYP3A4 and assayed for mirtazapine enantiomers using a validated chiral method of high-performance liquid chroma