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cis- and trans-Resveratrol Are Glucuronidated in Rat Brain, Olfactory Mucosa and Cultured Astrocytes.

Authors :
Sabolovic, Nicole
Heurtaux, Tony
Humbert, Anne-Claude
Krisa, Stéphanie
Magdalou, Jacques
Source :
Pharmacology; 2007, Vol. 80 Issue 2/3, p185-192, 8p, 5 Graphs
Publication Year :
2007

Abstract

Background/Aims: Glucuronidation of cis- and trans-resveratrol (3,5,4’-trihydroxy-trans-stilbene), which is a naturally occurring phytoalexin known to exert a number of beneficial health effects, was investigated in rat brain, cultured astrocytes and olfactory mucosa. Methods: The isomers were incubated with tissue homogenates, microsomes, or rat liver recombinant UDP-glucuronosyltransferases in the presence of UDP-glucuronic acid. The glucuronides were separated by HPLC and quantitated. Astrocytes were exposed to lipopolysaccharide to promote inflammatory conditions. Results: All tissues were able to form resveratrol glucuronides although at a lower extent, when compared to the liver. The reaction was stereo- and regioselective. In brain tissue, trans-resveratrol 3-O-glucuronide was mainly formed, whereas the cis-isomer was glucuronidated at a lower rate on that position. No 4’-O-glucuronide was detected in brain. In olfactory mucosa homogenates, the cis 3-O-glucuronide was mainly formed, whereas the trans-isomer was glucuronidated only on the 3-position. In astrocytes, 3-O-glucuronides of the cis- and trans-resveratrol were only detected. The rat recombinant UGT1A6 and UGT2B1 isoforms were able to glucuronidate cis- and trans-resveratrol. Finally, in inflammatory conditions, trans-resveratrol glucuronidation was enhanced in astrocytes. Conclusion: Brain tissues are effective in the glucuronidation of resveratrol isomers. This metabolism pathway is likely to modulate the concentration of these biologically active substances. Copyright © 2007 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00317012
Volume :
80
Issue :
2/3
Database :
Complementary Index
Journal :
Pharmacology
Publication Type :
Academic Journal
Accession number :
26088534
Full Text :
https://doi.org/10.1159/000104149