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Intact glucosinolates modulate hepatic cytochrome P450 and phase II conjugation activities and may contribute directly to the chemopreventive activity of cruciferous vegetables.

Authors :
Abdull Razis AF
Bagatta M
De Nicola GR
Iori R
Ioannides C
Source :
Toxicology [Toxicology] 2010 Nov 09; Vol. 277 (1-3), pp. 74-85. Date of Electronic Publication: 2010 Sep 15.
Publication Year :
2010

Abstract

The currently accepted view is that the chemopreventive activity of glucosinolates is exclusively mediated by their degradation products, such as isothiocyanates. In the present study, evidence is presented for the first time that intact glucosinolates can modulate carcinogen-metabolising enzyme systems. The glucosinolates glucoraphanin and glucoerucin were isolated from cruciferous vegetables and incubated with precision-cut rat liver slices. Both glucosinolates elevated the O-dealkylations of methoxy- and ethoxyresorufin, markers for CYP1 activity; supplementation of the incubation medium with myrosinase, the enzyme that converts glucosinolates to their corresponding isothiocyanates, abolished these effects. Moreover, both glucoerucin and glucoraphanin increased the apoprotein levels of microsomal CYP1A1, CYP1A2 and CYP1B1. At higher concentrations, both glucosinolates enhanced quinone reductase activity, whereas glucoraphanin also elevated glutathione S-transferase; in this instance, however, supplementation of the incubation medium with myrosinase exacerbated the inductive effect. Finally, both glucosinolates increased modestly cytosolic quinone reductase, GSTĪ± and GSTĪ¼ protein levels, which became more pronounced when myrosinase was added to the incubations with the glucosinolate. It may be inferred that intact glucosinolates can modulate the activity of hepatic carcinogen-metabolising enzyme systems and this is likely to impact on the chemopreventive activity linked to cruciferous vegetable consumption.<br /> (Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1879-3185
Volume :
277
Issue :
1-3
Database :
MEDLINE
Journal :
Toxicology
Publication Type :
Academic Journal
Accession number :
20833222
Full Text :
https://doi.org/10.1016/j.tox.2010.08.080