Oltipraz-induced phase 2 enzyme response conserved in cells lacking mitochondrial DNA

被引:12
作者
Chua, YL
Zhang, DW
Boelsterli, U
Moore, PK
Whiteman, M
Armstrong, JS [1 ]
机构
[1] Natl Univ Singapore, Dept Biochem, Singapore 117597, Singapore
[2] Natl Univ Singapore, Dept Pharmacol, Singapore 117597, Singapore
关键词
oltipraz; glutathione; p(0); mtDNA; glutathione S-transferase; mitochondrial permeability transition; reactive oxygen species;
D O I
10.1016/j.bbrc.2005.09.059
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
Oltipraz, a member of a class of 1, 2-dithiolethiones, is a potent phase 2 enzyme inducing agent used as a cancer chemopreventive. In this study, we investigated regulation of the phase 2 enzyme response and protection against endogenous oxidative stress in lymphoblastic leukemic parental CEM cells and cells lacking mitochondrial DNA (mtDNA) (rho(0)) by oltipraz. Glutathione (GSH) levels (total and mitochondrial) and glutathione S-transferase (GST) activity were significantly increased after pretreatment with oltipraz in both parental (rho(+)) and p(0) cells, and both cell lines were resistant to mitochondrial oxidation, loss of mitochondrial membrane potential, and cell death in response to the GSH depleting agent diethylmaleate. These results show that the phase 2 enzyme response, by enhancing GSH-dependent systems involved in xenobiotic metabolism, blocks endogenous oxidative stress and cell death, and that this response is intact in cells lacking mtDNA. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:375 / 381
页数:7
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