Regulation of iNOS expression and glutathione levels in rat liver by oxygen tension

被引:32
作者
Miralles, C
Busquets, X
Santos, C
Togores, B
Hussain, S
Rahman, I
MacNee, W
Agustí, AGN
机构
[1] Hosp Univ Son Dureta, Unidad Invest, Palma de Mallorca, Spain
[2] Hosp Univ Son Dureta, Serv Pneumol, Palma de Mallorca, Spain
[3] McGill Univ, Div Pulm & Crit Care Med, Montreal, PQ, Canada
[4] Univ Edinburgh, ELEGI, Edinburgh, Midlothian, Scotland
[5] Univ Edinburgh, Colt Labs, Resp Med Unit, Edinburgh, Midlothian, Scotland
来源
FEBS LETTERS | 2000年 / 476卷 / 03期
关键词
organ bath; hyperoxia; reactive oxygen species; glutathione; nitric oxide; synthase;
D O I
10.1016/S0014-5793(00)01748-8
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
Molecular oxygen (O-2) regulates the expression of a variety of genes. We hypothesized that O-2 tension may regulate iNOS expression in rat liver through the production of reactive oxygen species (ROS) and the reduction of intracellular glutathione (GSH) levels. To investigate this hypothesis, we determined the effects of hyperoxia upon iNOS induction (both at the protein and mRNA level) and the intracellular concentration of GSH in an isolated in vitro perfused rat liver preparation. To study the potential involvement of ROS in the intracellular signaling pathway linking changes in oxygen tension to gene expression, we repeated these determinations in the presence of the thiol antioxidant N-acetyl-L-cysteine (NAC). We found that 95'% O-2 tension caused a significant induction of the iNOS protein and mRNA levels paralleled by a significant fall in intracellular GSH concentration. The addition of NAC (1 mM) to the perfusate during hyperoxia blocked the induction of iNOS and restored GSH levels. These results indicate that molecular O-2 regulates the expression of iNOS in rat liver at the transcriptional level, most likely through the production of ROS and the reduction of intracellular GSH levels. (C) 2000 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:253 / 257
页数:5
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