Differential role of ethanol and acetaldehyde in the induction of oxidative stress in HEP G2 cells: Effect on transcription factors AP-1 and NF-κB
- 1 December 1999
- journal article
- research article
- Published by Wolters Kluwer Health in Hepatology
- Vol. 30 (6) , 1473-1480
- https://doi.org/10.1002/hep.510300623
Abstract
The oxidative metabolism of ethanol by the cytochrome P450 2E1 (CYP2E1) has been recognized to contribute to the ethanol-induced deleterious effects through the induction of oxidative stress. This study compared the effect of ethanol and acetaldehyde in the induction of oxidative stress and activation of transcription factors nuclear factor-κB (NF-κB) and activating protein 1 (AP-1) in HepG2 cells, which do not express CYP2E1, and HepG2 cells transfected with CYP2E1 (E47 cells). Neither ethanol (80 mmol/L) nor acetaldehyde (25-200 μmol/L) caused oxidative stress in HepG2 cells, an effect that was independent of blocking reduced glutathione (GSH) synthesis with buthionine-l -sulfoximine (BSO). However, BSO preincubation caused an overproduction of peroxides and activation of NF-κB and AP-1 in E47 cells even in the absence of ethanol. Furthermore, the incubation of E47 cells with ethanol (80 mmol/L for up to 5 days) depleted cellular GSH stores in both cytosol and mitochondria, reflecting the induction of oxidative stress. Ethanol activated NF-κB and AP-1 in E47 cells, an effect that was prevented by 4-methylpyrazole, potentiated by cyanamide, and attenuated by trolox C. Interestingly, however, despite the inability of acetaldehyde to induce oxidative stress in HepG2, acetaldehyde activated NF-κB and AP-1; in contrast, ethanol failed to activate these transcription factors in HepG2. Thus, our findings indicate that activation of NF-κB and AP-1 by ethanol and acetaldehyde occurs through distinct mechanisms. CYP2E1 is indispensable in the induction of oxidative stress from ethanol, whereas the activation of NF-κB and AP-1 by acetaldehyde is independent of oxidative stress.Keywords
Funding Information
- U.S. National Institute of Alcohol Abuse and Alcoholism
- Alcohol Center (P50 AA11999)
- Dirección General Política Científica y Técnica (PM 95-0185)
- Plan Nacional de I+D grants SAF (97-0087-001, SAF-98-0009, SAF 99-0138)
- Fondo Investigaciones Sanitarias grant FISS (95-0485)
- Europharma
This publication has 30 references indexed in Scilit:
- Transcriptional regulation of the heavy subunit chain of γ‐glutamylcysteine synthetase by ionizing radiationFEBS Letters, 1998
- Antibodies to tumor necrosis factor alfa attenuate hepatic necrosis and inflammation caused by chronic exposure to ethanol in the ratHepatology, 1997
- Tumor Necrosis Factor Increases Hepatocellular Glutathione by Transcriptional Regulation of the Heavy Subunit Chain of γ-Glutamylcysteine SynthetaseJournal of Biological Chemistry, 1997
- Direct Effect of Ceramide on the Mitochondrial Electron Transport Chain Leads to Generation of Reactive Oxygen SpeciesJournal of Biological Chemistry, 1997
- Oxidative Stress–Mediated Apoptosis of Hepatocytes Exposed to Acute Ethanol IntoxicationHepatology, 1997
- Hepatotoxicity induced by iron overload and alcohol: Studies on the role of chelatable iron, cytochrome P450 2E1 and lipid peroxidationJournal of Hepatology, 1996
- Ethanol Cytotoxicity to a Transfected HepG2 Cell Line Expressing Human Cytochrome P4502E1Journal of Biological Chemistry, 1996
- Evidence That the Rat Hepatic Mitochondrial Carrier Is Distinct from the Sinusoidal and Canalicular Transporters for Reduced GlutathioneJournal of Biological Chemistry, 1995
- Stable expression of human cytochrome P4502E1 in HepG2 cells: Characterization of catalytic activities and production of reactive oxygen intermediatesBiochemistry, 1993
- Immunohistochemical demonstration of acetaldehyde-modified epitopes in human liver after alcohol consumption.Journal of Clinical Investigation, 1991