Nrf2 the rescue: effects of the antioxidative/electrophilic response on the liver - PubMed (original) (raw)
Review
Nrf2 the rescue: effects of the antioxidative/electrophilic response on the liver
Curtis D Klaassen et al. Toxicol Appl Pharmacol. 2010.
Abstract
Nuclear factor erythroid 2-related factor 2 (Nrf2) is a transcription factor that positively regulates the basal and inducible expression of a large battery of cytoprotective genes. These gene products include proteins that catalyze reduction reactions (NAD(P)H:quinone oxidoreductase 1, Nqo1), conjugation reactions (glutathione-S-transferases, Gsts and UDP-glucuronosyltransferases, Ugts), as well as the efflux of potentially toxic xenobiotics and xenobiotic conjugates (multidrug resistance-associated proteins, Mrps). The significance of Nrf2 in the liver has been established, as livers of Nrf2-null mice are more susceptible to various oxidative/electrophilic stress-induced pathologies than wild-type mice. In contrast, both pharmacological and genetic models of hepatic Nrf2 activation are protective against oxidative/electrophilic stress. Furthermore, because certain Nrf2-target genes in the liver could affect the distribution, metabolism, and excretion of xenobiotics, the effects of Nrf2 on the kinetics of drugs and other xenobiotics should also be considered, with a special emphasis on metabolism and excretion. Therefore, this review highlights the research that has contributed to the understanding of the importance of Nrf2 in toxicodynamics and toxicokinetics, especially that which pertains to the liver.
2010 Elsevier Inc. All rights reserved.
References
- Alam J, Stewart D, Touchard C, Boinapally S, Choi AM, Cook JL. Nrf2, a Cap‘n’Collar transcription factor, regulates induction of the heme oxygenase-1 gene. J Biol Chem. 1999;274:26071–26078. - PubMed
- Alnouti Y, Klaassen CD. Regulation of sulfotransferase enzymes by prototypical microsomal enzyme inducers in mice. J Pharmacol Exp Ther. 2008;324:612–621. - PubMed
- Boberg EW, Miller EC, Miller JA, Poland A, Liem A. Strong evidence from studies with brachymorphic mice and pentachlorophenol that 1′-sulfooxysafrole is the major ultimate electrophilic and carcinogenic metabolite of 1′-hydroxysafrole in mouse liver. Cancer Res. 1983;43:5163–5173. - PubMed
- Buckley DB, Klaassen CD. Induction of mouse UDPglucuronosyltransferase mRNA expression in liver and intestine by activators of aryl-hydrocarbon receptor, constitutive androstane receptor, pregnane X receptor, peroxisome proliferator-activated receptor alpha, and nuclear factor erythroid 2-related factor 2. Drug Metab Dispos. 2009;37:847–856. - PMC - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 ES009716/ES/NIEHS NIH HHS/United States
- R01 ES013714/ES/NIEHS NIH HHS/United States
- T32 ES007079/ES/NIEHS NIH HHS/United States
- R01 ES001142/ES/NIEHS NIH HHS/United States
- R01 DK081461/DK/NIDDK NIH HHS/United States
- R01 ES009649/ES/NIEHS NIH HHS/United States
- P20 RR021940/RR/NCRR NIH HHS/United States
- DK081461/DK/NIDDK NIH HHS/United States
- R01 ES003192/ES/NIEHS NIH HHS/United States
- R01 ES008156/ES/NIEHS NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous