Literature DB >> 22118226

Cytochrome P450-mediated metabolism and DNA binding of 2-amino-1,7-dimethylimidazo[4,5-g]quinoxaline and its carcinogenic isomer 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline in mice.

Robert J Turesky1, Erin E Bessette, Deborah Dunbar, Rosa G Liberman, Paul L Skipper.   

Abstract

2-Amino-1,7-dimethylimidazo[4,5-g]quinoxaline (n class="Chemical">MeIgQx) is a recently discovered heterocyclic aromatic amine (HAA) that is formed during the cooking of meats. MeIgQx is an isomer of 2-amino-3,8-dimethylmidazo[4,5-f]quinoxaline (MeIQx), a rodent carcinogen and possible human carcinogen that also occurs in cooked meats. MeIgQx is a bacterial mutagen, but knowledge about its metabolism and carcinogenic potential is lacking. Metabolism studies on MeIgQx and MeIQx were conducted with human and mouse liver microsomes, and recombinant human P450s. DNA binding studies were also investigated in mice to ascertain the genotoxic potential of MeIgQx in comparison to MeIQx. Both HAAs underwent comparable rates of N-oxidation to form genotoxic N-hydroxylated metabolites with mouse liver microsomes (0.2-0.3 nmol/min/mg protein). The rate of N-oxidation of MeIQx was 4-fold greater than the rate of N-oxidation of MeIgQx with human liver microsomes (1.7 vs 0.4 nmol/min/mg protein). The rate of N-oxidation, by recombinant human P450 1A2, was comparable for both substrates (6 pmol/min/pmol P450 1A2). MeIgQx also underwent N-oxidation by human P450s 1A1 and 1B1 at appreciable rates, whereas MeIQx was poorly metabolized by these P450s. The potential of MeIgQx and MeIQx to form DNA adducts was assessed in female C57BL/6 mice given [(14)C]-MeIgQx (10 μCi, 9.68 mg/kg body wt) or [(14)C]-MeIQx (10 μCi, 2.13 mg/kg body wt). DNA adduct formation in the liver, pancreas, and colorectum was measured by accelerator mass spectrometry at 4, 24, or 48 h post-treatment. Variable levels of adducts were detected in all organs. The adduct levels were similar for both HAAs, when adjusted for dose, and ranged from 1 to 600 adducts per 10(7) nucleotides per mg/kg dose. Thus, MeIgQx undergoes metabolic activation and binds to DNA at levels that are comparable to MeIQx. Given the high amounts of MeIgQx formed in cooked meats, further investigations are warranted to assess the carcinogenic potential of this HAA.

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Year:  2011        PMID: 22118226      PMCID: PMC3531872          DOI: 10.1021/tx2004536

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  46 in total

Review 1.  Metabolic activation and covalent binding to nucleic acids of carcinogenic heterocyclic amines from cooked foods and amino acid pyrolysates.

Authors:  R Kato; Y Yamazoe
Journal:  Jpn J Cancer Res       Date:  1987-04

2.  Successful use of short-term tests for academic purposes: their use in identification of new environmental carcinogens with possible risk for humans.

Authors:  T Sugimura
Journal:  Mutat Res       Date:  1988 May-Aug       Impact factor: 2.433

3.  Isolation of the glucuronic acid conjugate of n-hydroxy-4-aminobiphenyl from dog urine and its mutagenic activity.

Authors:  J L Radomski; W L Hearn; T Radomski; H Moreno; W E Scott
Journal:  Cancer Res       Date:  1977-06       Impact factor: 12.701

Review 4.  Human extrahepatic cytochromes P450: function in xenobiotic metabolism and tissue-selective chemical toxicity in the respiratory and gastrointestinal tracts.

Authors:  Xinxin Ding; Laurence S Kaminsky
Journal:  Annu Rev Pharmacol Toxicol       Date:  2002-01-10       Impact factor: 13.820

5.  Rapid biomonitoring of heterocyclic aromatic amines in human urine by tandem solvent solid phase extraction liquid chromatography electrospray ionization mass spectrometry.

Authors:  Ricky D Holland; Jason Taylor; Laura Schoenbachler; Richard C Jones; James P Freeman; Dwight W Miller; Brian G Lake; Nigel J Gooderham; Robert J Turesky
Journal:  Chem Res Toxicol       Date:  2004-08       Impact factor: 3.739

Review 6.  Metabolic activation of mutagenic heterocyclic aromatic amines from protein pyrolysates.

Authors:  R Kato
Journal:  Crit Rev Toxicol       Date:  1986       Impact factor: 5.635

7.  Mechanisms of action of carcinogenic aromatic amines: an investigation using mutagenesis in bacteria.

Authors:  J D Scribner; S R Fisk; N K Scribner
Journal:  Chem Biol Interact       Date:  1979-06       Impact factor: 5.192

8.  An interface for direct analysis of (14)c in nonvolatile samples by accelerator mass spectrometry.

Authors:  Rosa G Liberman; Steven R Tannenbaum; Barbara J Hughey; Ruth E Shefer; Robert E Klinkowstein; Chandra Prakash; Shawn P Harriman; Paul L Skipper
Journal:  Anal Chem       Date:  2004-01-15       Impact factor: 6.986

Review 9.  In vivo covalent binding of organic chemicals to DNA as a quantitative indicator in the process of chemical carcinogenesis.

Authors:  W K Lutz
Journal:  Mutat Res       Date:  1979-12       Impact factor: 2.433

10.  Metabolic activation of a protein pyrolysate promutagen 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline by rat liver microsomes and purified cytochrome P-450.

Authors:  Y Yamazoe; M Abu-Zeid; S Manabe; S Toyama; R Kato
Journal:  Carcinogenesis       Date:  1988-01       Impact factor: 4.944

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  3 in total

1.  Disposition of the Dietary Mutagen 2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline in Healthy and Pancreatic Cancer Compromised Humans.

Authors:  Michael A Malfatti; Edward A Kuhn; Kenneth W Turteltaub; Selwyn M Vickers; Eric H Jensen; Lori Strayer; Kristin E Anderson
Journal:  Chem Res Toxicol       Date:  2016-03-08       Impact factor: 3.739

2.  Ameliorative effects of supplemental folinic acid on Lamotrigine-induced fetal malformations in the mouse.

Authors:  Y M Abdulrazzaq; M Shafiullah; J Kochyil; R Padmanabhan; S M A Bastaki
Journal:  Mol Cell Biochem       Date:  2018-01-23       Impact factor: 3.396

3.  Caffeine Cytochrome P450 1A2 Metabolic Phenotype Does Not Predict the Metabolism of Heterocyclic Aromatic Amines in Humans.

Authors:  Robert J Turesky; Kami K White; Lynne R Wilkens; Loïc Le Marchand
Journal:  Chem Res Toxicol       Date:  2015-08-06       Impact factor: 3.739

  3 in total

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