Literature DB >> 3350844

Biochemical effects of methyl chloride in relation to its tumorigenicity.

R Jäger1, H Peter, W Sterzel, H M Bolt.   

Abstract

The biochemical effects of methyl chloride were investigated in tissues of F-344 rats and B6C3F1 mice (both sexes). Activities of GST were 2-3 times higher in livers of male B6C3F1 mice, compared with those of female mice, and with rats of both sexes. In kidneys GST activities of (male) mice were about 7 times lower than those found in livers. The activity of FDH was higher in livers of mice (both sexes) than in those of rats. No obvious sex difference was found in livers of rats and mice with respect to FDH. In kidneys, however, (minor) differences in FDH activities occurred between male and female B6C3F1 mice (4.7 vs. 3.1 nmol/min per mg). Sex differences of FDH activity in kidneys were not observed in F-344 rats. The microsomal transformation (by cytochrome P-450) of methyl chloride and S-methyl-L-cysteine to formaldehyde in tissues of B6C3F1 mice occurred preferentially in the liver. More formaldehyde was produced in liver microsomes of male, compared to those of female mice. Kidney microsomes metabolized methyl chloride to formaldehyde much less than liver microsomes. After a single exposure of mice of both sexes to 1000 ppm methyl chloride no elevation in formaldehyde concentrations was observed in livers and kidneys ex vivo. The determination of DNA lesions, using the alkaline elution technique, revealed no DNA-protein crosslinks in kidneys of male B6C3F1 mice after exposure to methyl chloride (1000 ppm, 6 h day-1, 4 days) and gave only minor evidence of single-strand breaks. Lipid peroxidation (production of TBA reactive material), induced by single exposure to methyl chloride (1000 ppm, 6 h), was very pronounced in livers of male and female mice. Smaller increases in peroxidation were observed in the kidneys of exposed mice. The theory that renal tumors observed in male mice after chronic exposure of the test animals to high (1000 ppm) concentrations of methyl chloride, are evoked by intermediates and in situ produced formaldehyde is proven unlikely by our results.

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Year:  1988        PMID: 3350844     DOI: 10.1007/bf00390487

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  18 in total

1.  Fractionation of DNA from mammalian cells by alkaline elution.

Authors:  K W Kohn; L C Erickson; R A Ewig; C A Friedman
Journal:  Biochemistry       Date:  1976-10-19       Impact factor: 3.162

2.  Glutathione S-transferases. The first enzymatic step in mercapturic acid formation.

Authors:  W H Habig; M J Pabst; W B Jakoby
Journal:  J Biol Chem       Date:  1974-11-25       Impact factor: 5.157

3.  Association of inhaled [14C]methyl chloride with macromolecules from various rat tissues.

Authors:  D J Kornbrust; J S Bus; G Doerjer; J A Swenberg
Journal:  Toxicol Appl Pharmacol       Date:  1982-08       Impact factor: 4.219

4.  Metabolism of methyl chloride to formate in rats.

Authors:  D J Kornbrust; J S Bus
Journal:  Toxicol Appl Pharmacol       Date:  1982-08       Impact factor: 4.219

5.  Determination of formaldehyde in biological tissues by gas chromatography/mass spectrometry.

Authors:  H D Heck; E L White; M Casanova-Schmitz
Journal:  Biomed Mass Spectrom       Date:  1982-08

6.  DNA-protein cross-linking by chemical carcinogens in mammalian cells.

Authors:  A J Fornace; J B Little
Journal:  Cancer Res       Date:  1979-03       Impact factor: 12.701

7.  Evaluation of the alkaline elution/rat hepatocyte assay as a predictor of carcinogenic/mutagenic potential.

Authors:  J F Sina; C L Bean; G R Dysart; V I Taylor; M O Bradley
Journal:  Mutat Res       Date:  1983-08       Impact factor: 2.433

8.  Glutathione depletion by methyl chloride and association with lipid peroxidation in mice and rats.

Authors:  D J Kornbrust; J S Bus
Journal:  Toxicol Appl Pharmacol       Date:  1984-03-15       Impact factor: 4.219

9.  Formaldehyde damage to DNA and inhibition of DNA repair in human bronchial cells.

Authors:  R C Grafstrom; A J Fornace; H Autrup; J F Lechner; C C Harris
Journal:  Science       Date:  1983-04-08       Impact factor: 47.728

10.  DNA-binding assay of methyl chloride.

Authors:  H Peter; R J Laib; H Ottenwälder; H Topp; N Rupprich; H M Bolt
Journal:  Arch Toxicol       Date:  1985-06       Impact factor: 5.153

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  2 in total

1.  Metabolism of methyl chloride by human erythrocytes.

Authors:  H Peter; S Deutschmann; C Reichel; E Hallier
Journal:  Arch Toxicol       Date:  1989       Impact factor: 5.153

2.  Formation and repair of DNA lesions in kidneys of male mice after acute exposure to methyl chloride.

Authors:  C Ristau; H M Bolt; R R Vangala
Journal:  Arch Toxicol       Date:  1990       Impact factor: 5.153

  2 in total

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