Literature DB >> 8319644

Nephrotoxic and genotoxic N-acetyl-S-dichlorovinyl-L-cysteine is a urinary metabolite after occupational 1,1,2-trichloroethene exposure in humans: implications for the risk of trichloroethene exposure.

G Birner1, S Vamvakas, W Dekant, D Henschler.   

Abstract

Excretion of mercapturic acids in the urine is indicative of the formation of electrophiles in the metabolism of xenobiotics. The determination of these mercapturic acids thus may be a useful method to estimate the exposure. We identified the nephrotoxic and mutagenic mercapturic acids N-acetyl-S-(1,2-dichlorovinyl)-L- cysteine and N-acetyl-S-(2,2-dichlorovinyl)-L-cysteine in the urine of workers exposed to 1,1,2-trichloroethene. A method to quantify these mercapturic acids by gas chromatography-mass spectrometry-selected ion monitoring was developed and appreciable amounts (2.8-3.8 mumole/L were found in human urine samples. Because deacetylation determines notably the amount of the excreted mercapturic acids, the formation of the resulting cysteine S-conjugates was comparably measured in subcellular fractions of rodent and human kidneys; significant species differences in acylase activity were found. The formation of mutagenic and nephrotoxic metabolites during 1,1,2-trichloroethene metabolism mandates a revision of the risk assessment of trichloroethene exposure.

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Year:  1993        PMID: 8319644      PMCID: PMC1567030          DOI: 10.1289/ehp.9399281

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  6 in total

Review 1.  Bioactivation of xenobiotics by formation of toxic glutathione conjugates.

Authors:  M Koob; W Dekant
Journal:  Chem Biol Interact       Date:  1991       Impact factor: 5.192

2.  Metabolic conversion of tri- and tetrachloroethylene: formation and deactivation of genotoxic intermediates.

Authors:  W Dekant
Journal:  Dev Toxicol Environ Sci       Date:  1986

3.  Bacterial beta-lyase mediated cleavage and mutagenicity of cysteine conjugates derived from the nephrocarcinogenic alkenes trichloroethylene, tetrachloroethylene and hexachlorobutadiene.

Authors:  W Dekant; S Vamvakas; K Berthold; S Schmidt; D Wild; D Henschler
Journal:  Chem Biol Interact       Date:  1986-10-15       Impact factor: 5.192

4.  Metabolism of trichloroethene--in vivo and in vitro evidence for activation by glutathione conjugation.

Authors:  W Dekant; M Koob; D Henschler
Journal:  Chem Biol Interact       Date:  1990       Impact factor: 5.192

5.  Biochemical, histological, and ultrastructural changes in rat and mouse liver following the administration of trichloroethylene: possible relevance to species differences in hepatocarcinogenicity.

Authors:  C R Elcombe; M S Rose; I S Pratt
Journal:  Toxicol Appl Pharmacol       Date:  1985-07       Impact factor: 4.219

6.  Identification of N-acetyl(2,2-dichlorovinyl)- and N-acetyl(1,2-dichlorovinyl)-L-cysteine as two regioisomeric mercapturic acids of trichloroethylene in the rat.

Authors:  J N Commandeur; N P Vermeulen
Journal:  Chem Res Toxicol       Date:  1990 May-Jun       Impact factor: 3.739

  6 in total
  22 in total

1.  Metabolism and tissue distribution of orally administered trichloroethylene in male and female rats: identification of glutathione- and cytochrome P-450-derived metabolites in liver, kidney, blood, and urine.

Authors:  Lawrence H Lash; David A Putt; Jean C Parker
Journal:  J Toxicol Environ Health A       Date:  2006-07

Review 2.  Impact of environmental exposures on ovarian function and role of xenobiotic metabolism during ovotoxicity.

Authors:  Poulomi Bhattacharya; Aileen F Keating
Journal:  Toxicol Appl Pharmacol       Date:  2012-04-13       Impact factor: 4.219

3.  Re-assessment of the influence of polymorphisms of phase-II metabolic enzymes on renal cell cancer risk of trichloroethylene-exposed workers.

Authors:  Bernd Wiesenhütter; Silvia Selinski; Klaus Golka; Thomas Brüning; Hermann M Bolt
Journal:  Int Arch Occup Environ Health       Date:  2007-05-04       Impact factor: 3.015

4.  Increased incidence of renal cell tumours in a cohort of cardboard workers exposed to trichloroethylene.

Authors:  L J Bloemen; J Tomenson
Journal:  Arch Toxicol       Date:  1995       Impact factor: 5.153

5.  N-biotinyl-S-(1,2-dichlorovinyl)-L-cysteine sulfoxide as a potential model for S-(1,2-dichlorovinyl)-L-cysteine sulfoxide: characterization of stability and reactivity with glutathione and kidney proteins in vitro.

Authors:  Roy M Irving; Mark S Brownfield; Adnan A Elfarra
Journal:  Chem Res Toxicol       Date:  2011-10-25       Impact factor: 3.739

6.  Renal Cell Carcinomas in Vinylidene Chloride-exposed Male B6C3F1 Mice Are Characterized by Oxidative Stress and TP53 Pathway Dysregulation.

Authors:  Schantel A Hayes; Arun R Pandiri; Thai-vu T Ton; Hue-Hua L Hong; Natasha P Clayton; Keith R Shockley; Shyamal D Peddada; Kevin Gerrish; Michael Wyde; Robert C Sills; Mark J Hoenerhoff
Journal:  Toxicol Pathol       Date:  2015-12-17       Impact factor: 1.902

Review 7.  Trichloroethylene biotransformation and its role in mutagenicity, carcinogenicity and target organ toxicity.

Authors:  Lawrence H Lash; Weihsueh A Chiu; Kathryn Z Guyton; Ivan Rusyn
Journal:  Mutat Res Rev Mutat Res       Date:  2014 Oct-Dec       Impact factor: 5.657

8.  Alterations of the renal function in the isolated perfused rat kidney system after in vivo and in vitro application of S-(1,2-dichlorovinyl)-L-cysteine and S-(2,2-dichlorovinyl)-L-cysteine.

Authors:  O Ilinskaja; S Vamvakas
Journal:  Arch Toxicol       Date:  1996       Impact factor: 5.153

9.  Detection of multiple globin monoadducts and cross-links after in vitro exposure of rat erythrocytes to S-(1,2-dichlorovinyl)-L-cysteine sulfoxide and after in vivo treatment of rats with S-(1,2-dichlorovinyl)-L-cysteine sulfoxide.

Authors:  Nella Barshteyn; Adnan A Elfarra
Journal:  Chem Res Toxicol       Date:  2008-08-06       Impact factor: 3.739

10.  Increased incidence of renal cell tumors in a cohort of cardboard workers exposed to trichloroethene.

Authors:  D Henschler; S Vamvakas; M Lammert; W Dekant; B Kraus; B Thomas; K Ulm
Journal:  Arch Toxicol       Date:  1995       Impact factor: 5.153

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