Literature DB >> 9851677

Species differences in the glutathione transferase GSTT1-1 activity towards the model substrates methyl chloride and dichloromethane in liver and kidney.

R Thier1, F A Wiebel, A Hinkel, A Burger, T Brüning, K Morgenroth, T Senge, M Wilhelm, T G Schulz.   

Abstract

Glutathione transferase (GST) GSTT1-1 is involved in the biotransformation of several chemicals widely used in industry, such as butadiene and dichloro methane DCM. The polymorphic hGSTT1-1 may well play a role in the development of kidney tumours after high and long-term occupational exposure against trichloroethylene. Although several studies have investigated the association of this polymorphism with malignant diseases little is known about its enzyme activity in potential extrahepatic target tissues. The known theta-specific substrates methyl chloride (MC) dichloromethane and 1,2-epoxy-3-(p-nitrophenoxy)propane (EPNP) were used to assay GSTT1-1 activity in liver and kidney of rats, mice, hamsters and humans differentiating the three phenotypes (non-conjugators, low conjugators, high conjugators) seen in humans. In addition GSTT1-1 activity towards MC and DCM was determined in human erythrocytes. No GSTT1-1 activity was found in any tissue of non-conjugators (NC). In all organs high conjugators (HC) showed twofold higher activity towards MC and DCM than low conjugators (LC). The activity in human samples towards EPNP was too close to the detection limit to differentiate between the three conjugator phenotypes. GSTT1-1 activity towards MC was two to seven-times higher in liver cytosol than in kidney cytosol. The relation for MC between species was identical in both organs: mouse > HC > rat > LC > hamster > NC. In rats, mice and hamsters GSTT1-1 activity in liver cytosol towards DCM was also two to seven-times higher than in the kidney cytosol. In humans this activity was twice as high in kidney cytosol than in liver cytosol. The relation between species was mouse > rat > HC > LC > hamster > NC for liver, but mouse > HC > LC/rat > hamster/NC for kidney cytosol. The importance to heed the specific environment at potential target sites in risk assessment is emphasized by these results.

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Year:  1998        PMID: 9851677     DOI: 10.1007/s002040050552

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  7 in total

1.  Genetic variants in carcinogen-metabolizing enzymes, cigarette smoking and pancreatic cancer risk.

Authors:  Ji-Hyun Jang; Michelle Cotterchio; Ayelet Borgida; Steven Gallinger; Sean P Cleary
Journal:  Carcinogenesis       Date:  2012-02-02       Impact factor: 4.944

2.  PharmGKB summary: very important pharmacogene information for GSTT1.

Authors:  Caroline F Thorn; Yuan Ji; Richard M Weinshilboum; Russ B Altman; Teri E Klein
Journal:  Pharmacogenet Genomics       Date:  2012-08       Impact factor: 2.089

3.  Residue 234 in glutathione transferase T1-1 plays a pivotal role in the catalytic activity and the selectivity against alternative substrates.

Authors:  Abeer Shokeer; Anna-Karin Larsson; Bengt Mannervik
Journal:  Biochem J       Date:  2005-05-15       Impact factor: 3.857

4.  DNA polymerase I is essential for growth of Methylobacterium dichloromethanicum DM4 with dichloromethane.

Authors:  M F Kayser; M T Stumpp; S Vuilleumier
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

5.  GSTM1 and GSTT1 Null Genotype Polymorphisms and Susceptibility to Arsenic Poisoning: a Meta-analysis.

Authors:  Baiming Jin; Siyuan Wan; Michael Boah; Jie Yang; Wenjing Ma; Man Lv; Haonan Li; Kewei Wang
Journal:  Biol Trace Elem Res       Date:  2020-08-08       Impact factor: 3.738

Review 6.  Insights from epidemiology into dichloromethane and cancer risk.

Authors:  Glinda S Cooper; Cheryl Siegel Scott; Ambuja S Bale
Journal:  Int J Environ Res Public Health       Date:  2011-08-18       Impact factor: 3.390

7.  Spontaneous Production of Glutathione-Conjugated Forms of 1,2-Dichloropropane: Comparative Study on Metabolic Activation Processes of Dihaloalkanes Associated with Occupational Cholangiocarcinoma.

Authors:  Yu Toyoda; Tappei Takada; Hiroshi Suzuki
Journal:  Oxid Med Cell Longev       Date:  2017-05-07       Impact factor: 6.543

  7 in total

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