Literature DB >> 8831908

Determination of urinary 2-mercaptobenzothiazole (2-MBT), the main metabolite of 2-(thiocyanomethylthio)benzothiazole (TCMTB) in humans and rats.

A Manninen1, S Auriola, M Vartiainen, J Liesivuori, T Turunen, M Pasanen.   

Abstract

A method for biological monitoring of urinary 2-(thiocyanomethylthio)benzothiazole (TCMTB), a wood preservative and an industrial chemical, was developed. Three different doses of TCMTB in olive oil were given to male rats by gavage for 3 weeks. Urine was collected daily and the metabolites were analysed as thioethers by derivatization with pentafluorobenzyl-bromide by gas chromatography-mass spectrometry. The parent chemical was not detected in urine samples, but two metabolites of TCMTB were identified. 2-Mercaptobenzothiazole (2-MBT) was the main metabolite, and its excretion varied according to the dose. The second metabolite was 2-(mercaptomethylthio)benzothiazole. The amount of 2-MBT excreted in rat urine was 66 +/- 12% (SD), 51 +/- 20% and 44 +/- 9% for TCMTB doses of 15, 75 and 150 mg/kg, respectively. Two doses, 75 and 150 mg/kg, caused diuresis in rats during the 1 week of dosing. During the 3-week TCMTB treatment, rat liver microsomal CYP enzyme profile was not significantly changed. Urine samples of sawmill workers exposed to TCMTB were collected after their work shifts for exposure assessment. TCMTB could not be detected in the urine samples of exposed workers. Most concentrations of 2-MBT were below the limit of the detection, 0.12 mumol/l, the concentrations were 0.12-0.15 mumol/l only in few cases. The determination of 2-MBT in urine, when a sample is taken immediately after a work shift, is a suitable indicator of workers' exposure to TCMTB.

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Year:  1996        PMID: 8831908     DOI: 10.1007/s002040050315

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


  10 in total

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Review 2.  The human hepatic cytochromes P450 involved in drug metabolism.

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4.  Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians.

Authors:  T Shimada; H Yamazaki; M Mimura; Y Inui; F P Guengerich
Journal:  J Pharmacol Exp Ther       Date:  1994-07       Impact factor: 4.030

5.  Regioselectivity and stereoselectivity of androgen hydroxylations catalyzed by cytochrome P-450 isozymes purified from phenobarbital-induced rat liver.

Authors:  D J Waxman; A Ko; C Walsh
Journal:  J Biol Chem       Date:  1983-10-10       Impact factor: 5.157

6.  Regulation of testosterone hydroxylation by rat liver microsomal cytochrome P-450.

Authors:  A J Sonderfan; M P Arlotto; D R Dutton; S K McMillen; A Parkinson
Journal:  Arch Biochem Biophys       Date:  1987-05-15       Impact factor: 4.013

7.  Measurement of protein using bicinchoninic acid.

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Journal:  Anal Biochem       Date:  1985-10       Impact factor: 3.365

8.  Steroid hormone hydroxylase specificities of eleven cDNA-expressed human cytochrome P450s.

Authors:  D J Waxman; D P Lapenson; T Aoyama; H V Gelboin; F J Gonzalez; K Korzekwa
Journal:  Arch Biochem Biophys       Date:  1991-10       Impact factor: 4.013

9.  Ethoxy-, pentoxy- and benzyloxyphenoxazones and homologues: a series of substrates to distinguish between different induced cytochromes P-450.

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Journal:  Biochem Pharmacol       Date:  1985-09-15       Impact factor: 5.858

Review 10.  P450 enzymes. Inhibition mechanisms, genetic regulation and effects of liver disease.

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  10 in total
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1.  Assessing effects of germline exposure to environmental toxicants by high-throughput screening in C. elegans.

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