» Articles » PMID: 51481

Biodegradation of Alpha-hexachlorocyclohexane. V. Characterization of the Major Urinary Metabolites

Overview
Specialty Pharmacology
Date 1975 May 6
PMID 51481
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

1. Free 2,4,5- and 2,4,6-trichlorophenol (TCP) have been identified by co-crystallization with authentic carrier as constituents of the urine of rats given 3-H-labelled alpha-hexachlorocyclohexane (alpha-HCH). The two TCP's constituted 7% and 63%, respectively, of the free phenol fraction which was found to account for less than 5% of all urinary metabolites. 2. 75% of the label contained in the urine of rats collected for four weeks after an i.p. dose of 14-C-alpha-HCH could be extracted into an organic solvent after alkaline and acid hydrolysis. The radioactive material thus extracted was examined by TLC and GLC. It is shown to consist mainly of chlorophenols and chlorothiophenols. 3. The extracts' major constituent was 2,4,6-TCP. Its amount was determined by GLC and was found to account for, on average, 45% of the total urinary metabolites. In conjunction with other evidence, this is considered to establish 2,4,6-TCP as the major product of alpha-HCH-biodegradation in the rat. 4. Chromatographic evidence is presented for 2,3,4,5-tetrachlorophenol and 2,4,5-TCP being other components of the chlorophenol fraction isolated from hydrolysed urine. 5. The amount of label associated with the chlorothiophenol fraction suggests a pathway involving endogenous thiol to be of significance in alpha-HCH-biodegradation in rats. Pretreatment with the drug itself increased the proportion of label associated with the fraction.

Citing Articles

Biodegradation of beta-hexachlorocyclohexane. Free metabolites in rat urine and organs.

Macholz R, Knoll R, Lewerenz H, Plass R Arch Toxicol. 1982; 50(1):85-8.

PMID: 6180701 DOI: 10.1007/BF00569240.


Oxidative transformation of hexachlorocyclohexane in rats and with rat liver microsomes.

Stein K, PORTIG J, KORANSKY W Naunyn Schmiedebergs Arch Pharmacol. 1977; 298(2):115-28.

PMID: 69994 DOI: 10.1007/BF00508618.


Biodegradation of alpha-hexachlorocyclohexane. VII. Resolution, purification, and characterization of an alpha-HCH dechlorinating enzyme from rat liver cytosol.

Kraus P Naunyn Schmiedebergs Arch Pharmacol. 1976; 296(1):67-72.

PMID: 64937 DOI: 10.1007/BF00498841.


Biodegradation of alpha-hexachlorocyclohexane. VI. The cechlorination of alpha-hexachlorocyclohexane by microsomes and cytosol of rat liver.

Kraus P Naunyn Schmiedebergs Arch Pharmacol. 1975; 291(1):79-87.

PMID: 53794 DOI: 10.1007/BF00510822.

References
1.
JONDORF W, Parke D, Williams R . Studies in detoxication. 66. The metabolism of halogenobenzenes: 1:2:3-, 1:2:4- and 1:3:5-trichlorobenzenes. Biochem J. 1955; 61(3):512-21. PMC: 1215820. DOI: 10.1042/bj0610512. View

2.
Noack G, PORTIG J, Wirsching M . Biodegradation of alpha-hexachlorocyclohexane. IV. The extent of degradation of single doses in vivo. Naunyn Schmiedebergs Arch Pharmacol. 1975; 288(1):57-64. DOI: 10.1007/BF00501813. View

3.
Boyland E, Chasseaud L . The role of glutathione and glutathione S-transferases in mercapturic acid biosynthesis. Adv Enzymol Relat Areas Mol Biol. 1969; 32:173-219. DOI: 10.1002/9780470122778.ch5. View

4.
Grover P, Sims P . The metabolism of gamma-2,3,4,5,6-pentachlorocyclohex-1-ene and gamma-hexachlorocyclohexane in rats. Biochem J. 1965; 96(2):521-5. PMC: 1207069. DOI: 10.1042/bj0960521. View

5.
PORTIG J, Kraus P, Sodomann S, Noack G . Biodegradation of alpha-hexachlorocyclohexane. I. Glutathione-dependent conversion to a hydrophilic metabolite by rat liver cytosol. Naunyn Schmiedebergs Arch Pharmacol. 1973; 279(2):185-98. DOI: 10.1007/BF00503982. View