Literature DB >> 7717850

Dose and route dependency of metabolism and toxicity of chloroform in ethanol-treated rats.

P Y Wang1, T Kaneko, H Tsukada, A Sato.   

Abstract

The effects of a single dose of ethanol on the metabolism and toxicity of chloroform administered to rats per os (p.o.), intraperitoneally (i.p.), or by inhalation (inh) at different doses were investigated. Rats that had been given either ethanol (2 g/kg) or vehicle (water) alone at 4 p.m. on the previous day were challenged with chloroform at 10 a.m. p.o. (0.01, 0.2, or 0.4 g/kg), i.p. (0, 0.1, 0.2, or 0.4 g/kg), or inh (for 6 h each at 0, 50, 100, or 500 ppm). The ethanol treatment, which had no influence on the intake of food and water, increased chloroform metabolism in vitro about 1.5-fold with no significant influence on liver glutathione content. The treatment had a dose-dependent effect on the metabolism and toxicity of chloroform, and the effect differed depending on the route of administration. Compared at the same dose level, the area under the curve (AUC) of blood chloroform concentration was invariably smaller following p.o. than i.p. administration. In accordance with this, chloroform administered p.o. caused more deleterious hepatic damage than the same amount of chloroform administered i.p. Although ethanol treatment had no significant influence on the AUC at any dose by any route of administration, the toxicity of p.o.-administered chloroform was significantly higher in ethanol-treated rats than in control rats at a dose as low as 0.1 g/kg, whereas no significant difference was observed in toxicity between both groups of rats at such a low dose administered i.p.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7717850     DOI: 10.1007/s002040050131

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


  22 in total

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Authors:  E L Docks; G Krishna
Journal:  Exp Mol Pathol       Date:  1976-02       Impact factor: 3.362

5.  Chloroform toxicity in mice: correlation of renal and hepatic necrosis with covalent binding of metabolites to tissue macromolecules.

Authors:  K F Ilett; W D Reid; I G Sipes; G Krishna
Journal:  Exp Mol Pathol       Date:  1973-10       Impact factor: 3.362

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Authors:  L R Pohl; B Bhooshan; N F Whittaker; G Krishna
Journal:  Biochem Biophys Res Commun       Date:  1977-12-07       Impact factor: 3.575

7.  Ethanol-, fasting-, and acetone-inducible cytochromes P-450 in rat liver: regulation and characteristics of enzymes belonging to the IIB and IIE gene subfamilies.

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Journal:  Biochemistry       Date:  1988-03-22       Impact factor: 3.162

8.  Enhanced metabolism of volatile hydrocarbons in rat liver following food deprivation, restricted carbohydrate intake, and administration of ethanol, phenobarbital, polychlorinated biphenyl and 3-methylcholanthrene: a comparative study.

Authors:  A Sato; T Nakajima
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9.  Enzymes induced by ethanol differently affect the pharmacokinetics of trichloroethylene and 1,1,1-trichloroethane.

Authors:  T Kaneko; P Y Wang; A Sato
Journal:  Occup Environ Med       Date:  1994-02       Impact factor: 4.402

Review 10.  The effect of environmental factors on the pharmacokinetic behaviour of organic solvent vapours.

Authors:  A Sato
Journal:  Ann Occup Hyg       Date:  1991-10
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  1 in total

1.  Within- and between-subject variations in pharmacokinetic parameters of ethanol by analysis of breath, venous blood and urine.

Authors:  A Norberg; J Gabrielsson; A W Jones; R G Hahn
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  1 in total

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