Literature DB >> 7037176

Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin and phenobarbital on the occurrence and distribution of four cytochrome P-450 isozymes in rabbit kidney, lung, and liver.

J H Dees, B S Masters, U Muller-Eberhard, E F Johnson.   

Abstract

The effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and of phenobarbital (PB) on the distribution and occurrence of four cytochrome P-450 isozymes, Forms 2, 3, 4, and 6, in the kidney, lung, and liver of adult male rabbits was investigated using immunofluorescence. In the kidney, Forms 2 and 3 were localized in the proximal tubules of both untreated and PB-treated animals, while antibodies to Forms 4 and 6 showed weak to negative staining. In TCDD-pretreated animals, Forms 4 and 6 appeared in the renal endothelium, in addition to staining the proximal tubular epithelium intensely. Form 2 was the only isoenzyme of those studied found to be present in the lungs of normal and PB-pretreated rabbits; it was also present in lungs of TCDD-pretreated rabbits. Form 3 was not detected in any of the rabbit lungs examined. Forms 4 and 6, while not apparent in the lungs of normal or PB-treated animals, were found in the lungs of TCDD-treated animals and also appeared in the endothelium of the pulmonary arteries and veins. All forms tested were present in control liver. The staining for Form 2 was intense in the livers of PB-pretreated animals, as was the staining for Forms 4 and 6 in the livers of TCDD-pretreated animals. Our results indicate that, while PB altered the intensity of staining for Form 2 in the liver and kidney, TCDD altered both the staining intensity and distribution of the isozymes in kidney, lung, and liver, producing, for example, a localization of Forms 4 and 6 in the endothelium of both the kidney and lung which was not seen in either untreated or PB-pretreated rabbits.

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Year:  1982        PMID: 7037176

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  6 in total

1.  Regulation of arachidonic acid metabolism by cytochrome P-450 in rabbit kidney.

Authors:  M L Schwartzman; N G Abraham; M A Carroll; R D Levere; J C McGiff
Journal:  Biochem J       Date:  1986-08-15       Impact factor: 3.857

2.  An understanding of the role of enzyme localization of the liver on metabolite kinetics: a computer simulation.

Authors:  K S Pang; R N Stillwell
Journal:  J Pharmacokinet Biopharm       Date:  1983-10

3.  Induction of cytochrome CYPIA1 and formation of toxic metabolites of benzo[a]pyrene by rat aorta: a possible role in atherogenesis.

Authors:  M J Thirman; J H Albrecht; M A Krueger; R R Erickson; D L Cherwitz; S S Park; H V Gelboin; J L Holtzman
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-07       Impact factor: 11.205

Review 4.  The renal cytochrome P-450 arachidonic acid system.

Authors:  M Laniado-Schwartzman; N G Abraham
Journal:  Pediatr Nephrol       Date:  1992-09       Impact factor: 3.714

Review 5.  Role of cytochrome P-450 and related enzymes in the pulmonary metabolism of xenobiotics.

Authors:  R M Philpot; B R Smith
Journal:  Environ Health Perspect       Date:  1984-04       Impact factor: 9.031

6.  Urinary D-glucaric acid excretion in the Seveso area, polluted by tetrachloro-dibenzo-p-dioxin (TCDD): five years of experience.

Authors:  G Idéo; G Bellati; A Bellobuono; L Bissanti
Journal:  Environ Health Perspect       Date:  1985-05       Impact factor: 9.031

  6 in total

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