Literature DB >> 3385136

Involvement of glutathione in the reduction of captan-induced in vivo inhibition of monooxygenases and liver toxicity in the rat.

R R Dalvi1.   

Abstract

If given orally captan is relatively nontoxic, but it can be extremely toxic after parenteral exposure. Therefore, a single i.p. dose of captan (20 mg/kg) was given to male Sprague-Dawley rats and its effect on liver microsomal mixed function oxidases and certain serum enzymes (SDH, SGPT and SGOT) was studied. The single dose of captan caused marked depression of microsomal cytochrome P-450 and the activity of benzphetamine N-demethylase and aniline hydroxylase, and moderate elevation of the serum enzymes indicative of liver damage. However, reduced glutathione (100 mg/kg, i.p.) given prior to captan, appears to decrease the liver toxicity as measured by reduced inhibition of the microsomal enzymes and elevation of serum enzymes activity. The results suggest that glutathione and other compounds containing sulfhydryl groups may protect the subjects from captan-induced liver toxicity.

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Year:  1988        PMID: 3385136     DOI: 10.1080/03601238809372595

Source DB:  PubMed          Journal:  J Environ Sci Health B        ISSN: 0360-1234            Impact factor:   1.990


  2 in total

1.  Preliminary carcinogenic and cocarcinogenic studies on captan following topical exposure in mice.

Authors:  M Antony; Y Shukla; N K Mehrotra
Journal:  Bull Environ Contam Toxicol       Date:  1994-02       Impact factor: 2.151

2.  Comparative studies on the effect of fenbendazole on the liver and liver microsomal enzymes in goats, quail and rats.

Authors:  R R Dalvi
Journal:  Vet Res Commun       Date:  1989       Impact factor: 2.459

  2 in total

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