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Inhibition of two rat hepatic microsomal drug-metabolizing enzymes by a carcinogenic N-nitrosated pesticide: N-nitrosocarbaryl.

Abstract
N-Nitrosocarbaryl (N-methyl-1-naphthyl N-nitrosocarbamate) was intraperitoneally administered to male and female rats on four consecutive days at the following doses: 6.25 mg, 12.5 mg, 25 mg and 50 mg/kg body weight/day in olive oil solution; the controls received just the oil. In a second experiment, a daily intraperitoneal dose of 25 mg/kg of N-nitrosocarbaryl was given for 1, 2, 3 or 4 days; the animals were killed 24 h after the last treatment. The two following microsomal enzymatic activities were assayed: aniline aromatic hydroxylase and p-nitroanisole O-demethylase; the levels of cytochrome P-450, proteins and RNA were measured in the hepatic microsomal fraction. N-Nitrosocarbaryl is an inhibitor of the two investigated microsomal monooxygenases at doses of 25 and 50 mg/kg when administered on 4 consecutive days. During the daily administration, enzyme inhibition is seen in females after one day of treatment whereas cytochrome P-450 only becomes lowered after 4 days of administration. In males, no modification of this parameter is observed whereas the activities of microsomal monooxygenases are inhibited. These results suggest that N-nitrosocarbaryl could act on the active sites of the enzymes which metabolize aniline and p-nitroanisole.
AuthorsM Beraud, S Gaillard, R Derache
JournalChemico-biological interactions (Chem Biol Interact) Vol. 31 Issue 1 Pg. 103-12 (Jul 1980) ISSN: 0009-2797 [Print] Ireland
PMID6156018 (Publication Type: Journal Article)
Chemical References
  • Nitrosamines
  • Proteins
  • RNA
  • Cytochrome P-450 Enzyme System
  • nitrosocarbaryl
  • Nitroanisole O-Demethylase
  • Oxidoreductases
  • Aniline Hydroxylase
  • Aryl Hydrocarbon Hydroxylases
  • Carbaryl
Topics
  • Aniline Hydroxylase (antagonists & inhibitors)
  • Animals
  • Aryl Hydrocarbon Hydroxylases (antagonists & inhibitors)
  • Body Weight (drug effects)
  • Carbaryl (analogs & derivatives, toxicity)
  • Cytochrome P-450 Enzyme System (metabolism)
  • Female
  • Male
  • Microsomes, Liver (enzymology)
  • Nitroanisole O-Demethylase (antagonists & inhibitors)
  • Nitrosamines (toxicity)
  • Organ Size (drug effects)
  • Oxidoreductases (antagonists & inhibitors)
  • Proteins (metabolism)
  • RNA (metabolism)
  • Rats

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