Effect of dietary malathion on hepatic microsomal drug-metabolizing systems of Gallus domesticus.
C Varshneya, H S Bahga, L D Sharma
Index: Toxicol. Lett. 31(2) , 107-11, (1986)
Full Text: HTML
Abstract
White leghorn cockerels were fed a diet containing 0, 400, 800 and 1600 ppm of malathion for 90 days. Malathion O,O-dimethyl S-(1,2-dicarbethoxy) ethyl phosphorodithioate) at 800 and 1600 ppm caused a significant decrease in body weights. There was a significant increase in liver/body weight ratio. A marked inhibition of aniline hydroxylation and demethylation of p-chloro N-methyl aniline was observed in the 9000 X g supernatant fraction of liver. Protein contents of liver supernatant of the treated group were significantly lower than control. Plasma half-lives of antipyrine in cockerels receiving malathion at 800 and 1600 ppm were considerably increased. Pentobarbital sleeping time was longer in malathion-treated cockerels.
Related Compounds
Related Articles:
The role of pharmacokinetics and metabolism in species sensitivity to neurotoxic agents.
1986-02-01
[Fundam. Appl. Toxicol. 6(2) , 190-207, (1986)]
2010-02-15
[Bioorg. Med. Chem. Lett. 20(4) , 1363-7, (2010)]
FT-IR, FT-Raman, NMR spectra and DFT calculations on 4-chloro-N-methylaniline.
2010-05-01
[Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 75(5) , 1523-9, (2010)]
Inhibition of hepatic drug metabolism in VX2 carcinoma-bearing rabbits.
1980-01-01
[Drug Metab. Dispos. 8(3) , 139-42, (1980)]
1990-07-01
[Xenobiotica 20(7) , 711-26, (1990)]