Hepatotoxicity of piperonyl butoxide in male F344 rats.

Male F344 rats were given 0, 0.6, 1.2 or 2.4% of piperonyl butoxide in the diet. At 1, 2, 4 or 12 weeks after the beginning of the experiment, liver and kidney weight and serum clinical parameters were determined and livers and kidneys were examined with light microscopy. From 1 or 2-12 weeks, distinct increase of liver weight, changes in serum clinical parameters for liver damage, oval cell proliferation, bile duct hyperplasia, single cell necrosis, enlarged and vacuolated hepatocytes, enlarged nuclei and anisonucleosis were seen in treated rats. From 4-12 weeks, cell infiltration, focal necrosis, multinucleated hepatocytes and prominent nucleoli of hepatocytes were seen in treated rats. At 12 weeks microgranulomas were seen in treated rats. Especially in rats of the 2.4% group at 12 weeks, severe enlargement of hepatocytes, severe enlargement of nuclei and multinucleated hepatocyte were seen, suggesting preneoplastic alteration. Relative kidney weights and serum urea nitrogen levels were increased in treated rats from 1 or 2-12 weeks and at 12 weeks, atrophy of proximal tubules, dilation of tubules, cell infiltration, fibrosis and accumulation of yellow-brown pigment in the proximal tubular cells were seen.

[1]  S. Oishi,et al.  Sub-acute toxicity of piperonyl butoxide in F344 rats. , 1992, Toxicology.

[2]  R. Renne,et al.  Carcinogenesis bioassay of technical-grade piperonyl butoxide in F344 rats. , 1979, Journal of the National Cancer Institute.

[3]  J. Goldstein,et al.  Effects of purified and technical piperonyl butoxide on drug-metabolizing enzymes and ultrastructure of rat liver. , 1973, Toxicology and applied pharmacology.

[4]  Tanaka Toyohito Effects of piperonyl butoxide on F1 generation mice. , 1992 .

[5]  M. Friedman,et al.  Stability of piperonyl butoxide. , 1970, Toxicology and applied pharmacology.

[6]  M. Friedman,et al.  Potentiation of methylmercury toxicity by piperonyl butoxide , 1978, Bulletin of environmental contamination and toxicology.

[7]  P. Dalvi,et al.  Differences in the effects of piperine and piperonyl butoxide on hepatic drug-metabolizing enzyme system in rats. , 1991, Drug and chemical toxicology.

[8]  David Salsburg,et al.  Statistics for toxicologists , 1986 .

[9]  L. Fishbein,et al.  Photolysis of pesticidal synergists. I. piperonyl butoxide , 1970, Bulletin of environmental contamination and toxicology.

[10]  S. Oishi,et al.  Reproductive and neurobehavioural effects in three-generation toxicity study of piperonyl butoxide administered to mice. , 1992, Food and Chemical Toxicology.

[11]  R. Harbison,et al.  Hepatic glutathione and hepatotoxicity: effects of cytochrome P-450 complexing compounds SKF 525-A, L-alpha acetylmethadol (LAAM), norLAAM, and piperonyl butoxide. , 1982, Biochemical pharmacology.

[12]  K. S. Khera,et al.  Assessment of the teratogenic potential of piperonyl butoxide, biphenyl, and phosalone in the rat. , 1979, Toxicology and applied pharmacology.

[13]  M. E. Kyle,et al.  The effect of mixed function oxidase induction and inhibition on salicylate-induced nephrotoxicity in male rats. , 1986, Toxicology and applied pharmacology.

[14]  S. Smith,et al.  Teratogenic evaluation of piperonyl butoxide in the rat. , 1977, Food and cosmetics toxicology.

[15]  Y. Hayashi,et al.  Lack of evidence of carcinogenicity of technical-grade piperonyl butoxide in F344 rats: selective induction of ileocaecal ulcers. , 1985, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.