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Main Title Biochemical Studies of Six Nitrogen-Containing Heterocycles in Rat Tissues.
Author Kitchin, K. T. ; Brown, J. L. ; Lijinsky, W. ;
CORP Author Health Effects Research Lab., Research Triangle Park, NC. ;National Cancer Inst., Frederick, MD. Frederick Cancer Research Facility.
Publisher c1989
Year Published 1989
Report Number EPA/600/J-89/398;
Stock Number PB90-245960
Additional Subjects Biochemistry ; Nitrogen heterocyclic compounds ; Liver ; Carcinogens ; Toxicology ; Leukocytes ; Lethal dosage ; Glutathione ; Esophagus ; Rats ; Reprints ; Ornithine decarboxylase ; DNA damage ; Alanine aminotransferase ; Cytochrome P-450
Library Call Number Additional Info Location Last
NTIS  PB90-245960 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 7p
Female rats were orally dosed with 1/5 the LD50 of either 1-nitrosopiperidine (a carcinogen), cyclohexylamine, piperidine, 4-carboxy-1-nitrosopiperidine, 4-cyclohexyl-1-nitrosopiperidine or 2 6-dimethyl-1-nitrosopiperidine at 21 and 4 hours before sacrifice. All five noncarcinogenic compounds had no effects on any experimental parameters examined (hepatic DNA damage, ornithine decarboxylase (ODC) activity, serum alanine aminotransferase (SGPT) activity, cytochrome P-450 and glutathione content). After administration of 40 mg/kg of 1-nitrosopiperidine, significant hepatic DNA damage and a 3- to 7-fold increase in the activity of hepatic ODC were observed. 1-Nitrosopiperidine (120 mg/kg, 3/5 LD50) caused DNA damage in rat liver and esophagus but not in leukocytes. The higher dose of 1-nitrosopiperidine also decreased hepatic cytochrome P-450 content by 37% and increased hepatic ornithine decarboxylase activity by 9-fold. As ODC is often induced by tumor-promoters, 1-nitrosopiperidine may have both promoting and initiating properties. (Copyright (c) 1989 Maxwell Pergamon Macmillan plc.)