Japanese Journal of Cancer Research · 1991 · 17 citations · 28 references
PharmacyPharmacologyToxicologyDevelopmental ToxicologyHepatotoxicologyMolecular ToxicologyCarcinogenicity Of Dietary ExposuresChemical-induced HepatotoxicityHepatic ToxicityHepatotoxicity MechanismsLiver DiseaseRodent ToxicologyCarcinogenic Hepatic EffectsGlutathione S-transferase ActivityHepatotoxic MechanismsIntraperitoneal AdministrationLiver Toxicity AssessmentLiver Toxicity Mechanisms
Effects of age on the induction of glutathione S-transferase placental form (GST-P)-positive hepatic foci in rats were examined using a medium-term liver bioassay system (for carcinogens). F344 male rats aged 6, 26 and 46 weeks were initially given a single intraperitoneal injection of diethylnitrosamine (DEN, 200 mg/kg) and, beginning 2 weeks later, received 0.02% 2-acetylaminofluorene (2-AAF), 0.05% phenobarbital (PB) or 1.3% acetaminophen (AAP) in the diet for 6 weeks. All animals were subjected to two-thirds hepatectomy 3 weeks after the DEN injection and were killed at week 8. Quantitative analysis of GST-P-positive foci revealed significantly (P less than 0.001) increased induction over control levels in terms of both numbers and areas for 2-AAF at all ages (6, 26 and 46 weeks), but especially in the 6-week-old case. In the PB- and AAP-treated groups, the respective enhancing and inhibitory influences were most pronounced in the animals aged 6 weeks, and were less marked in older rats. Thus, the response of F344 rats to the modifying effects of chemicals was age-dependent, the conclusion being drawn that young rats are more susceptible and therefore more appropriate for assessment of carcinogenic, promoting and inhibitory effects of chemicals.
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S M Hsu, Laurence Raine, Herbert Fanger · Journal of Histochemistry & Cytochemistry · 1981 · 14.3K citations · Full text
Nobuyuki Ito, Hiroyuki Tsuda, Masae Tatematsu et al. · Carcinogenesis · 1988 · 401 citations
Pharmacy, Pharmacology, Toxicology +14