Environmental Toxicology · 2008 · 21 citations · 18 references
PharmacyToxicologyDevelopmental ToxicologyReproductive ToxicologyToxicodynamicsDevelopmental NeurotoxicityDevelopmental ToxicityReproductive ToxicityRodent ToxicologyAnimal Weight GainDevelopmental Neurotoxicity In AnimalsDevelopmental Reproductive ToxicityPerinatal Reproductive ToxicityReproductive Development ToxicityRodent Developmental Toxicity Models
Rats were treated by gavage once daily with 2,4-dinitrophenol (DNP) at 0 (control), 3, 10, or 30 mg/kg bw. Males were dosed for 46 days, beginning 14 days before mating, and females were dosed for 40-47 days, from 14 days before mating to day 3 of lactation. No deaths were observed in males and females of any group. A significant decrease in body weight gain and significant increase in liver weight were found in males and females at 30 mg/kg bw/day. The number of live pups on postnatal days (PNDs) 0 and 4, live birth index, and body weight of live male and female pups on PNDs 0 and 1 were significantly lowered at 30 mg/kg bw/day. External and internal examinations of pups revealed no increased incidence of malformations in DNP-treated groups. On the basis of these findings, we concluded that DNP has general and reproductive/developmental toxicity, but not teratogenicity, under the present conditions. The NOAEL of DNP is considered to be 10 mg/kg bw/day in rats.
18
Abnormalities induced in cultured rat embryos by hyperthermia
D. L. Cockroft, D. A. T. New · Teratology · 1978 · 102 citations