Repeated dose and reproductive/developmental toxicity of perfluorooctadecanoic acid in rats

• Published in: Journal of toxicological sciences 2012/02/01, Vol.37(1), pp.63-79
• Main Authors: Hirata-Koizumi, Mutsuko, Fujii, Sakiko, Furukawa, Masatoshi, Ono, Atsushi, Hirose, Akihiko
• Format: Article
• Language: English
• Subjects: Anemia - chemically induced; Animals; Birth weight; Blood Proteins - analysis; Body weight gain; Decanoic Acids - toxicity; Environmental Pollutants - toxicity; Erythrocytes; Female; Fluorocarbons - toxicity; Gestation; Hematocrit; Hemoglobin; Hypertrophy; Lactation; Liver; Liver - drug effects; Liver - pathology; Male; Maternal-Fetal Exchange; Necrosis; No-Observed-Adverse-Effect Level; Organ Size - drug effects; Pancreas; Pancreas - drug effects; Pancreas - pathology; Perfluorooctadecanoic acid; Pregnancy; Rat; Rats; Repeated dose toxicity; Reproduction - drug effects; Reproductive and developmental toxicity; Screening test; Sex; thromboplastin; Toxicity; Zymogen granules
• ISSN: 0388-1350; 1880-3989
• DOI: 10.2131/jts.37.63

Male and female rats were given perfluorooctadecanoic acid (PFOdA) by gavage at 40, 200 or 1,000 mg/kg/day, and each female was mated with a male in the same dose group after 14-day administration. Males were dosed for 42 days and females were dosed throughout the gestation period until day 5 of lactation. One female given 1,000 mg/kg/day was euthanized on day 18 of gestation due to a moribund condition; however, no other treatment-related clinical signs of toxicity were observed. Body weights fell at 1,000 mg/kg/day from day 28 through the administration period in males and throughout gestation and lactation in females. Red blood cell count, hemoglobin level and hematocrit were decreased at 200 and 1,000 mg/kg/day in males and activated partial thromboplastin time was prolonged at 1,000 mg/kg/ day in females. Histopathological examination revealed hepatic changes, such as centrilobular hypertrophy and necrosis, in males given 200 and 1,000 mg/kg/day and in females given 1,000 mg/kg/day. Pancreatic zymogen granule was decreased in both sexes at 1,000 mg/kg/day. As for reproductive and developmental toxicity, there were decreases in the number of corpora lutea, implantation, total number of pups born and the number of live pups on postnatal days 0 and 4 at 1,000 mg/kg/day. At this dose, birth weights of pups were decreased and postnatal body weight gain was inhibited. Based on these findings, the NOAEL of PFOdA was considered to be 40 mg/kg/day for repeated dose toxicity and 200 mg/kg/day for reproductive/developmental toxicity.