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ToxSci Advance Access published online on May 28, 2008

Toxicological Sciences, doi:10.1093/toxsci/kfn099
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Published by Oxford University Press 2008.

Effects of perfluorobutyrate exposure during pregnancy in the mouse

Kaberi P. Das1, Brian E. Grey1, Robert D. Zehr1, Carmen R. Wood1, John L. Butenhoff2, Shu-Ching Chang2, David J. Ehresman2, Yu-Mei Tan3 and Christopher Lau1

1 Reproductive Toxicology Division, National Health and Environmental Effects Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC 2 Medical Department, 3M Corporation, St. Paul, MN 3 The Hamner Institutes for Health Sciences, Research Triangle Park, NC

Send correspondence and galley proofs to: Dr. Christopher Lau, Mail Drop 67, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, FAX: (919) 541-4017. E-mail: lau.christopher{at}epa.gov

Received February 14, 2008; revision received April 17, 2008; accepted May 16, 2008


   Abstract

Perfluorobutyrate (PFBA) is a perfluoroalkyl acid (PFAA) found in the environment. Previous studies have indicated developmental toxicity of PFAAs (perfluorooctane sulfonate (PFOS) and perfluorooctanoate (PFOA)); the current study examines that of PFBA. PFBA/NH4+ was given to timed-pregnant CD-1 mice by oral gavage daily from gestational day (GD) 1-17 at 35, 175 or 350 mg/kg (chosen to approximate the developmentally toxic doses of PFOA); controls received water. At GD 18, serum levels of PFBA were 3.8, 4.4 and 2.5 µg/mL, respectively, in the three treated groups. PFBA did not significantly affect maternal weight gain, number of implantations, fetal viability, fetus weight, or incidence of fetal malformations. Incidence of full-litter loss was significantly greater in the 350 mg/kg group, and maternal liver weights were significantly increased in the 175 and 350 mg/kg groups. In contrast to PFOA and PFOS, PFBA exposure during pregnancy did not adversely affect neonatal survival or postnatal growth. Liver enlargement was detected in the PFBA-exposed pups on postnatal day (PD) 1, but not by PD 10. Expression of selected hepatic genes in PFBA-exposed pups at PD 1 did not reveal any significant changes from controls. A significant delay in eye-opening in offspring was detected in all three PFBA groups, and slight delays in the onset of puberty were noted in the 175 and 350 mg/kg groups. These data suggest that exposure to PFBA during pregnancy in the mouse did not produce developmental toxicity comparable to that observed with PFOA, in part, due to rapid elimination of the chemical.

Key Words: perfluorobutyrate; mouse; pregnancy; developmental toxicity.


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