Reproductive and developmental toxicity of potassium perfluorohexanesulfonate in CD-1 mice

Chang, S; Butenhoff, JL; Parker, GA; Coder, PS; Zitzow, JD; Krisko, RM; Bjork, JA; Wallace, KB; Seed, JG

HERO ID

4409324

Reference Type

Journal Article

Year

2018

Language

English

PMID

29694846

HERO ID 4409324
In Press No
Year 2018
Title Reproductive and developmental toxicity of potassium perfluorohexanesulfonate in CD-1 mice
Authors Chang, S; Butenhoff, JL; Parker, GA; Coder, PS; Zitzow, JD; Krisko, RM; Bjork, JA; Wallace, KB; Seed, JG
Journal Reproductive Toxicology
Volume 78
Page Numbers 150-168
Abstract Potassium perfluorohexanesulfoante (K+PFHxS) was evaluated for reproductive/developmental toxicity in CD-1 mice. Up to 3 mg/kg-d K+PFHxS was administered (n = 30/sex/group) before mating, for at least 42 days in F0 males, and for F0 females, through gestation and lactation. F1 pups were directly dosed with K+PFHxS for 14 days after weaning. There was an equivocal decrease in live litter size at 1 and 3 mg/kg-d, but the pup-born-to-implant ratio was unaffected. Adaptive hepatocellular hypertrophy was observed, and in 3 mg/kg-d F0 males, it was accompanied by concomitant decreased serum cholesterol and increased alkaline phosphatase. There were no other toxicologically significant findings on reproductive parameters, hematology/clinical pathology/TSH, neurobehavioral effects, or histopathology. There were no treatment-related effects on postnatal survival, development, or onset of preputial separation or vaginal opening in F1 mice. Consistent with previous studies, our data suggest that the potency of PFHxS is much lower than PFOS in rodents.
Doi 10.1016/j.reprotox.2018.04.007
Pmid 29694846
Wosid WOS:000435227200018
Url https://search.proquest.com/docview/2031421843?accountid=171501
Is Certified Translation No
Dupe Override No
Comments Journal: Reproductive toxicology (Elmsford, N.Y.) ISSN:
Is Public Yes
Language Text English
Keyword Perfluorohexanesulfonate; PFHxS; Reproductive; Developmental; Liver; Cholesterol; Thyroid; Mice