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      Evaluation of Maternal, Embryo, and Placental Effects in CD-1 Mice following Gestational Exposure to Perfluorooctanoic Acid (PFOA) or Hexafluoropropylene Oxide Dimer Acid (HFPO-DA or GenX)

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          Abstract

          Background:

          Perfluorooctanoic acid (PFOA) is a poly- and perfluoroalkyl substance (PFAS) associated with adverse pregnancy outcomes in mice and humans, but little is known regarding one of its replacements, hexafluoropropylene oxide dimer acid (HFPO-DA, referred to here as GenX), both of which have been reported as contaminants in drinking water.

          Objectives:

          We compared the toxicity of PFOA and GenX in pregnant mice and their developing embryo–placenta units, with a specific focus on the placenta as a hypothesized target.

          Methods:

          Pregnant CD-1 mice were exposed daily to PFOA (0, 1, or 5 mg / kg ) or GenX (0, 2, or 10 mg / kg ) via oral gavage from embryonic day (E) 1.5 to 11.5 or 17.5 to evaluate exposure effects on the dam and embryo–placenta unit. Gestational weight gain (GWG), maternal clinical chemistry, maternal liver histopathology, placental histopathology, embryo weight, placental weight, internal chemical dosimetry, and placental thyroid hormone levels were determined.

          Results:

          Exposure to GenX or PFOA resulted in increased GWG, with increase in weight most prominent and of shortest latency with 10 mg / kg / d GenX exposure. Embryo weight was significantly lower after exposure to 5 mg / kg / d PFOA (9.4% decrease relative to controls). Effect sizes were similar for higher doses ( 5 mg / kg / d PFOA and 10 mg / kg / d GenX) and lower doses ( 1 mg / kg / d PFOA and 2 mg / kg / d GenX), including higher maternal liver weights, changes in liver histopathology, higher placental weights and embryo–placenta weight ratios, and greater incidence of placental abnormalities relative to controls. Histopathological features in placentas suggested that PFOA and GenX may exhibit divergent mechanisms of toxicity in the embryo–placenta unit, whereas PFOA- and GenX-exposed livers shared a similar constellation of adverse pathological features.

          Conclusions:

          Gestational exposure to GenX recapitulated many documented effects of PFOA in CD-1 mice, regardless of its much shorter reported half-life; however, adverse effects toward the placenta appear to have compound-specific signatures. https://doi.org/10.1289/EHP6233

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                Author and article information

                Journal
                Environ Health Perspect
                Environ. Health Perspect
                EHP
                Environmental Health Perspectives
                Environmental Health Perspectives
                0091-6765
                1552-9924
                13 February 2020
                February 2020
                : 128
                : 2
                : 027006
                Affiliations
                [1 ]Curriculum in Toxicology and Environmental Medicine, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina, USA
                [2 ]Division of the National Toxicology Program (DNTP), NTP Laboratory, National Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH) , Research Triangle Park, North Carolina, USA
                [3 ]Nicholas School of the Environment, Duke University , Durham, North Carolina, USA
                [4 ]Cellular and Molecular Pathology Branch, National Toxicology Program (NTP), National Institute of Environmental Health Sciences , Research Triangle Park, North Carolina, USA
                [5 ]Exposure Methods and Measurements Division, National Exposure Research Laboratory, Office of Research and Development (ORD), U.S. EPA , Research Triangle Park, North Carolina, USA
                Author notes
                Address correspondence to Suzanne E. Fenton, 111 T.W. Alexander Drive, MD E1-08, Research Triangle Park, NC 27709. Telephone: (984) 287-4182. Email: fentonse@ 123456niehs.nih.gov
                Article
                EHP6233
                10.1289/EHP6233
                7064328
                32074459
                b1b5e46a-3851-4ddb-a478-02ed265eee75

                EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted.

                History
                : 17 September 2019
                : 22 January 2020
                : 23 January 2020
                Categories
                Research

                Public health
                Public health

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