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)

被引:168
作者
Blake, Bevin E. [1 ,2 ]
Cope, Harlie A. [2 ]
Hall, Samantha M. [3 ]
Keys, Robert D. [4 ]
Mahler, Beth W. [4 ]
McCord, James [5 ]
Scott, Brittany [4 ]
Stapleton, Heather M. [3 ]
Strynar, Mark J. [5 ]
Elmore, Susan A. [4 ]
Fenton, Suzanne E. [2 ]
机构
[1] Univ N Carolina, Curriculum Toxicol & Environm Med, Chapel Hill, NC 27515 USA
[2] NIEHS, DNTP, NTP Lab, NIH, POB 12233, Res Triangle Pk, NC 27709 USA
[3] Duke Univ, Nicholas Sch Environm, Durham, NC 27708 USA
[4] NIEHS, Cellular & Mol Pathol Branch, NTP, NIH, POB 12233, Res Triangle Pk, NC 27709 USA
[5] US EPA, Exposure Methods & Measurements Div, Natl Exposure Res Lab, ORD, Res Triangle Pk, NC 27711 USA
关键词
EVIDENCE-BASED MEDICINE; DRINKING-WATER CONTAMINANTS; PERFLUOROALKYL SUBSTANCES; THYROID-HORMONES; SULFONATE PFOS; PREGNANT-WOMEN; LACTATING MICE; MAMMARY-GLAND; FETAL-GROWTH; SERUM-LEVELS;
D O I
10.1289/EHP6233
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
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, hexalluoropropylene 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.
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页数:17
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