Dose additive maternal and offspring effects of oral maternal exposure to a mixture of three PFAS (HFPO-DA, NBP2, PFOS) during pregnancy in the Sprague-Dawley rat

• Published in: The Science of the total environment Vol. 892; p. 164609
• Main Authors: Conley, Justin M., Lambright, Christy S., Evans, Nicola, Farraj, Aimen K., Smoot, Jacob, Grindstaff, Rachel D., Hill, Donna, McCord, James, Medlock-Kakaley, Elizabeth, Dixon, Aaron, Hines, Erin, Gray, L. Earl
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 20-09-2023
• Subjects: Adult; Alkanesulfonic Acids - toxicity; Animals; Birthweight; Cumulative effects; Dose addition; Female; Fluorocarbons - toxicity; Humans; Liver; Male; Maternal Exposure - adverse effects; Pregnancy; Prenatal Exposure Delayed Effects - chemically induced; Rats; Rats, Sprague-Dawley; Relative potency factor; Thyroid; Cumulative effects; Dose addition; Liver; Birthweight; Relative potency factor; Thyroid
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2023.164609

Simultaneous exposure to multiple per- and polyfluoroalkyl substances (PFAS) is common in humans across the globe. Individual PFAS are associated with adverse health effects, yet the nature of mixture effects after exposure to two or more PFAS remains unclear. Previously we reported that oral administration of hexafluoropropylene oxide-dimer acid (HFPO-DA, or GenX), Nafion byproduct 2 (NBP2), or perfluorooctane sulfonate (PFOS) individually during pregnancy produced maternal and F1 effects. Here, we hypothesized that responses to the combined exposure to these three PFAS would be dose additive. Pregnant Sprague-Dawley rats were exposed to a fixed-ratio equipotent mixture where the top dose contained each PFAS at their ED50 for neonatal mortality (100 % dose = PFOS 3 mg/kg; NBP2 10 mg/kg; HFPO-DA 110 mg/kg), followed by a dilution series (33.3, 10, 3.3, and 1 %) and vehicle controls (0 % dose). Consistent with the single chemical studies, dams were exposed from gestation day (GD)14–18 or from GD8-postnatal day (PND2). Fetal and maternal livers on GD18 displayed multiple significantly upregulated genes associated with lipid and carbohydrate metabolism at all dose levels, while dams displayed significantly increased liver weight (≥3.3 % dose) and reduced serum thyroid hormones (≥33.3 % dose). Maternal exposure from GD8-PND2 significantly reduced pup bodyweights at birth (≥33.3 % dose) and PND2 (all doses), increased neonatal liver weights (≥3.3 % dose), increased pup mortality (≥3.3 % dose), and reduced maternal bodyweights and weight gain at the top dose. Echocardiography of adult F1 males and females identified significantly increased left ventricular anterior wall thickness (~10 % increase), whereas other cardiac morphological, functional, and transcriptomic measures were unaffected. Mixture effects in maternal and neonatal animals conformed to dose addition using a relative potency factor (RPF) analysis. Results support dose addition-based cumulative assessment approaches for estimating combined effects of PFAS co-exposure.
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•Mixture of PFOS, NBP2, and HFPO-DA produced dose additive maternal and F1 effects.•Maternal and fetal liver gene expression dominated by HFPO-DA•Effects were well-predicted using relative potency factors within a given endpoint.•RPFs varied by more than an order of magnitude across PFAS and endpoints.•Mixture induced ventricular wall thickening but there were no functional alterations.