Maternal exposure to perfluorobutane sulfonate (PFBS) during pregnancy: evidence of adverse maternal and fetoplacental effects in New Zealand White (NZW) rabbits

被引:9
|
作者
Crute, Christine E. [1 ,2 ,3 ]
Landon, Chelsea D. [4 ,5 ]
Garner, Angela [5 ]
Hall, Samantha M. [1 ,2 ,9 ]
Everitt, Jeffery, I [5 ]
Zhang, Sharon [2 ]
Blake, Bevin [6 ]
Olofsson, Didrik [7 ]
Chen, Henry
Stapleton, Heather M. [1 ,2 ]
Murphy, Susan K. [1 ,3 ]
Feng, Liping [1 ,3 ,8 ]
机构
[1] Duke Univ, Nicholas Sch Environm, Integrated Toxicol & Environm Hlth Program, Durham, NC 27710 USA
[2] Duke Univ, Nicholas Sch Environm, Durham, NC 27710 USA
[3] Duke Univ, Dept Obstet & Gynecol, Sch Med, Durham, NC 27710 USA
[4] Duke Univ, Div Lab Anim Resources, Med Ctr, Durham, NC 27710 USA
[5] Duke Univ, Sch Med, Dept Pathol, Durham, NC 27710 USA
[6] Univ North Carolina Chapel Hill, Curriculum Toxicol & Environm Med, Chapel Hill, NC 27599 USA
[7] Omiqa Bioinformat GmbH, D-14195 Berlin, Germany
[8] Duke Univ, Sch Med, Dept Obstet & Gynecol, 701 Main St, Durham, NC 27710 USA
[9] ICF, Durham, NC 27713 USA
基金
美国国家卫生研究院;
关键词
per- and polyfluoroalkyl substances (PFAS); perfluorobutanesulfonic acid (PFBS); rabbit; developmental and reproductive toxicology; placenta; birth outcomes; PULSE PRESSURE; POTASSIUM PERFLUOROBUTANESULFONATE; POLYFLUOROALKYL SUBSTANCES; PERFLUOROALKYL SUBSTANCES; PERFLUOROOCTANE SULFONATE; PLACENTAL WEIGHT; DRINKING-WATER; BIRTH-WEIGHT; ORAL GAVAGE; GROWTH;
D O I
10.1093/toxsci/kfac126
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Perfluorobutanesulfonic acid (PFBS) is a replacement for perfluorooctanesulfonic acid (PFOS) that is increasingly detected in drinking water and human serum. Higher PFBS exposure is associated with risk for preeclampsia, the leading cause of maternal and infant morbidity and mortality in the United States. This study investigated relevant maternal and fetal health outcomes after gestational exposure to PFBS in a New Zealand White rabbit model. Nulliparous female rabbits were supplied drinking water containing 0 mg/l (control), 10 mg/l (low), or 100 mg/l (high) PFBS. Maternal blood pressure, body weights, liver and kidney weights histopathology, clinical chemistry panels, and thyroid hormone levels were evaluated. Fetal endpoints evaluated at necropsy included viability, body weights, crown-rump length, and liver and kidney histopathology, whereas placenta endpoints included weight, morphology, histopathology, and full transcriptome RNA sequencing. PFBS-high dose dams exhibited significant changes in blood pressure markers, seen through increased pulse pressure and renal resistive index measures, as well as kidney histopathological changes. Fetuses from these dams showed decreased crown-rump length. Statistical analysis of placental weight via a mixed model statistical approach identified a significant interaction term between PFBS high dose and fetal sex, suggesting a sex-specific effect on placental weight. RNA sequencing identified the dysregulation of angiotensin (AGT) in PFBS high-dose placentas. These results suggest that PFBS exposure during gestation leads to adverse maternal outcomes, such as renal injury and hypertension, and fetal outcomes, including decreased growth parameters and adverse placenta function. These outcomes raise concerns about pregnant women's exposure to PFBS and pregnancy outcomes.
引用
收藏
页码:239 / 252
页数:14
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