Maternal Titanium Dioxide Nanomaterial Inhalation Exposure Compromises Placental Hemodynamics
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2019/03/15
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Description:The fetal consequences of gestational engineered nanomaterial (ENM) exposure are unclear. The placenta is a barrier protecting the fetus and allowing transfer of substances from the maternal circulation. The purpose of this study was to determine the effects of maternal pulmonary titanium dioxide nanoparticle (nano-TiO2) exposure on the placenta and umbilical vascular reactivity. We hypothesized that pulmonary nano-TiO2 inhalation exposure increases placental vascular resistance and impairs umbilical vascular responsiveness. Pregnant Sprague-Dawley rats were exposed via whole-body inhalation to nano-TiO2 with an aerodynamic diameter of 188 +/- 0.36 nm. On gestational day (GD) 11, rats began inhalation exposures (6 h/exposure). Daily lung deposition was 87.5 +/- 2.7 microg. Animals were exposed for 6 days for a cumulative lung burden of 525 +/- 16 microg. On GD 20, placentas, umbilical artery and vein were isolated, cannulated, and treated with acetylcholine (ACh), angiotensin II (ANGII), S-nitroso-N-acetyl-DL-penicillamine (SNAP), or calcium-free superfusate (Ca2+-free). Mean outflow pressure was measured in placental units. ACh increased outflow pressure to 53 +/- 5 mmHg in sham-controls but only to 35 +/- 4 mmHg in exposed subjects. ANGII decreased outflow pressure in placentas from exposed animals (17 +/- 7 mmHg) compared to sham-controls (31 +/- 6 mmHg). Ca2+-free superfusate yielded maximal outflow pressures in sham-control (63 +/- 5 mmHg) and exposed (30 +/- 10 mmHg) rats. Umbilical artery endothelium-dependent dilation was decreased in nano-TiO2 exposed fetuses (30 +/- 9%) compared to sham-controls (58 +/- 6%), but ANGII sensitivity was increased (-79 +/- 20% vs -36 +/- 10%). These results indicate that maternal gestational pulmonary nano-TiO2 exposure increases placental vascular resistance and impairs umbilical vascular reactivity. [Description provided by NIOSH]
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ISSN:0041-008X
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Pages in Document:51-61
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Volume:367
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NIOSHTIC Number:nn:20054789
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Citation:Toxicol Appl Pharmacol 2019 Mar; 367:51-61
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Contact Point Address:Timothy R. Nurkiewicz, Department of Physiology and Pharmacology, 64 Medical Center Drive, Robert C. Byrd Health Sciences Center, West Virginia University, Morgantown, WV 26505-9229, USA
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Email:tnurkiewicz@hsc.wvu.edu
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Federal Fiscal Year:2019
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Peer Reviewed:True
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Source Full Name:Toxicology and Applied Pharmacology
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Main Document Checksum:urn:sha-512:7fcfaeb901383dc1dd86b73cc7b86d936b5b092ed2c51cd6150b4f3761d8a168b2675d463e20f8a112575b5bf3dd4580cbcc43ff36ccd90802341b468d74b83d
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