Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation

Abstract Maternal exposure to environmental contaminants during pregnancy can profoundly influence the risk of developing cardiovascular disease in adult offspring. Our previous studies have demonstrated impaired cardiovascular health, microvascular reactivity, and cardiac function in fetal and youn...

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Main Authors: Sara B. Fournier, Vincent Lam, Michael J. Goedken, Laura Fabris, Phoebe A. Stapleton
Format: Article
Language:English
Published: Nature Portfolio 2021-09-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-98818-8
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author Sara B. Fournier
Vincent Lam
Michael J. Goedken
Laura Fabris
Phoebe A. Stapleton
author_facet Sara B. Fournier
Vincent Lam
Michael J. Goedken
Laura Fabris
Phoebe A. Stapleton
author_sort Sara B. Fournier
collection DOAJ
description Abstract Maternal exposure to environmental contaminants during pregnancy can profoundly influence the risk of developing cardiovascular disease in adult offspring. Our previous studies have demonstrated impaired cardiovascular health, microvascular reactivity, and cardiac function in fetal and young adult progeny after maternal inhalation of nano-sized titanium dioxide (nano-TiO2) aerosols during gestation. The present study was designed to evaluate the development of cardiovascular and metabolic diseases later in adulthood. Pregnant Sprague–Dawley rats were exposed to nano-TiO2 aerosols (~ 10 mg/m3, 134 nm median diameter) for 4 h per day, 5 days per week, beginning on gestational day (GD) 4 and ending on GD 19. Progeny were delivered in-house. Body weight was recorded weekly after birth. After 47 weeks, the body weight of exposed progeny was 9.4% greater compared with controls. Heart weight, mean arterial pressure, and plasma biomarkers of inflammation, dyslipidemia, and glycemic control were recorded at 3, 9 and 12 months of age, with no significant adaptations. While no clinical risk factors (i.e., hypertension, dyslipidemia, or systemic inflammation) emerged pertaining to the development of cardiovascular disease, we identified impaired endothelium-dependent and -independent arteriolar dysfunction and cardiac morphological alterations consistent with myocardial inflammation, degeneration, and necrosis in exposed progeny at 12 months. In conclusion, maternal inhalation of nano-TiO2 aerosols during gestation may promote the development of coronary disease in adult offspring.
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spelling doaj.art-f0fb8d62429c4deaa38b111461f5ee6c2022-12-21T23:36:57ZengNature PortfolioScientific Reports2045-23222021-09-0111111110.1038/s41598-021-98818-8Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestationSara B. Fournier0Vincent Lam1Michael J. Goedken2Laura Fabris3Phoebe A. Stapleton4Environmental and Occupational Health Sciences Institute, Rutgers UniversityDepartment of Pharmacology and Toxicology, Ernest Mario School of Pharmacy, Rutgers UniversityResearch Pathology Services, Rutgers UniversityDepartment of Material Science and Engineering, School of Engineering, Rutgers UniversityEnvironmental and Occupational Health Sciences Institute, Rutgers UniversityAbstract Maternal exposure to environmental contaminants during pregnancy can profoundly influence the risk of developing cardiovascular disease in adult offspring. Our previous studies have demonstrated impaired cardiovascular health, microvascular reactivity, and cardiac function in fetal and young adult progeny after maternal inhalation of nano-sized titanium dioxide (nano-TiO2) aerosols during gestation. The present study was designed to evaluate the development of cardiovascular and metabolic diseases later in adulthood. Pregnant Sprague–Dawley rats were exposed to nano-TiO2 aerosols (~ 10 mg/m3, 134 nm median diameter) for 4 h per day, 5 days per week, beginning on gestational day (GD) 4 and ending on GD 19. Progeny were delivered in-house. Body weight was recorded weekly after birth. After 47 weeks, the body weight of exposed progeny was 9.4% greater compared with controls. Heart weight, mean arterial pressure, and plasma biomarkers of inflammation, dyslipidemia, and glycemic control were recorded at 3, 9 and 12 months of age, with no significant adaptations. While no clinical risk factors (i.e., hypertension, dyslipidemia, or systemic inflammation) emerged pertaining to the development of cardiovascular disease, we identified impaired endothelium-dependent and -independent arteriolar dysfunction and cardiac morphological alterations consistent with myocardial inflammation, degeneration, and necrosis in exposed progeny at 12 months. In conclusion, maternal inhalation of nano-TiO2 aerosols during gestation may promote the development of coronary disease in adult offspring.https://doi.org/10.1038/s41598-021-98818-8
spellingShingle Sara B. Fournier
Vincent Lam
Michael J. Goedken
Laura Fabris
Phoebe A. Stapleton
Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
Scientific Reports
title Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
title_full Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
title_fullStr Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
title_full_unstemmed Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
title_short Development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
title_sort development of coronary dysfunction in adult progeny after maternal engineered nanomaterial inhalation during gestation
url https://doi.org/10.1038/s41598-021-98818-8
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