» Articles » PMID: 34588535

Development of Coronary Dysfunction in Adult Progeny After Maternal Engineered Nanomaterial Inhalation During Gestation

Overview
Journal Sci Rep
Specialty Science
Date 2021 Sep 30
PMID 34588535
Citations 1
Authors
Affiliations
Soon will be listed here.
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-TiO) 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-TiO aerosols (~ 10 mg/m, 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-TiO aerosols during gestation may promote the development of coronary disease in adult offspring.

Citing Articles

In Utero Nano-Titanium Dioxide Exposure Results in Sexually Dimorphic Weight Gain and Cardiovascular Function in Offspring.

Hunter R, Gluth T, Meadows E, Nett R, Nist V, Bowdridge E Cardiovasc Toxicol. 2025; 25(3):354-364.

PMID: 39838185 PMC: 11885329. DOI: 10.1007/s12012-025-09960-y.


Single pulmonary nanopolystyrene exposure in late-stage pregnancy dysregulates maternal and fetal cardiovascular function.

Cary C, Fournier S, Adams S, Wang X, Yurkow E, Stapleton P Toxicol Sci. 2024; 199(1):149-159.

PMID: 38366927 PMC: 11057520. DOI: 10.1093/toxsci/kfae019.

References
1.
Niu Y, DesMarais T, Tong Z, Yao Y, Costa M . Oxidative stress alters global histone modification and DNA methylation. Free Radic Biol Med. 2015; 82:22-8. PMC: 4464695. DOI: 10.1016/j.freeradbiomed.2015.01.028. View

2.
Stapleton P, Minarchick V, Cumpston A, McKinney W, Chen B, Sager T . Impairment of coronary arteriolar endothelium-dependent dilation after multi-walled carbon nanotube inhalation: a time-course study. Int J Mol Sci. 2012; 13(11):13781-803. PMC: 3509550. DOI: 10.3390/ijms131113781. View

3.
Masoud R, Bizouarn T, Trepout S, Wien F, Baciou L, Marco S . Titanium Dioxide Nanoparticles Increase Superoxide Anion Production by Acting on NADPH Oxidase. PLoS One. 2015; 10(12):e0144829. PMC: 4699827. DOI: 10.1371/journal.pone.0144829. View

4.
Engler-Chiurazzi E, Stapleton P, Stalnaker J, Ren X, Hu H, Nurkiewicz T . Impacts of prenatal nanomaterial exposure on male adult Sprague-Dawley rat behavior and cognition. J Toxicol Environ Health A. 2016; 79(11):447-52. PMC: 4899177. DOI: 10.1080/15287394.2016.1164101. View

5.
Fournier S, Kallontzi S, Fabris L, Love C, Stapleton P . Effect of Gestational Age on Maternofetal Vascular Function Following Single Maternal Engineered Nanoparticle Exposure. Cardiovasc Toxicol. 2019; 19(4):321-333. PMC: 6642065. DOI: 10.1007/s12012-019-09505-0. View