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Sex differences in impacts of early gestational and peri-adolescent ozone exposure on lung development in rats: Implications for later life disease in humans

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Air pollution exposure during pregnancy may affect fetal growth. Fetal growth restriction (FGR) is associated with reduced lung function in children that can persist into adulthood. Using an established model of asymmetrical FGR in Long-Evans rats, this study investigated sex differences in effects of early life ozone exposure on lung development and maturation. Adverse health effects for i) gestational exposure (with impacts on primary alveolarization), ii) peri-adolescent exposure (with impacts on secondary alveolarization), and iii) cumulative exposure across both periods were evaluated. Notably, female offspring were most affected by gestational ozone exposure, likely because of impaired angiogenesis and corresponding decreases in primary alveolarization. Females had diminished lung capacity, fewer mature alveoli, and medial hypertrophy of small and large pulmonary arteries. Males, especially FGR-prone offspring, were more affected by peri-adolescent ozone exposure. Males had increased ductal areas, likely due to disrupted secondary alveolarization. Altered lung development may increase risk of developing diseases, such as pulmonary arterial hypertension or chronic obstructive pulmonary disease. Pulmonary arterial hypertension disproportionately affects women. In the United States, chronic obstructive pulmonary disease prevalence is increasing, especially in women; and prevalence for both men and women is highest in urbanized areas. This investigation underlines the importance of evaluating results separately by sex, and provides biologic plausibility for later consequences of early-life exposure to ozone, a ubiquitous urban air pollutant.

Impact/Purpose

The number of epidemiological investigations on air pollu­tant exposure during preg­nancy has been steadily increasing. With­in preg­nancy, the beginning of gestation was identified as a potentially sensitive exposure period based on associa­tions with epigenetic change in children. However, there is an urgent need to better understand and elucidate mechanisms by which exposure to air pol­lution early in life may alter lung development. To this end, we have established a rat model of fetal growth restriction induced by ozone expo­sure early in ges­ta­tion. Using this model, we report herein for the first time, sex-specific changes in rat lung devel­op­ment due to maternal ozone exposure during implantation only; changes due to peri-adolescent ozone exposure across a period of rapid body and lung growth; and combined effects of cumulative exposure across both periods. Results demonstrate the utility of this FGR model to provid­e sex-specific, biologically plausible mechanisms by which ozone exposure during critical developmental windows may differentially increase risk of pul­monary and cardio­vascular disease later in life. Additionally, this study underscores the importance of examining both sexes and in evaluating results separately by sex. Use of animal models to better simulate exposures in at-risk populations such as pregnant women or growing children are essential to defining vulnerable windows of exposure. . 

Citation

Dye, J., H. Nguyen, E. Stewart, M. Schladweiler, AND C. Miller. Sex differences in impacts of early gestational and peri-adolescent ozone exposure on lung development in rats: Implications for later life disease in humans. American Association of Pathologist, 194(9):1636-1663, (2024). [DOI: 10.1016/j.ajpath.2024.05.013]

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DOI: Sex differences in impacts of early gestational and peri-adolescent ozone exposure on lung development in rats: Implications for later life disease in humans
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Last updated on March 27, 2025
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