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孕期接触臭氧和卵清蛋白诱导的子代哮喘:敏感窗口识别。

Exposure to O during pregnancy and offspring asthma induced by OVA: Sensitive window identification.

机构信息

Department of Occupational and Environmental Health, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.

Department of Occupational and Environmental Health, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.

出版信息

Environ Pollut. 2021 Feb 1;270:116297. doi: 10.1016/j.envpol.2020.116297. Epub 2020 Dec 13.

Abstract

BACKGROUND

Evidence proved that gestational ozone (O) exposure can increase the risk of neonatal adverse respiratory outcomes, but offspring asthma is unclear.

OBJECTIVE

This study aimed to investigate whether gestational O exposure could exacerbate offspring asthma, and to research the differences in effects of O exposure at different gestational periods on offspring asthma.

METHODS

The pregnant ICR mice were randomly grouped and were administered O (air as control) at gestational day (GD) 1-6, 7-12, and 13-18, respectively. The pups aged 2-4 weeks were treated with ovalbumin (OVA) to establish a model of early life asthma. Asthma characteristics such as pulmonary inflammation, goblet cell proliferation, airway remodeling, OVA-specific immunoglobulin (Ig) E secretion and cytokines were examined.

RESULTS

OVA sensitization and challenge successfully induced asthma in offspring. Compared with the air control, pulmonary inflammation infiltration, mucous secretion, the concentration of OVA-specific IgE, the level of tumor necrosis factor (TNF)-α, and T helper (Th) 2-skewed response were significantly exacerbated when O exposure at GD13-18 following inhaling OVA, while pulmonary inflammatory infiltration, mucus secretion, and Th2-skewed response were not significantly changed when O exposure at both GD1-6 and GD7-12. What's more, the above indicators in asthmatic offspring due to O exposure at GD13-18 were more severe than at GD1-6 and GD7-12. Interestingly, the signs of asthma only appeared in the offspring after OVA inhalation. When offspring were not treated with OVA, the prenatal O exposure alone did not lead to asthmatic reactions in offspring. In addition, O exposure at GD13-18 markedly increased the number of neutrophils and macrophages in Bronchoalveolar Lavage Fluid (BALF) of asthmatic offspring, and significantly exacerbated Th2 immune imbalance in asthmatic offspring, but had no effect on Th17 immune imbalance.

CONCLUSION

Exposure to O during pregnancy aggravated asthma in offspring, in which the third trimester is the most sensitive window.

摘要

背景

有证据表明,妊娠期臭氧(O)暴露会增加新生儿不良呼吸结局的风险,但对后代哮喘的影响尚不清楚。

目的

本研究旨在探讨妊娠期 O 暴露是否会加重后代哮喘,并研究不同妊娠期 O 暴露对后代哮喘的影响差异。

方法

将怀孕的 ICR 小鼠随机分组,并分别在妊娠第 1-6、7-12 和 13-18 天给予 O(空气为对照)。2-4 周龄的幼鼠用卵清蛋白(OVA)处理,建立早期生命哮喘模型。检测肺部炎症、杯状细胞增殖、气道重塑、OVA 特异性免疫球蛋白(Ig)E 分泌和细胞因子等哮喘特征。

结果

OVA 致敏和激发成功地诱导了后代的哮喘。与空气对照组相比,当在吸入 OVA 后进行 GD13-18 的 O 暴露时,肺部炎症浸润、黏液分泌、OVA 特异性 IgE 浓度、肿瘤坏死因子(TNF)-α 水平和 Th2 偏向反应显著加重,而在 GD1-6 和 GD7-12 进行 O 暴露时,肺部炎症浸润、黏液分泌和 Th2 偏向反应没有显著变化。更重要的是,由于 GD13-18 的 O 暴露而导致哮喘的后代的上述指标比 GD1-6 和 GD7-12 更严重。有趣的是,只有在 OVA 吸入后,哮喘的迹象才会出现在后代中。当后代未接受 OVA 处理时,单独的产前 O 暴露不会导致后代发生哮喘反应。此外,GD13-18 的 O 暴露明显增加了哮喘后代支气管肺泡灌洗液(BALF)中的中性粒细胞和巨噬细胞数量,并显著加重了哮喘后代的 Th2 免疫失衡,但对 Th17 免疫失衡没有影响。

结论

妊娠期暴露于 O 会加重后代的哮喘,其中孕晚期是最敏感的窗口。

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