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母代孕期和哺乳期暴露于聚苯乙烯微塑料改变了母鼠及其 F1 和 F2 后代的代谢稳态。

Maternal Polystyrene Microplastic Exposure during Gestation and Lactation Altered Metabolic Homeostasis in the Dams and Their F1 and F2 Offspring.

机构信息

College of Biotechnology and Bioengineering , Zhejiang University of Technology , Hangzhou 310032 , China.

出版信息

Environ Sci Technol. 2019 Sep 17;53(18):10978-10992. doi: 10.1021/acs.est.9b03191. Epub 2019 Sep 4.

DOI:10.1021/acs.est.9b03191
PMID:31448906
Abstract

Microplastics (MPs) are considered as a pollutant of marine environments and have become a global environmental problem in recent years. A number of studies have demonstrated that MPs can enter the human food chain, and MPs have even been detected in human stools. Therefore, there is increasing concern about the potential risks of MPs to human and animal health. Here, we investigated maternal polystyrene MPs exposure during gestation and lactation and evaluated the potential effects on dams and the F1 (both PND 42 and 280) and F2 (PND 42) generations. The results of transcriptome and 16S rRNA sequencing indicated that MPs caused the metabolic disorder in maternal MPs associated with gut microbiota dysbiosis and gut barrier dysfunction. Simultaneously, maternal MPs exposure also had the intergenerational effects and even caused long-term metabolic consequences in the F1 and F2 generations. In addition, in F1 (PND 42), the composition of gut microbiota did not change significantly, while the hepatic transcriptome and serum metabolite changes showed the potential risk in metabolic disorder. Then, the potential of hepatic lipid accumulation was observed in adult F1 mice (PND 280), especially in the female mice. Our results demonstrated that maternal MPs exposure during gestation and lactation increases the risk of metabolic disorder, and these results provide new insight into the potential long-term hazards of MPs.

摘要

微塑料(MPs)被认为是海洋环境的污染物,近年来已成为全球性的环境问题。许多研究表明 MPs 可以进入人类食物链,甚至在人类粪便中也检测到了 MPs。因此,人们越来越关注 MPs 对人类和动物健康的潜在风险。在这里,我们研究了孕哺期母体聚苯乙烯 MPs 暴露情况,并评估了其对母体及其 F1(PND42 和 280)和 F2(PND42)代的潜在影响。转录组和 16S rRNA 测序的结果表明, MPs 导致了与肠道微生物失调和肠道屏障功能障碍相关的母体 MPs 代谢紊乱。同时,母体 MPs 暴露也具有代际效应,甚至在 F1 和 F2 代中引起长期代谢后果。此外,在 F1(PND42)中,肠道微生物群落的组成没有明显变化,而肝转录组和血清代谢物变化显示出代谢紊乱的潜在风险。然后,在成年 F1 小鼠(PND280)中观察到肝脂质积累的潜力,尤其是在雌性小鼠中。我们的研究结果表明,孕哺期母体 MPs 暴露增加了代谢紊乱的风险,这些结果为 MPs 的潜在长期危害提供了新的见解。

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