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非靶向脂质组学揭示了体内长期暴露于聚苯乙烯微塑料引起的肝脂质特征。

Untargeted lipidomics uncover hepatic lipid signatures induced by long-term exposure to polystyrene microplastics in vivo.

机构信息

Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China.

Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China.

出版信息

Toxicol Lett. 2024 Oct;400:49-57. doi: 10.1016/j.toxlet.2024.07.914. Epub 2024 Jul 30.

DOI:10.1016/j.toxlet.2024.07.914
PMID:39084329
Abstract

OBJECTIVE

This study evaluated the effects of long-term polystyrene microplastics (PS-MPs) exposure on hepatic lipid metabolism in vivo by lipidomics.

RESULTS

H&E staining showed long-term PS-MPs exposure could trigger the hepatic inflammatory cell infiltration and hepatic steatosis in SD rats, indicating long-term PS-MPs exposure caused hepatoxicity. Lipidomics revealed that the concentrations of 8 lipid metabolites in the liver were altered after exposure to PS-MPs for both 6 and 12 months, namely LdMePE (16:0), LPC (18:1), LPC (18:2), LPC (20:4), PC (17:0_20:4), PC (18:2_22:6), PC (22:6_13:0) and SM (d18:1_24:0), which were all statistically different from the control groups detected at both time points after PS-MPs exposure, suggesting the mainly metabolic pathway was glycerolipid metabolism.

CONCLUSION

This study showed chronic exposure to PS-MPs could cause hepatotoxicity and induce hepatic lipidomics alterations in vivo, which could provide an essential clue for the safety assessment of PS-MPs.

摘要

目的

本研究通过脂质组学评估长期聚苯乙烯微塑料(PS-MPs)暴露对体内肝脂质代谢的影响。

结果

H&E 染色显示,长期 PS-MPs 暴露可引发 SD 大鼠肝炎性细胞浸润和肝脂肪变性,表明长期 PS-MPs 暴露可导致肝毒性。脂质组学分析显示,暴露于 PS-MPs 6 个月和 12 个月后,肝脏中 8 种脂质代谢物的浓度发生改变,即 LdMePE(16:0)、LPC(18:1)、LPC(18:2)、LPC(20:4)、PC(17:0_20:4)、PC(18:2_22:6)、PC(22:6_13:0)和 SM(d18:1_24:0),与暴露 PS-MPs 后两个时间点的对照组相比,这些代谢物均有统计学差异,表明主要的代谢途径是甘油磷脂代谢。

结论

本研究表明,慢性暴露于 PS-MPs 可导致肝毒性,并在体内诱导肝脂质组学改变,为 PS-MPs 的安全性评估提供了重要线索。

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Toxicol Lett. 2024 Oct;400:49-57. doi: 10.1016/j.toxlet.2024.07.914. Epub 2024 Jul 30.
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