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纳米塑料和苯并[a]芘诱导氧化损伤的复合效应及机制。

Compound effect and mechanism of oxidative damage induced by nanoplastics and benzo [a] pyrene.

机构信息

School of Environmental Science and Engineering, Shandong University, China-America CRC for Environment & Health, Shandong Province, 72# Jimo Binhai Road, Qingdao, Shandong 266237, PR China.

College of Chemistry, Chemical Engineering and Material Science, Zaozhuang University, Zaozhuang, Shandong Province 277160, PR China.

出版信息

J Hazard Mater. 2023 Oct 15;460:132513. doi: 10.1016/j.jhazmat.2023.132513. Epub 2023 Sep 9.

DOI:10.1016/j.jhazmat.2023.132513
PMID:37708649
Abstract

Nanoplastics and polycyclic aromatic hydrocarbons (PAHs) are ubiquitous in soil environments. In order to objectively evaluate the toxic interaction between polystyrene nanoplastics (PS NPs) and benzo [a] pyrene (BaP), oxidative damage at the level of earthworm cells and biomacromolecules was investigated by experiments combined with molecular dynamics simulation. Studies on cells reveal that PS NPs and BaP had synergistic toxicity when it came to causing oxidative stress. Cellular reactive oxygen species (ROS) levels under combined pollutant exposure were 24% and 19% higher, respectively than when PS NPs and BaP were exposed alone (compared to the blank group). In addition, BaP and PS NPs inhibited the ability of CAT to decompose HO by affecting the structure of the proximal amino acid Tyr 357 in the active center of CAT, which exacerbated oxidative stress to a certain extent. Therefore, the synergistic toxic effect of BaP and PS NPs is due to the mutual complement of the two to the induction of protein structural looseness, and the strengthening of the stability of the conjugate (CAT-BaP-PS) under the weak interaction. This work provides a new perspective and approach on how to talk about the toxicity of combined pollutants.

摘要

纳米塑料和多环芳烃(PAHs)在土壤环境中普遍存在。为了客观评估聚苯乙烯纳米塑料(PS NPs)和苯并[a]芘(BaP)之间的毒性相互作用,通过实验结合分子动力学模拟研究了其对蚯蚓细胞和生物大分子的氧化损伤。细胞研究表明,PS NPs 和 BaP 在引起氧化应激方面具有协同毒性。与单独暴露于 PS NPs 和 BaP 相比,联合污染物暴露下细胞内活性氧(ROS)水平分别升高了 24%和 19%(与空白组相比)。此外,BaP 和 PS NPs 通过影响 CAT 活性中心近端氨基酸 Tyr 357 的结构,抑制了 CAT 分解 HO 的能力,这在一定程度上加剧了氧化应激。因此,BaP 和 PS NPs 的协同毒性作用是由于两者相互补充,导致蛋白质结构松弛,并在弱相互作用下增强了结合物(CAT-BaP-PS)的稳定性。这项工作为探讨复合污染物的毒性提供了一个新的视角和方法。

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