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由卡车行驶促进的 PM 导致的亚毒性事件及其在 A549 人肺细胞中的表没食子儿茶素没食子酸酯的拮抗作用。

Sub-toxic events induced by truck speed-facilitated PM and its counteraction by epigallocatechin-3-gallate in A549 human lung cells.

机构信息

Institute of Environmental and Occupational Health Sciences, National Yang Ming Chiao Tung University, Taipei, 112, Taiwan, ROC.

Division of Basic Chinese Medicine, National Research Institute of Chinese Medicine, 155-1, Li-Nong Street, Sec. 2, Taipei, 112, Taiwan, ROC.

出版信息

Sci Rep. 2022 Sep 2;12(1):15004. doi: 10.1038/s41598-022-18918-x.

DOI:10.1038/s41598-022-18918-x
PMID:36056034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9440210/
Abstract

To distinguish the influences of fuel type and truck speed on chemical composition and sub-toxic effects of particulates (PM) from engine emissions, biomarkers-interleukin-6 (IL-6), cytochrome P450 (CYP) 1A1, heme oxygenase (HO)-1, and NADPH-quinone oxidoreductase (NQO)-1-were studied in A549 human lung cells. Fuel type and truck speed preferentially affected the quantity and ion/polycyclic aromatic hydrocarbon (PAH) composition of PM, respectively. Under idling operation, phenanthrene was the most abundant PAH. At high speed, more than 50% of the PAHs had high molecular weight (HMW), of which benzo[a]pyrene (B[a]P), benzo[ghi]perylene (B[ghi]P), and indeno[1,2,3-cd]pyrene (I[cd]P) were the main PAHs. B[a]P, B[ghi]P, and I[cd]P caused potent induction of IL-6, CYP1A1, and NQO-1, whereas phenanthrene mildly induced CYP1A1. Based on the PAH-mediated induction, the predicted increases in biomarkers were positively correlated with the measured increases. HMW-PAHs contribute to the biomarker induction by PM, at high speed, which was reduced by co-exposure to epigallocatechin-3-gallate.

摘要

为了区分燃料类型和卡车速度对颗粒物(PM)化学成分和亚毒性影响的影响,来自发动机排放的生物标志物——白细胞介素-6(IL-6)、细胞色素 P450(CYP)1A1、血红素加氧酶(HO)-1 和 NADPH-醌氧化还原酶(NQO)-1,在 A549 人肺细胞中进行了研究。燃料类型和卡车速度分别优先影响 PM 的数量和离子/多环芳烃(PAH)组成。在怠速运行时,菲是最丰富的 PAH。在高速时,超过 50%的 PAHs 具有高分子量(HMW),其中苯并[a]芘(B[a]P)、苯并[ghi]苝(B[ghi]P)和茚并[1,2,3-cd]芘(I[cd]P)是主要的 PAHs。B[a]P、B[ghi]P 和 I[cd]P 引起强烈的 IL-6、CYP1A1 和 NQO-1 诱导,而菲轻度诱导 CYP1A1。基于 PAH 介导的诱导,预测生物标志物的增加与测量增加呈正相关。HMW-PAH 在高速时通过 PM 导致生物标志物的诱导,而表没食子儿茶素没食子酸酯(EGCG)的共暴露则降低了诱导作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/f68a6ceb4c8a/41598_2022_18918_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/836a0ac57740/41598_2022_18918_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/0afed926dd18/41598_2022_18918_Fig4_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/7b5110b8b7cb/41598_2022_18918_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/f68a6ceb4c8a/41598_2022_18918_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/836a0ac57740/41598_2022_18918_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/cef90c9b59e9/41598_2022_18918_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/176ef8a81a51/41598_2022_18918_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/0afed926dd18/41598_2022_18918_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/14be72b21d1a/41598_2022_18918_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/7b5110b8b7cb/41598_2022_18918_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7be/9440210/f68a6ceb4c8a/41598_2022_18918_Fig7_HTML.jpg

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