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电子尼古丁传送系统与香烟相比,对支气管上皮细胞的毒性较低: Replica 项目。

Electronic nicotine delivery systems exhibit reduced bronchial epithelial cells toxicity compared to cigarette: the Replica Project.

机构信息

Department of Biomedical and Biotechnological Sciences, University of Catania, Via S. Sofia, 97, 95123, Catania, Italy.

Center of Excellence for the Acceleration of Harm Reduction (CoEHAR), University of Catania, Via S. Sofia, 97, 95123, Catania, Italy.

出版信息

Sci Rep. 2021 Dec 17;11(1):24182. doi: 10.1038/s41598-021-03310-y.


DOI:10.1038/s41598-021-03310-y
PMID:34921164
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8683499/
Abstract

Electronic nicotine delivery systems (ENDS) may reduce health risks associated with chronic exposure to smoke and their potential benefits have been the matter of intense scientific debate. We aimed to replicate three published studies on cytotoxic and inflammatory effects of cigarette smoke and ENDS aerosol in an independent multi-center ring study. We aimed to establish the reliability of results and the robustness of conclusions by replicating the authors' experimental protocols and further validating them with different techniques. Human bronchial epithelial cells (NCI-H292) were exposed to cigarette whole smoke and vapor phase and to aerosol from ENDS. We also assessed the inflammatory cytokines interleukin-6 and interleukin-8 and the remodeling mediator matrix metalloproteinase-1. We replicated cell viability results and confirmed that almost 80% of cytotoxic effects are due to volatile compounds in the vapor phase of smoke. Our findings substantiated the reduced cytotoxic effects of ENDS aerosol. However, our data on inflammatory and remodeling activity triggered by smoke differed significantly from those in the original reports. Taken together, independent data from multiple laboratories clearly demonstrated the reduced toxicity of ENDS products compared to cigarettes.

摘要

电子尼古丁传送系统(ENDS)可能降低与长期暴露于烟雾相关的健康风险,其潜在益处一直是激烈科学争论的主题。我们旨在通过独立的多中心环状研究复制三篇关于香烟烟雾和 ENDS 气溶胶细胞毒性和炎症作用的已发表研究。我们旨在通过复制作者的实验方案并进一步用不同的技术对其进行验证,来确定结果的可靠性和结论的稳健性。我们将人支气管上皮细胞(NCI-H292)暴露于香烟的全烟雾和气相以及 ENDS 的气溶胶中。我们还评估了促炎细胞因子白细胞介素-6 和白细胞介素-8 以及重塑介质基质金属蛋白酶-1。我们复制了细胞活力结果,并证实几乎 80%的细胞毒性作用是由于烟雾气相中的挥发性化合物引起的。我们的研究结果证实了 ENDS 气溶胶的细胞毒性降低。然而,我们关于烟雾引发的炎症和重塑活性的数据与原始报告中的数据有显著差异。总之,来自多个实验室的独立数据清楚地表明,与香烟相比,ENDS 产品的毒性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/3011fa00a105/41598_2021_3310_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/fb29e423a022/41598_2021_3310_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/03cd70c421de/41598_2021_3310_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/63faeaae758e/41598_2021_3310_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/88576ac01b89/41598_2021_3310_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/3a3c6ef80fb5/41598_2021_3310_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/498a0b7cbff4/41598_2021_3310_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/95b4274a1483/41598_2021_3310_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/0eb452db8006/41598_2021_3310_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/07976b136cc7/41598_2021_3310_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/133d6444a21b/41598_2021_3310_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/ebf0e32d11a7/41598_2021_3310_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/a99b6e18fd10/41598_2021_3310_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/3011fa00a105/41598_2021_3310_Fig13_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/fb29e423a022/41598_2021_3310_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/03cd70c421de/41598_2021_3310_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/63faeaae758e/41598_2021_3310_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/88576ac01b89/41598_2021_3310_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/3a3c6ef80fb5/41598_2021_3310_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/498a0b7cbff4/41598_2021_3310_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/95b4274a1483/41598_2021_3310_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/0eb452db8006/41598_2021_3310_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/07976b136cc7/41598_2021_3310_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/133d6444a21b/41598_2021_3310_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/ebf0e32d11a7/41598_2021_3310_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/a99b6e18fd10/41598_2021_3310_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0816/8683499/3011fa00a105/41598_2021_3310_Fig13_HTML.jpg

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本文引用的文献

[1]
Cigarette smoke preparations, not electronic nicotine delivery system preparations, induce features of lung disease in a 3D lung repeat-dose model.

Am J Physiol Lung Cell Mol Physiol. 2021-2-1

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Arch Toxicol. 2020-1

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Regul Toxicol Pharmacol. 2017-10-1

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Toxicol Lett. 2017-8-5

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