IQOS对巨噬细胞活力和功能的影响

Shanon Malela, A. Scott, D. Thickett, G. Sandhar
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引用次数: 1

摘要

热不燃(HNB)装置被作为一种危害较小的传统香烟替代品出售。菲利普莫里斯公司最新的HNB设备IQOS可以产生一种无烟的烟草蒸汽,尼古丁可以通过这种蒸汽被释放出来。IQOS加热甘油浸渍的烟草棒,形成蒸汽而不是烟雾。装置文献暗示亚燃烧温度降低了有害成分的水平。迫切需要调查潜在的不良影响。目的:探讨IQOS蒸汽提取物(IVE)和香烟烟雾提取物(CSE)对THP-1巨噬细胞活力和功能的影响。方法:PMA诱导巨噬细胞向THP-1单核细胞分化24 h,静置3 d。CSE和IVE是由3支肯塔基研究卷烟/ 3根烟草棒在10 ml培养基中起泡制备的。细胞滴度法测定细胞活力。Annexin V / PI染色流式细胞术检测细胞凋亡和坏死。用Phrodo法测定吞噬能力。结果:CSE和IVE均在24小时后产生剂量依赖性的活力降低,在3% CSE和IVE刺激后显著丧失活力。3%和5%的CSE/IVE处理6小时后细胞凋亡明显增加。坏死有增加的趋势,但目前还不明显。CSE组与IVE组在细胞凋亡方面无显著差异。CSE和IVE在2%浓度时显著抑制吞噬作用,但CSE在所有浓度下的抑制作用都强于IVE。结论:CSE和IVE对THP-1巨噬细胞具有相似的毒性和抑制作用。因此,这些初步研究强调了使用IQOS设备的潜在毒性问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of IQOS on macrophage viability and function
Heat not burn (HNB) devices are being sold as a less harmful alternative to traditional cigarettes. The newest HNB device from Philip Morris, IQOS, produces a smoke free tobacco vapour through which nicotine can be delivered. IQOS heats the glycerine impregnated tobacco stick to form a vapour instead of smoke. The device literature implies the sub-combustion temperature reduces of levels of harmful components. There is an urgent need to investigate potential adverse effects. Objective: To investigate the effects of IQOS vapour extract (IVE) and cigarette smoke extract (CSE) on THP-1 macrophage viability and function. Methods: Macrophages were differentiated from THP-1 monocytes by PMA challenge for 24 hours then rested for 3 days. CSE and IVE were produced by bubbling 3 Kentucky research cigarettes / 3 tobacco sticks through 10 ml media. Viability was assessed by Cell titre aqueous assay. Apoptosis and necrosis were assessed by flow cytometry using Annexin V / PI staining. Phagocytosis was assessed by Phrodo assay. Results: Both CSE and IVE produced a dose dependent reduction in viability after 24 hours, with significant loss of viability after 3% CSE and IVE challenge. Apoptosis was significantly increased after 6 hours with 3% and 5% CSE/IVE. There was a trend towards increased necrosis however this was not significant currently. There was no significant difference in apoptosis between CSE and IVE. Phagocytosis was significantly inhibited by CSE and IVE at 2% however CSE showed greater inhibition than IVE at all concentrations. Conclusion: Exposure to CSE and IVE produced similar toxic and inhibitory effects on THP-1 macrophages. As such these preliminary studies highlight potential toxicity concerns regarding use of IQOS devices.
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