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现代和旧技术木材燃烧产生的颗粒物排放会在体外诱导出具有明显时间依赖性的毒理学反应模式。

Particulate emissions from modern and old technology wood combustion induce distinct time-dependent patterns of toxicological responses in vitro.

机构信息

University of Eastern Finland, Kuopio, Finland.

University of Eastern Finland, Kuopio, Finland.

出版信息

Toxicol In Vitro. 2017 Oct;44:164-171. doi: 10.1016/j.tiv.2017.07.005. Epub 2017 Jul 12.

Abstract

Toxicological characterisation of combustion emissions in vitro are often conducted with macrophage cell lines, and the majority of these experiments are based on responses measured at 24h after the exposure. The aim of this study was to investigate how significant role time course plays on toxicological endpoints that are commonly measured in vitro. The RAW264.7 macrophage cell line was exposed to PM samples (150μg/ml) from biomass combustion devices representing old and modern combustion technologies for 2, 4, 8, 12, 24 and 32h. After the exposure, cellular metabolic activity, cell membrane integrity, cellular DNA content, DNA damage and production of inflammatory markers were assessed. The present study revealed major differences in the time courses of the responses, statistical differences between the studied samples mostly limiting to differences between modern and old technology samples. Early stage responses consisted of disturbances in metabolic activity and cell membrane integrity. Middle time points revealed increases in chemokine production, whereas late-phase responses exhibited mostly increased DNA-damage, decreased membrane integrity and apoptotic activity. Altogether, these results implicate that the time point of measurement has to be considered carefully, when the toxicity of emission particles is characterised in in vitro study set-ups.

摘要

体外燃烧排放物的毒理学特征通常使用巨噬细胞细胞系进行研究,并且这些实验中的大多数都基于暴露后 24 小时测量的反应。本研究旨在探讨在体外常用的毒理学终点上,时间过程起着多么重要的作用。将 RAW264.7 巨噬细胞系暴露于代表旧和现代燃烧技术的生物质燃烧设备的 PM 样品(150μg/ml)中 2、4、8、12、24 和 32 小时。暴露后,评估细胞代谢活性、细胞膜完整性、细胞 DNA 含量、DNA 损伤和炎症标志物的产生。本研究揭示了反应时间过程的主要差异,研究样本之间的统计学差异主要限于现代技术样本和旧技术样本之间的差异。早期阶段的反应包括代谢活性和细胞膜完整性的紊乱。中期时间点显示趋化因子产生增加,而晚期反应则表现为 DNA 损伤增加、细胞膜完整性和凋亡活性降低。总之,这些结果表明,在体外研究中,当表征排放颗粒的毒性时,必须仔细考虑测量的时间点。

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