Kim Yong Ho, Tong Haiyan, Daniels Mary, Boykin Elizabeth, Krantz Q Todd, McGee John, Hays Michael, Kovalcik Kasey, Dye Janice A, Gilmour M Ian
Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, U,S, Environmental Protection Agency, Research Triangle Park, NC, USA.
Part Fibre Toxicol. 2014 Jun 16;11:29. doi: 10.1186/1743-8977-11-29.
Emissions from a large peat fire in North Carolina in 2008 were associated with increased hospital admissions for asthma and the rate of heart failure in the exposed population. Peat fires often produce larger amounts of smoke and last longer than forest fires, however few studies have reported on their toxicity. Moreover, reliable alternatives to traditional animal toxicity testing are needed to reduce the number of animals required for hazard identification and risk assessments.
Size-fractionated particulate matter (PM; ultrafine, fine, and coarse) were obtained from the peat fire while smoldering (ENCF-1) or when nearly extinguished (ENCF-4). Extracted samples were analyzed for chemical constituents and endotoxin content. Female CD-1 mice were exposed via oropharyngeal aspiration to 100 μg/mouse, and assessed for relative changes in lung and systemic markers of injury and inflammation. At 24 h post-exposure, hearts were removed for ex vivo functional assessments and ischemic challenge. Lastly, 8 mm diameter lung slices from CD-1 mice were exposed (11 μg) ± co-treatment of PM with polymyxin B (PMB), an endotoxin-binding compound.
On an equi-mass basis, coarse ENCF-1 PM had the highest endotoxin content and elicited the greatest pro-inflammatory responses in the mice including: increases in bronchoalveolar lavage fluid protein, cytokines (IL-6, TNF-α, and MIP-2), neutrophils and intracellular reactive oxygen species (ROS) production. Exposure to fine or ultrafine particles from either period failed to elicit significant lung or systemic effects. In contrast, mice exposed to ENCF-1 ultrafine PM developed significantly decreased cardiac function and greater post-ischemia-associated myocardial infarction. Finally, similar exposures to mouse lung slices induced comparable patterns of cytokine production; and these responses were significantly attenuated by PMB.
The findings suggest that exposure to coarse PM collected during a peat fire causes greater lung inflammation in association with endotoxin and ROS, whereas the ultrafine PM preferentially affected cardiac responses. In addition, lung tissue slices were shown to be a predictive, alternative assay to assess pro-inflammatory effects of PM of differing size and composition. Importantly, these toxicological findings were consistent with the cardiopulmonary health effects noted in epidemiologic reports from exposed populations.
2008年北卡罗来纳州一场大型泥炭火灾产生的排放物与暴露人群中哮喘住院人数增加以及心力衰竭发生率上升有关。泥炭火灾通常比森林火灾产生更多的烟雾且持续时间更长,然而关于其毒性的研究报道较少。此外,需要可靠的替代传统动物毒性测试的方法,以减少危害识别和风险评估所需的动物数量。
在泥炭火灾闷烧时(ENCF - 1)或接近熄灭时(ENCF - 4)获取按粒径分级的颗粒物(PM;超细、细和粗颗粒)。对提取的样品进行化学成分和内毒素含量分析。通过口咽吸入法让雌性CD - 1小鼠暴露于100μg/只,并评估肺和全身损伤及炎症标志物的相对变化。在暴露后24小时,取出心脏进行离体功能评估和缺血挑战。最后,将来自CD - 1小鼠的直径8mm的肺切片暴露于(11μg)PM,并与内毒素结合化合物多粘菌素B(PMB)共同处理。
在等质量基础上,粗颗粒的ENCF - 1 PM内毒素含量最高,在小鼠中引发了最强烈的促炎反应,包括支气管肺泡灌洗液蛋白、细胞因子(IL - 6、TNF - α和MIP - 2)、中性粒细胞增加以及细胞内活性氧(ROS)生成。暴露于两个时期的细颗粒或超细颗粒均未引发显著的肺部或全身效应。相反,暴露于ENCF - 1超细PM的小鼠心脏功能显著下降,且缺血后相关心肌梗死更严重。最后,对小鼠肺切片进行类似暴露诱导了可比的细胞因子产生模式;并且这些反应被PMB显著减弱。
研究结果表明,暴露于泥炭火灾期间收集的粗颗粒PM会因内毒素和ROS导致更严重的肺部炎症,而超细PM则优先影响心脏反应。此外,肺组织切片被证明是一种预测性的替代检测方法,可用于评估不同大小和组成的PM的促炎作用。重要的是,这些毒理学发现与暴露人群的流行病学报告中指出的心肺健康影响一致。