Pulmonary toxicity of micro- and nano polyethylene particles following intratracheal instillation in rats.

IF 10.6 1区 医学 Q1 TOXICOLOGY
Hyoung-Yun Han, Seonae Hwangbo, Eun-Jung Park, Se-Myo Park, Mi-Sun Choi, Jung-Hwa Oh, Mi-Jin Yang, Wonkyun Jung, Minjeong Kwak, Tae Geol Lee, Flemming R Cassee, Quan Lu, Seokjoo Yoon
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引用次数: 0

Abstract

Background: Micro- and nano-sized polyethylene plastics (PE-MPs and PE-NPs) are emerging as potential risk factors for pulmonary disease and risk assessment. Currently, their is no direct evidence suggests this appreciable health risk extends to humans. Furthermore, the toxicological evaluation of PE-MPs and PE-NPs is insufficient to support their safe use.

Methods: This study was aimed to characterize the toxicity of PE-MPs and PE-NPs after 13 weeks of intratracheal instillation in Sprague-Dawley (SD) rats and to assess the reversibility of any effects during a 4-week recovery period. Exposure levels for PE-MPs and PE-NPs were set at 0, 40, 80, and 120 μg per rat once a week.

Results: The results indicated that the treatment administration resulted in observable lung tissue alterations. Inflammatory cells were present in the perivascular and peribronchiolar regions in both sexes at ≥ 40 μg per rat in the PE-MPs and PE-NPs-treated groups, indicating a biological response that can turn into toxicity. Additionally, thickened alveolar ducts and alveolar epithelial hyperplasia were noted in males at 120 μg per rat PE-MPs, in males at ≥ 80 μg per rat PE-NPs, and in females at ≥ 40 μg per rat PE-MPs and PE-NPs-treated groups. Interestingly, when instilled repeatedly with both sizes of polyethylene particles, IL-1β and TNF-α secretion was significantly more enhanced in female rats compared to male rats. At the same time, the pulmonary level of IL-6 increased more clearly in male rats than in female rats. The pulmonary level of C-reactive protein, a marker for acute inflammation, was increased in all treated groups.

Conclusion: These findings suggest that the lowest-observed-adverse-effect level (LOAEL) for PE-MPs and PE-NPs based on repeated exposures is below 40 μg per rat for both sexes. However, the toxicological data for PE-MPs and PE-NPs remain insufficient to confirm their safety, and further research is necessary to evaluate their potential risks to human health.

大鼠气管内灌注微、纳米聚乙烯颗粒的肺毒性。
背景:微和纳米聚乙烯塑料(PE-MPs和PE-NPs)正在成为肺部疾病和风险评估的潜在危险因素。目前,没有直接证据表明这种明显的健康风险延伸到人类。此外,PE-MPs和PE-NPs的毒理学评价不足以支持其安全使用。方法:本研究旨在描述PE-MPs和PE-NPs在SD大鼠气管内灌注13周后的毒性,并在4周的恢复期评估任何影响的可逆性。PE-MPs和PE-NPs的暴露水平分别为0、40、80和120 μg /只大鼠,每周一次。结果:给药后肺组织明显改变。在PE-MPs和pe - nps处理组中,两性血管周围和细支气管周围区域均存在炎症细胞,每只大鼠≥40 μg,表明生物反应可转化为毒性。此外,PE-MPs≥120 μg /只大鼠、PE-NPs≥80 μg /只大鼠、PE-MPs≥40 μg /只大鼠、PE-NPs≥40 μg /只大鼠的雄性、PE-MPs和PE-NPs处理组的肺泡管增厚、肺泡上皮增生。有趣的是,当反复灌注两种大小的聚乙烯颗粒时,雌性大鼠的IL-1β和TNF-α分泌明显高于雄性大鼠。同时,肺中IL-6水平在雄性大鼠较雌性大鼠明显升高。所有治疗组的肺c反应蛋白水平(急性炎症的标志)均升高。结论:上述结果提示,PE-MPs和PE-NPs的最低观察不良反应水平(LOAEL)在每只大鼠中均低于40 μg。然而,PE-MPs和PE-NPs的毒理学数据仍不足以证实其安全性,需要进一步研究以评估其对人类健康的潜在风险。
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来源期刊
CiteScore
15.90
自引率
4.00%
发文量
69
审稿时长
6 months
期刊介绍: Particle and Fibre Toxicology is an online journal that is open access and peer-reviewed. It covers a range of disciplines such as material science, biomaterials, and nanomedicine, focusing on the toxicological effects of particles and fibres. The journal serves as a platform for scientific debate and communication among toxicologists and scientists from different fields who work with particle and fibre materials. The main objective of the journal is to deepen our understanding of the physico-chemical properties of particles, their potential for human exposure, and the resulting biological effects. It also addresses regulatory issues related to particle exposure in workplaces and the general environment. Moreover, the journal recognizes that there are various situations where particles can pose a toxicological threat, such as the use of old materials in new applications or the introduction of new materials altogether. By encompassing all these disciplines, Particle and Fibre Toxicology provides a comprehensive source for research in this field.
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