观察小鼠腹腔内给予多壁碳纳米管引起炎症的时间过程。

Masanori Horie, Sakiko Sugino, Tomoki Ohno
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引用次数: 0

摘要

目的:了解多壁碳纳米管(MWCNT)引起的炎症随时间的进展。方法:C57BL/6N小鼠腹腔内分别给予低剂量和高剂量(分别为0.05和1.0mg/只)的两种MWCNT。根据细胞因子水平和病理学观察对炎症进行评估,直至给药后6个月。在给药后1周、1个月、3个月和6个月收集腹腔灌洗液并进行分析。在给予高剂量MWCNT-7后3个月,IL-6的表达显著增加。结果:在给予MWCNT之一MWCNT-7的组中观察到显著的炎症。另一方面,另一个MWCNT处理组的炎症比MWCNT-7处理组的轻。MWCNT-7在实验期间诱导了明显的炎症,但没有诱导肿瘤形成。炎症反应是MWCNT最重要的生物反应之一。结论:暴露后三个月成为腹膜内给药MWCNT-7有害影响的转折点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Follow the time course of inflammation caused by intraperitoneal administration of multi-wall carbon nanotubes in mice.

Objective: Understand the progress of inflammation over time caused by multi-walled carbon nanotubes (MWCNT).

Methods: Two types of MWCNTs were administered to C57BL/6N mice via intraperitoneal administration at low and high doses (0.05 and 1.0 mg/mouse, respectively). Inflammation was evaluated until 6 months after administration based on cytokine levels and pathological observations. The abdominal cavity lavage fluid was collected and analyzed 1 week, 1, 3, and 6 month(s) after administration. IL-6 expression markedly increased 3 months after the administration of high-dose MWCNT-7.

Results: Notable inflammation was observed in the groups administered with one of the MWCNT, MWCNT-7. On the other hand, inflammation in another MWCNT-treated group was milder than that in the MWCNT-7-treated group. MWCNT-7 induced pronounced inflammation but did not induce tumor formation during the experimental period. Inflammation reaction is one of the most important biological responses to MWCNT.

Conclusion: Three months post-exposure becomes a turning point for the harmful effects of the intraperitoneally administered MWCNT-7.

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来源期刊
International Journal of Immunopathology and Pharmacology
International Journal of Immunopathology and Pharmacology Immunology and Microbiology-Immunology
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发文量
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期刊介绍: International Journal of Immunopathology and Pharmacology is an Open Access peer-reviewed journal publishing original papers describing research in the fields of immunology, pathology and pharmacology. The intention is that the journal should reflect both the experimental and clinical aspects of immunology as well as advances in the understanding of the pathology and pharmacology of the immune system.
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