Honda Kazumasa, Naya Masato, Takehara Hiroshi, Kataura Hiromichi, Fujita Katsuhide, Ema Makoto
a Research Institute of Science for Safety and Sustainability , National Institute of Advanced Industrial Science and Technology (AIST) , Tsukuba , Japan.
b Technology Research Association for Single Wall Carbon Nanotubes (TASC) , Tsukuba , Japan.
Inhal Toxicol. 2017 Sep;29(11):471-482. doi: 10.1080/08958378.2017.1394930. Epub 2017 Nov 7.
We compared long-term pulmonary toxicities after a single intratracheal instillation of two types of dispersed single-wall carbon nanotubes (SWCNTs), namely, those with relatively long or short linear shapes with average lengths of 8.6 and 0.55 µm, respectively. Both types of SWCNTs were instilled intratracheally in male F344 rats at 0.2 or 1.0 mg/kg (long SWCNTs) or 1.0 mg/kg (short SWCNTs). Pulmonary responses were characterized at 26, 52 and 104 weeks after a single instillation. Inflammatory changes, test substance deposition, test substance engulfment by macrophages, and alveolar wall fibrosis were observed in the lungs of almost all test rats at 52 and 104 weeks after short nanotube instillation. The incidences of these changes were much lower in the long nanotube-treated groups. In almost all rats of the long nanotube-treated groups, fibrosis and epithelium loss in the terminal bronchiole with test substance deposition were observed. These bronchiolar changes were not observed after administering short nanotubes. Both bronchiolo-alveolar adenoma and carcinoma were found in the negative-control group, the high-dose long-nanotube group, and the short-nanotube group at 104 weeks post-instillation, although the incidences were not statistically different. The genotoxicity of the SWCNTs was also evaluated by performing in vivo comet assays with lung cells obtained 26 weeks post-instillation. No significant changes in the percent tail deoxyribonucleic acid were found in any group. These findings suggested that most long SWCNTs were deposited at the terminal bronchioles and that a considerable amount of short SWCNTs reached the alveolus, resulting in chronic inflammatory responses, but no genotoxicity in the lungs.
我们比较了单次气管内滴注两种分散的单壁碳纳米管(SWCNT)后的长期肺部毒性,这两种碳纳米管分别具有相对较长或较短的线性形状,平均长度分别为8.6和0.55微米。两种类型的SWCNT均以0.2或1.0毫克/千克(长SWCNT)或1.0毫克/千克(短SWCNT)的剂量气管内滴注到雄性F344大鼠体内。在单次滴注后的26、52和104周对肺部反应进行表征。在短纳米管滴注后52和104周,几乎所有受试大鼠的肺部均观察到炎症变化、受试物质沉积、巨噬细胞对受试物质的吞噬以及肺泡壁纤维化。这些变化在长纳米管处理组中的发生率要低得多。在几乎所有长纳米管处理组的大鼠中,观察到终末细支气管出现纤维化和上皮丢失以及受试物质沉积。在给予短纳米管后未观察到这些细支气管变化。在滴注后104周,在阴性对照组、高剂量长纳米管组和短纳米管组中均发现了细支气管肺泡腺瘤和癌,尽管发生率无统计学差异。还通过对滴注后26周获得的肺细胞进行体内彗星试验来评估SWCNT的遗传毒性。在任何组中均未发现尾端脱氧核糖核酸百分比有显著变化。这些发现表明,大多数长SWCNT沉积在终末细支气管,相当数量的短SWCNT到达肺泡,导致慢性炎症反应,但在肺部无遗传毒性。