Kaewamatawong Theerayuth, Shimada Akinori, Okajima Mina, Inoue Hiromi, Morita Takehito, Inoue Kenichiro, Takano Hirohisa
Department of Veterinary Pathology, Tottori University, Minami 4-101, Koyama, Tottori-shi, Tottori, Japan.
Toxicol Pathol. 2006;34(7):958-65. doi: 10.1080/01926230601094552.
To study the acute and subacute lung toxicity of low dose of ultrafine colloidal silica particles (UFCSs), mice were intratracheally instilled with 0, 0.3, 3, 10, 30 or 100 microg of UFCSs. Cellular and biochemical parameters in bronchoalveolar lavage fluid (BALF), histological alteration and the body weight were determined at 3 days after instillation. Exposure to 30 or 100 microg of UFCSs produced moderate to severe pulmonary inflammation and tissue injury. To investigate the time response, mice were instilled with 30 microg of UFCSs and sacrificed at intervals from 1 to 30 days post-exposure. UFCSs induced moderate pulmonary inflammation and injury on BALF indices at acute period; however, these changes gradually regressed until recovery during the experiment. Concomitant histopathological and laminin immunohistochemical findings generally correlated to BALF data. TUNEL analyses in UFCSs-treated animals showed a significant increase of the apoptotic index in lung parenchyma at all observation times. 8-OHdG expression occurred in lung epithelial cells and activated macrophages, which correlated to lung lesions in UFCSs-treated mice. These findings suggest that instillation of a small dose of UFCSs causes transient acute moderate lung inflammation and tissue damage. Oxidative stress and apoptosis may underlie the lung tissue injury induction.
为研究低剂量超细胶体二氧化硅颗粒(UFCSs)的急性和亚急性肺毒性,给小鼠经气管内滴注0、0.3、3、10、30或100微克的UFCSs。在滴注后3天测定支气管肺泡灌洗液(BALF)中的细胞和生化参数、组织学改变及体重。暴露于30或100微克的UFCSs会产生中度至重度的肺部炎症和组织损伤。为研究时间反应,给小鼠滴注30微克的UFCSs,并在暴露后1至30天的不同时间点处死。UFCSs在急性期可诱导BALF指标出现中度肺部炎症和损伤;然而,在实验过程中这些变化逐渐消退直至恢复。同时,组织病理学和层粘连蛋白免疫组化结果通常与BALF数据相关。对UFCSs处理动物的TUNEL分析显示,在所有观察时间点肺实质中的凋亡指数均显著增加。8-OHdG表达出现在肺上皮细胞和活化的巨噬细胞中,这与UFCSs处理小鼠的肺部病变相关。这些发现表明,滴注小剂量的UFCSs会导致短暂的急性中度肺部炎症和组织损伤。氧化应激和细胞凋亡可能是诱导肺组织损伤的原因。