Warheit D B, Carakostas M C, Hartsky M A, Hansen J F
Haskell Laboratory for Toxicology and Industrial Medicine, E. I. du Pont de Nemours and Company, Newark, Delaware 19714.
Toxicol Appl Pharmacol. 1991 Feb;107(2):350-68. doi: 10.1016/0041-008x(91)90215-z.
This paper describes a short-term inhalation bioassay for evaluating the lung toxicity of inhaled particulate materials. To validate the method, rats were exposed for 6 hr or 3 days to various concentrations of either aerosolized alpha-quartz silica or carbonyl iron particles. Cells and fluids from groups of sham- and dust-exposed animals were recovered by bronchoalveolar lavage (BAL). Alkaline phosphatase, lactate dehydrogenase (LDH), and protein values were measured in BAL fluids at several time points postexposure. Cells were identified, counted, and evaluated for viability. Pulmonary macrophages (PM) were cultured and studied for morphology, chemotaxis, and phagocytosis by scanning electron microscopy. The lungs of additional exposed animals were processed for histopathology and transmission electron microscopy. Brief exposures to silica elicited a sustained granulocytic inflammatory response (primarily neutrophils) with concomitant increases in alkaline phosphatase, LDH, and protein in the lavage fluids (p less than 0.05). In addition, PM functional capacity was depressed (p less than 0.05) and histopathologic lesions were observed within 1 month after exposure. In contrast, 6-hr or 3-day exposures to CI produced no cellular, cytotoxic, or alveolar/capillary membrane permeability changes at any time postexposure. PM function was either enhanced or unchanged from controls. These data demonstrate that short-term, high-dose inhalation exposures of silica produce effects similar to those previously observed using intratracheal instillation or chronic inhalation models, and lend support to this method as a reliable short-term bioassay for evaluating the pulmonary toxicity and mechanisms associated with exposures to new and untested materials.
本文描述了一种用于评估吸入颗粒物肺部毒性的短期吸入生物测定法。为验证该方法,将大鼠暴露于不同浓度的雾化α-石英二氧化硅或羰基铁颗粒中6小时或3天。通过支气管肺泡灌洗(BAL)回收假暴露和粉尘暴露动物组的细胞和液体。在暴露后的几个时间点测量BAL液中的碱性磷酸酶、乳酸脱氢酶(LDH)和蛋白质值。对细胞进行鉴定、计数并评估其活力。培养肺巨噬细胞(PM),并通过扫描电子显微镜研究其形态、趋化性和吞噬作用。对另外一些暴露动物的肺进行组织病理学和透射电子显微镜检查。短期暴露于二氧化硅会引发持续的粒细胞炎症反应(主要是中性粒细胞),同时灌洗液中的碱性磷酸酶、LDH和蛋白质增加(p<0.05)。此外,暴露后1个月内观察到PM功能能力下降(p<0.05)和组织病理学损伤。相比之下,暴露于CI 6小时或3天在暴露后的任何时间都未产生细胞、细胞毒性或肺泡/毛细血管膜通透性变化。PM功能与对照组相比要么增强要么不变。这些数据表明,短期、高剂量吸入二氧化硅产生的效应与先前使用气管内注入或慢性吸入模型观察到的效应相似,并支持该方法作为一种可靠的短期生物测定法,用于评估与新的和未经测试的材料暴露相关的肺部毒性和机制。