Morgan Daniel L, Flake Gordon P, Kirby Patrick J, Palmer Scott M
Respiratory Toxicology, Laboratory of Molecular Toxicology, National Toxicology Program/National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
Toxicol Sci. 2008 May;103(1):169-80. doi: 10.1093/toxsci/kfn016. Epub 2008 Jan 27.
Diacetyl, a component of artificial butter flavoring, is a potential etiological agent of obliterative bronchiolitis (OB); however, the toxic dose and mechanisms of toxicity remain controversial. We evaluated the respiratory toxicity of diacetyl in a murine model using several exposure profiles relevant to workplace conditions at microwave popcorn packaging plants. Male C57Bl/6 mice were exposed to inhaled diacetyl across several concentrations and duration profiles, or by direct oropharyngeal aspiration. Effects of diacetyl on the respiratory tract were evaluated by histopathology and BALF analyses. Subacute exposure to 200 or 400 ppm diacetyl for 5 days caused deaths, necrotizing rhinitis, necrotizing laryngitis and bronchitis. Reducing the exposure to 1 h/day (100, 200, 400 ppm) for 4 weeks resulted in less nasal and laryngeal toxicity, but led to peribronchial and peribronchiolar lymphocytic inflammation. A similar pattern was observed with intermittent high-dose exposures at 1200 ppm (15 min, twice a day, 4 weeks). Subchronic exposures to 100 ppm (6 h/day, 12 weeks) caused moderate nasal injury, and peribronchial lymphocytic inflammation accompanied by epithelial atrophy, denudation, and regeneration. Treatment with 400 mg/kg by oropharyngeal aspiration to bypass the nose caused foci of fibrohistiocytic proliferation with little or no inflammation at the junction of the terminal bronchiole and alveolar duct. Depending on the route and duration of exposure, diacetyl causes significant epithelial injury, peribronchial lymphocytic inflammation, or fibrohistiocytic lesions in the terminal bronchioles. Collectively these results indicate that clinically relevant diacetyl exposures result in a pattern of injury that replicates features of human OB.
双乙酰是人造黄油香料的一种成分,是闭塞性细支气管炎(OB)的潜在病因;然而,其毒性剂量和毒性机制仍存在争议。我们在小鼠模型中使用与微波爆米花包装厂工作场所条件相关的几种暴露情况评估了双乙酰的呼吸道毒性。雄性C57Bl/6小鼠通过几种浓度和持续时间的暴露情况吸入双乙酰,或通过直接经口咽吸入。通过组织病理学和支气管肺泡灌洗(BALF)分析评估双乙酰对呼吸道的影响。亚急性暴露于200或400 ppm双乙酰5天导致死亡、坏死性鼻炎、坏死性喉炎和支气管炎。将暴露时间减少到每天1小时(100、200、400 ppm),持续4周,导致鼻腔和喉部毒性减轻,但导致支气管周围和细支气管周围淋巴细胞炎症。在1200 ppm(15分钟,每天两次,4周)的间歇性高剂量暴露中也观察到类似模式。亚慢性暴露于100 ppm(每天6小时,12周)导致中度鼻腔损伤,以及支气管周围淋巴细胞炎症,并伴有上皮萎缩、剥脱和再生。通过经口咽吸入400 mg/kg以绕过鼻腔进行治疗,在终末细支气管和肺泡管交界处引起纤维组织细胞增生灶,炎症很少或没有。根据暴露途径和持续时间,双乙酰会导致终末细支气管出现明显的上皮损伤、支气管周围淋巴细胞炎症或纤维组织细胞病变。总体而言,这些结果表明,与临床相关的双乙酰暴露会导致一种损伤模式,重现人类OB的特征。