Sarangapani Ramesh, Teeguarden Justin G, Gentry P Robinan, Clewell Harvey J, Barton Hugh A, Bogdanffy Matthew S
ICF Consulting, Research Triangle Park, North Carolina, USA.
Inhal Toxicol. 2004 Aug;16(9):593-605. doi: 10.1080/08958370490464562.
Dimethyl sulfate (DMS) is a volatile sulfuric acid ester used principally as a methylating agent in a wide variety of industrial applications. DMS reacts with organic macromolecules by a SN2 mechanism. The weight of experimental evidence suggests that DMS possesses genotoxic and carcinogenic potential. Inhalation studies have shown that repeated exposure to DMS leads to tumors in the nasal cavity and lower respiratory tract in both rats and mice. Here we present a quantitative assessment for cross-species dose extrapolation for inhaled DMS using a physiologically based pharmacokinetic (PBPK) model. The model is designed to simulate N7-methylguanine (N7 mG) DNA adduct levels in the nasal mucosa following DMS exposure in rats and humans. This model was parameterized and predictions were tested by comparison against experimentally measured N7 mG DNA adduct levels in rat nasal mucosa following inhalation exposure to DMS. The model-based interspecies dose comparison, using N7 mG adduct levels in the nasal respiratory tissue as the appropriate dose metrics, predicts a dose rate seven times higher in rats compared to humans.
硫酸二甲酯(DMS)是一种挥发性硫酸酯,主要用作甲基化剂,广泛应用于各种工业领域。DMS 通过 SN2 机制与有机大分子发生反应。大量实验证据表明,DMS 具有遗传毒性和致癌潜力。吸入研究表明,大鼠和小鼠反复接触 DMS 会导致鼻腔和下呼吸道肿瘤。在此,我们使用基于生理的药代动力学(PBPK)模型对吸入 DMS 的跨物种剂量外推进行了定量评估。该模型旨在模拟大鼠和人类接触 DMS 后鼻腔黏膜中 N7-甲基鸟嘌呤(N7 mG)DNA 加合物水平。对该模型进行了参数化,并通过与吸入 DMS 后大鼠鼻腔黏膜中实验测量的 N7 mG DNA 加合物水平进行比较来检验预测结果。基于模型的种间剂量比较,以鼻腔呼吸组织中的 N7 mG 加合物水平作为合适的剂量指标,预测大鼠的剂量率是人类的七倍。