Patuxent Wildlife Research Center, U.S. Geological Survey, Department of the Interior, 10300 Baltimore Avenue, BARC East-308, Beltsville, MD 20705, USA.
Ecotoxicol Environ Saf. 2010 Sep;73(6):1159-64. doi: 10.1016/j.ecoenv.2010.05.021. Epub 2010 Jun 30.
The anticoagulant rodenticide diphacinone was slightly toxic (acute oral LD50 2014 mg/kg) to Northern bobwhite (Colinus virginianus) in a 14-day acute toxicity trial. Precise and sensitive assays of blood clotting (prothrombin time, Russell's Viper venom time, and thrombin clotting time) were adapted for use in quail, and this combination of assays is recommended to measure the effects of anticoagulant rodenticides. A single oral sublethal dose of diphacinone (434 mg/kg body weight) prolonged clotting time at 48 h post-dose compared to controls. At 783 mg/kg (approximate LD02), clotting time was prolonged at both 24 and 48 h post-dose. Prolongation of in vitro clotting time reflects impaired coagulation complex activity, and was detected before overt signs of toxicity were apparent at the greatest dosages (2868 and 3666 mg/kg) in the acute toxicity trial. These clotting time assays and toxicity data will assist in the development of a pharmacodynamic model to predict toxicity, and also facilitate rodenticide hazard and risk assessments in avian species.
在为期 14 天的急性毒性试验中,抗凝血杀鼠剂二苯并呋喃对北美野鹌鹑(Colinus virginianus)具有轻微毒性(急性经口 LD50 为 2014mg/kg)。凝血(凝血酶原时间、罗素蝰蛇毒液时间和凝血酶凝固时间)的精确和敏感测定法已适用于鹌鹑,并建议将这些测定法组合用于测量抗凝血杀鼠剂的效果。单次口服亚致死剂量的二苯并呋喃(434mg/kg 体重)与对照组相比,在给药后 48 小时延长了凝血时间。在 783mg/kg(近似 LD02)时,在给药后 24 和 48 小时,凝血时间均延长。体外凝血时间的延长反映了凝血复合物活性受损,并且在急性毒性试验中最大剂量(2868 和 3666mg/kg)出现明显毒性迹象之前就已检测到。这些凝血时间测定和毒性数据将有助于开发一种药效动力学模型来预测毒性,同时也有助于评估鸟类物种中杀鼠剂的危害和风险。