Angerhofer Richard A, Michie Mark W, Leach Glenn J, Johnson Mark S, Reddy Gunda
US Army Public Health Command, Army Institute of Public Health, Toxicology Portfolio Aberdeen Proving Ground, Aberdeen, MD, USA.
US Army Public Health Command, Army Institute of Public Health, Toxicology Portfolio Aberdeen Proving Ground, Aberdeen, MD, USA
Int J Toxicol. 2014 Sep-Oct;33(5):393-402. doi: 10.1177/1091581814547541. Epub 2014 Aug 27.
Thiodiglycol (TDG) is the main product of sulfur mustard hydrolysis and is an environmental contaminant. Subacute and subchronic oral toxicity studies with TDG were conducted in Sprague-Dawley rats. Neat TDG was administered by gavage at doses of 157, 313, 625, 1250, 2500, 5000, and 9999 mg/kg/d, 5 days per week, for 14 days. In the 14-day study, decreased body weight and food consumption were observed at 5000 mg/kg/d. In the 90-day study, rats received neat TDG at doses of 50, 500, or 5000 mg/kg/d for 5 days per week. A fourth group served as a sham control. Individual body weight and food consumption were measured weekly. At termination of the experiment, urine, blood, and tissue samples were collected. Rats displayed significant decreased body weight with no effect on food consumption following administration of TDG at 5000 mg/kg/d. Both male and female rats showed significant increased kidney weights at 5000 mg/kg/d. The organ to body weight ratios increased significantly for liver, kidneys, testes, and brain in males and adrenals in females for 5000 mg/kg/d. At all doses of TDG, hematological and clinical parameters and tissue histopathology remained unaltered. The no observed adverse effect level (NOAEL) for oral subchronic toxicity was 500 mg/kg/d. Benchmark dose (BMD) was derived from the decreased gain in body weight that was seen in male rats. A BMD based on a 10% decrease in body weight was 1704 mg/kg/d, and the lower confidence limit on the dose BMD, the BMDL, was 372 mg/kg/d.
硫代二甘醇(TDG)是芥子气水解的主要产物,也是一种环境污染物。在斯普拉格-道利大鼠中进行了TDG的亚急性和亚慢性经口毒性研究。将纯TDG以157、313、625、1250、2500、5000和9999 mg/kg/d的剂量通过灌胃给药,每周给药5天,持续14天。在为期14天的研究中,在5000 mg/kg/d剂量下观察到体重和食物摄入量下降。在为期90天的研究中,大鼠以50、500或5000 mg/kg/d的剂量接受纯TDG,每周给药5天。第四组作为假手术对照组。每周测量个体体重和食物摄入量。在实验结束时,收集尿液、血液和组织样本。在给予5000 mg/kg/d的TDG后,大鼠体重显著下降,但对食物摄入量没有影响。在5000 mg/kg/d剂量下,雄性和雌性大鼠的肾脏重量均显著增加。在5000 mg/kg/d剂量下,雄性大鼠的肝脏、肾脏、睾丸和大脑以及雌性大鼠的肾上腺的器官与体重比显著增加。在所有TDG剂量下,血液学和临床参数以及组织组织病理学均未改变。经口亚慢性毒性的未观察到不良反应水平(NOAEL)为500 mg/kg/d。基准剂量(BMD)源自雄性大鼠体重增加的减少。基于体重下降10%的BMD为1704 mg/kg/d,剂量BMD的下限置信限(BMDL)为372 mg/kg/d。