Stebbins K E, Quast J F, Haut K T, Stott W T
Toxicology & Environmental Research and Consulting, The Dow Chemical Company, 1803 Building, Midland, Michigan 48674, USA.
Regul Toxicol Pharmacol. 1999 Dec;30(3):233-43. doi: 10.1006/rtph.1999.1352.
The potential toxicologic effects to dogs of 1,3-dichloropropene (1, 3-D), a soil fumigant used for the control of nematodes, were investigated. The 13-week subchronic toxicity study consisted of male and female beagle dogs (4/sex/dose group) given approximately 0, 5, 15, or 41 mg 1,3-D/kg body wt/day (approximately equivalent amounts of cis and trans isomers) via their diets. The 1-year chronic toxicity study consisted of male and female beagle dogs (4/sex/dose group) provided diets delivering approximately 0, 0.5, 2. 5, or 15 mg/kg body wt/day. The test material was stabilized in the feed by microencapsulation in a starch/sucrose matrix (80/20). In both the 13-week and the 1-year studies, the primary effect of 1,3-D in male and female dogs ingesting a dosage of >/=15 mg/kg/day was hypochromic, microcytic anemia. The anemia was regenerative, with increased erythropoietic activity characterized by polychromasia of erythrocytes and increased numbers of reticulocytes in peripheral blood. In the 13-week study, the anemia in dogs given 41 mg/kg/day progressively worsened over time, while the anemia in dogs given 15 mg/kg/day remained relatively constant between 42 and 90 days of dosing. Partial reversal of the anemia of high-dose animals occurred during a 5-week recovery period following the 13-week dosing regimen. In the 13-week study, terminal fasted body weights of males given 15 or 41 mg/kg/day were decreased 3 and 28%, respectively, and body weights of females given 5, 15, or 41 mg/kg/day were decreased 4.5, 12, and 24%, respectively, relative to controls. Males given 5 mg/kg/day for 13 weeks had no change in body weights relative to controls. In the 1-year study, the hypochromic microcytic anemia in dogs given 15 mg/kg/day remained relatively constant in severity between 3 and 12 months of treatment. Histopathologic alterations associated with anemia in the 1-year study consisted of increased hematopoiesis of the bone marrow and increased extramedullary hematopoiesis of the spleen. Body weights of males given 15 mg/kg/day were 5-12% lower than controls during the first 13 weeks of the study and 13-19% lower than controls during the remaining 9 months. Body weights of females given 15 mg/kg/day were 5-14% lower than controls over the majority of the dosing period. Males and females given 0.5 or 2.5 mg/kg/day for 1 year had no change in body weights relative to controls. A no-observed-effect level of 2.5 mg/kg/day was established for male and female dogs from the 1-year study.
对用于防治线虫的土壤熏蒸剂1,3 - 二氯丙烯(1,3 - D)对犬类的潜在毒理学影响进行了研究。为期13周的亚慢性毒性研究中,将雄性和雌性比格犬(每组性别各4只)通过饮食给予约0、5、15或41毫克1,3 - D/千克体重/天(顺式和反式异构体的量大致相等)。为期1年的慢性毒性研究中,雄性和雌性比格犬(每组性别各4只)的饮食中提供约0、0.5、2.5或15毫克/千克体重/天。测试材料通过在淀粉/蔗糖基质(80/20)中进行微囊化而在饲料中稳定化。在13周和1年的研究中,摄入剂量≥15毫克/千克/天的雄性和雌性犬中,1,3 - D的主要影响是低色素性、小细胞性贫血。这种贫血是再生性的,其特征是红细胞生成活性增加,表现为红细胞的多染性和外周血中网织红细胞数量增加。在13周的研究中,给予41毫克/千克/天的犬的贫血随时间逐渐恶化,而给予15毫克/千克/天的犬的贫血在给药42至90天之间保持相对稳定。在13周给药方案后的5周恢复期内,高剂量动物的贫血部分得到逆转。在13周的研究中,给予15或41毫克/千克/天的雄性犬的终末禁食体重分别下降了3%和28%,给予5、15或41毫克/千克/天的雌性犬的体重分别下降了4.5%、12%和24%,相对于对照组。给予5毫克/千克/天达13周的雄性犬体重相对于对照组没有变化。在1年的研究中,给予15毫克/千克/天的犬的低色素性小细胞性贫血在治疗3至12个月期间严重程度保持相对稳定。1年研究中与贫血相关的组织病理学改变包括骨髓造血增加和脾脏髓外造血增加。在研究的前13周,给予15毫克/千克/天的雄性犬体重比对照组低5 - 12%,在其余9个月中比对照组低13 - 19%。在给药期的大部分时间里,给予15毫克/千克/天的雌性犬体重比对照组低5 - 14%。给予0.5或2.5毫克/千克/天达1年的雄性和雌性犬体重相对于对照组没有变化。根据1年的研究确定雄性和雌性犬的无观察到有害作用水平为2.5毫克/千克/天。