Wu Y Z, Kan B T, Wang W J, Zhang Z C, Jia J E, Li X Q, Han J, Yu L J, Jian X D
Shandong university school of public health, Jinan 250014, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2018 Nov 20;36(11):813-818. doi: 10.3760/cma.j.issn.1001-9391.2018.11.004.
To explore the acute toxicity of Diquat in mice and to calculate the median lethal dose (LD(50)) of Diquat to rats and observe the pathological changes of tissues and organs in rats with different concentrations of Diquat. Diquat solution of 50 mg/kg was prepared freshly with 1 000 mg of Diquat and dilute the solution with water to a total of 20 ml. A total of 99 healthy adult male Wistar rats were randomly divided into part one, part two and control groups. In the first part, 36 rats were randomly divided into 4 groups: 100 mg/kg group, 200 mg/kg group, 300 mg/kg group and 400 mg/kg group, which were treated with 100 mg/kg, 200 mg/kg, 300 mg/kg and 400 mg/kg of Diquat solution by gavage, respectively. The death and symptoms of poisoning after intragastric administration were recorded, and the maximum tolerated dose and absolute lethal dose were measured. In the second part, 54 rats were randomly divided into 6 groups: 200 mg/kg group, 220 mg/kg group, 240 mg/kg group, 260 mg/kg、280 mg/kg group and 300 mg/kg group, whichwere treated with 200 mg/kg, 220 mg/kg, 240 mg/kg, 260 mg/kg, 280 mg/kg and 300 mg/kg of Diquat solution by gavage, respectively. The survival of rats in different concentration of Diquat was observed and the LD(50) was calculated by Excel processing the formula of Koch's method. The control group were given equal volume water under the same experimental conditions. And moreover, the lungs, kidneys, hearts, livers, and brain tissues were collected and fixed by formaldehyde, embedded by paraffin, and sectioned for histopathological light microscopy. The maximum tolerated dose was 240 mg/kg and the absolute lethal dose was 300 mg/kg. The LD(50) of Diquat for Rats was 280.58 mg/kg. The high-dose group had significantly more organ damage than the lowdose group after diquat poisoning. The determination of the half-lethal dose of diquat, at the same time observed multiple organs damaged in rats after the diquat quickly poisoned. Kidneys, lungs and heart might be the main organ which was heavily damaged. With the extension of observation time, the organ damage of rats exposed to small doses gradually stabilized.
探讨敌草快对小鼠的急性毒性,计算敌草快对大鼠的半数致死量(LD50),并观察不同浓度敌草快染毒大鼠组织器官的病理变化。用1000mg敌草快新鲜配制50mg/kg的敌草快溶液,加水稀释至总体积20ml。将99只健康成年雄性Wistar大鼠随机分为第一部分、第二部分和对照组。第一部分,将36只大鼠随机分为4组:100mg/kg组、200mg/kg组、300mg/kg组和400mg/kg组,分别经口灌胃给予100mg/kg、200mg/kg、300mg/kg和400mg/kg的敌草快溶液。记录灌胃给药后的死亡及中毒症状,测定最大耐受量和绝对致死量。第二部分,将54只大鼠随机分为6组:200mg/kg组、220mg/kg组、240mg/kg组、260mg/kg组、280mg/kg组和300mg/kg组,分别经口灌胃给予200mg/kg、220mg/kg、240mg/kg、260mg/kg、280mg/kg和300mg/kg的敌草快溶液。观察不同浓度敌草快染毒大鼠的存活情况,用Excel处理寇氏法公式计算LD50。对照组在相同实验条件下给予等体积的水。此外,采集肺、肾、心、肝和脑组织,用甲醛固定,石蜡包埋,切片进行组织病理学光学显微镜检查。最大耐受量为240mg/kg,绝对致死量为300mg/kg。敌草快对大鼠的LD50为280.58mg/kg。敌草快中毒后,高剂量组的器官损伤明显多于低剂量组。测定敌草快的半数致死量,同时观察敌草快快速染毒后大鼠多个器官的损伤情况。肾、肺和心脏可能是损伤较重的心要器官。随着观察时间的延长,小剂量染毒大鼠的器官损伤逐渐稳定。