兔囊虫病复方制剂慢性毒性参数的测定

М. В. Богач, вет, професор Л. В наук, Пероцька, доцент Д. М. Богач канд. вет. наук, О філософіїО., Горобей
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引用次数: 0

摘要

本文介绍了一种经小白鼠胃内给药治疗兔囊虫病的方法的临床前试验数据。猪状带绦虫是一种寄生在狗和其他食肉动物小肠上的绦虫,它是一种通过食物或水摄入带绦虫卵而引起的疾病。由于入侵,身体失去了充分发挥功能的能力,免疫系统对传染病的抵抗力下降。为了避免疾病的传播,有必要及时做出诊断。所获得的数据可用于采取必要的防治虫害措施,并对防止选择性使用抗寄生虫剂可能导致驱虫抗药性具有重要意义。在实验条件下,测定研制的复合抗寄生虫剂治疗兔囊虫病对小白鼠的慢性毒性参数。试验组动物每天给予0.0002 dm3的药物水混合液,其中含有以下剂量的药物,连续12天:1/100 DL50 - 16.80 mg/kg (I组);1/50 DL50 - 33.58 mg/kg (II组);1/25 DL50 - 67.18 mg/kg (III组)。末次给药后第二天,小鼠在轻度乙醚麻醉条件下,取血样进行形态学和生化研究。1/50 DL50和1/25 DL50剂量的兔囊虫治疗剂与对照组相比,血红蛋白含量和红细胞计数略有下降,但对实验动物的骨髓红细胞生成没有抑制作用。淋巴细胞数量的减少和中性粒细胞水平的轻微增加被记录下来,这表明增加剂量的药物活性物质的刺激作用。根据化学物质的危险程度分类(DST 12.1.007-76),它属于“中毒性物质”一类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DETERMINATION OF THE CHRONIC TOXICITY PARAMETERS OF THE COMPLEX REMEDY FOR THE TREATMENT OF CYSTICERCOSIS IN RABBITS
The article presents the data of a preclinical test of a means for the treatment of cysticercosis in rabbits by intra-gastric administration to white mice. Cysticercus pisiformis is a disease caused by ingestion of eggs of Taenia pisiformis in food or water, a tapeworm that parasitizes the small intestine of dogs and other carnivores. As a result of the invasion, the body loses its ability to fully function, the resistance of the immune system to infectious diseases decreases. In order to avoid the spread of the disease, it is necessary to make a timely diagnosis. The obtained data can be used to take the necessary measures against infestations and are important to prevent the selective use of anti-parasitic agents, which can lead to anthelmintic resistance. The purpose of the work was to determine the parameters of chronic toxicity of the developed complex anti-parasitic agent for the treatment of rabbits for cysticercosis on white mice under experimental conditions. The animals of the experimental groups were given an aqueous mixture of 0.0002 dm3 of the drug containing the following doses of the drug daily for 12 days: 1/100 DL50 ‒ 16.80 mg/kg (I group); 1/50 DL50 ‒ 33.58 mg/kg (II group); 1/25 DL50 ‒ 67.18 mg/kg (III group). On the next day after the last administration of the drug, on mice, under the condition of light ether narcosis, blood samples were taken for morphological and biochemical studies. The agent for the treatment of cysticercosis in rabbits, at doses of 1/50 DL50 and 1/25 DL50, resulted in a slight decrease in hemoglobin content and erythrocyte count compared to the control, but it did not suppress bone marrow erythropoiesis in laboratory animals. A decrease in the number of lymphocytes and a slight increase in the level of neutrophils were recorded, which indicates the irritating effect of increased doses of the active substance of the drug. According to the classification of chemical substances by degree of danger (DST 12.1.007–76), it belongs to the class of "moderately toxic substances".
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