“Protostop”治疗犊牛隐孢子虫病的安全性研究

N. Gavrilova, L. Belova, Y. A. Shcherbina
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摘要

将含有100.0 mg硫酸帕罗霉素1.0 g的Protostop药物用于隐孢子虫病犊牛。实验组动物分别以每1 kg动物体重250和350 mg的剂量口服,疗程分别为3天和5天。在使用前,将单剂量的药物通过在粉末中加入液体溶解在水中。对照组小牛接受对症治疗,旨在消除腹泻综合征。在疗程开始前和疗程结束后第10天,分别取实验组和对照组动物的血进行一般临床分析。记录给药前和给药后第4、6、8、12、15天动物的生理状态。研究发现,用250 mg/kg和350 mg/kg的Protostop药物治疗隐孢子虫病犊牛,在3天和5天的疗程中没有引起动物身体的负面变化。治疗开始前,各组犊牛血红蛋白含量均低于参考值。血小板减少症、嗜酸性粒细胞增多症和嗜中性粒细胞增多症也有记录,并注意到ESR升高。用药后,嗜酸性粒细胞、节段性中性粒细胞、ESR等指标均在参考值范围内,血红蛋白水平略有升高。用药后,嗜酸性粒细胞、节段性中性粒细胞、ESR指标均在参考值范围内,血红蛋白水平略有升高。在对照组中,尽管对症治疗,但观察到嗜酸性粒细胞增多,节段性中性粒细胞和ESR百分比增加。在整个治疗过程中,以及治疗结束后的10天内,犊牛的生理状态没有出现恶化、粘膜充血、瘙痒或其他可能出现药物副作用的迹象。
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Study of the safety of application of the drug "Protostop" in cryptosporidiosis of calves
The drug "Protostop" containing 100.0 mg of paromomycin sulfate in 1.0 g was used in calves with cryptosporidiosis.The animals in the experimental groups were given the drug at a dose of 250 and 350 mg per 1 kg of animal weight individually, orally, in courses of 3 and 5 days, respectively. Before use, a single dose of the drug was dissolved in water by adding liquid to the powder. The calves of the control group received symptomatic treatment aimed at eliminating the diarrheal syndrome. Before the start of the therapeutic course and on the 10th day after its completion, blood was taken from the animals of the experimental and control groups for general clinical analysis.The physiological state of the animals was recorded before the administration of the drug and on the 4th, 6th, 8th, 12th and 15th day from the start of treatment. It was found that the treatment of calves with cryptosporidiosis with the drug "Protostop" at a dose of 250 mg/kg and 350 mg/kg in 3 and 5 -day courses did not cause negative changes in the animals' bodies. Before the start of the treatment, the hemoglobin content of the calves in all groups were lower than the reference values. Thrombocytopenia, eosinophilia and neutrophilia were also recorded and an increase in ESR was noted. After using the drug, the indices of eosinophils, segmented neutrophils and ESR were within the reference values, the hemoglobin level slightly increased. After using the drug, the indicators for eosinophils, segmented neutrophils and ESR were within the reference values, while the hemoglobin levels were slightly increased. Calves in the control group, despite symptomatic treatment, eosinophilia were observed with an increase in the percentage of segmented neutrophils and ESR. During the course of treatment, as well as 10 days after its completion, the calves showed no deterioration in their physiological state, hyperemia of the mucous membranes, itching or other signs indicating a possible side effect to the drug.
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