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首页> 外文期刊>Preventive Veterinary Medicine >Comparison of therapeutic efficacy of different drugs against Trypanosoma vivax on experimentally infected cattle
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Comparison of therapeutic efficacy of different drugs against Trypanosoma vivax on experimentally infected cattle

机译:不同药物对实验感染牛锥虫瘤的治疗疗效的比较

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In this study, we evaluated the therapeutic efficacy of diminazene diaceturate at a dose of 7 mg/kg (DA), imidocarb dipropionate at 4.8 mg/kg (IMD), isometamidium chloride at 0.5 and 1.0 mg/kg (ISM 0.5 and ISM 1.0) and combinations applied through different methods to treat Trypanosoma vivax in experimentally infected calves. Thirty male Girolando calves were kept indoors and infected intravenously with T. vivax trypomastigotes (approximately 1 x 106). On D-1, the calves were randomized based on the quantity of infecting parasites per animal, yielding six groups of five animals each: G1: positive control group without treatment; G2 animals treated with DA on Day 0 intramuscularly (IM); G3 animals treated with IMD on Day 0 and D + 14 sub-cutaneously; G4 animals treated with ISM 0.5 on Day 0 IM; G5 animals treated with ISM 1.0 on Day 0 IM; G6 animals received DA on Day 0 and ISM 1.0 on D + 14, both IM. Throughout 180 days, blood samples were collected for the evaluation of T. vivax using the Woo, Brener and PCR methods. The results indicated that the treatment protocols with DA and/or ISM 0.5 and ISM 1.0 had high efficacy (100 %) against T. vivax. Interestingly, cattle that received ISM remained free of parasites until D + 180. In contrast, animals treated with IMD had relapsed T. vivax detected on the 10th and 14th days post-treatment (DPT). Cattle that received ISM 1.0 did not exhibit relapsed T. vivax in the blood, even after reinfection performed on the 50th DPT. However, treatment with DA on Day 0 failed to prevent a new infection of T. vivax on the 50th DPT. The animals that received ISM 1.0 had a transient decrease in packed cell volume similar to that found in the control group. The reappearance of T. vivax in herds in Brazil treated with DA likely occurred due to the short half-life of the drug and not necessarily due to T. vivax resistance to DA.
机译:在该研究中,我们评估了在4.8mg / kg(IMD)的7mg / kg(da),咪啶二丙酸酯,氯化物的剂量为0.5和1.0mg / kg(ISM 0.5和ISM 1.0 )通过不同方法应用的组合治疗在实验感染的小牛中的锥虫瘤vivax。三十只雄性吉拉莫尔犊牛在室内进行,静脉内感染vivax胰蛋白酶(约1 x 106)。在D-1上,基于每只动物的感染寄生虫的量随机分组,产生六组五只动物:G1:阳性对照组无需治疗;在第0天肌肉内用DA治疗G2动物(IM); G3动物在第0天和D + 14日使用IMD治疗; G4动物用ISM 0.5在第0天施用IM;在第0天含有ISM 1.0的G5动物; G6动物在D + 14时第0天和ISM 1.0接受DA。在整个180天内,收集血液样品用于使用Woo,Brener和PCR方法评估T.Vivax。结果表明,具有DA和/或ISM 0.5和ISM 1.0的治疗方案对T.Vivax具有高疗效(100%)。有趣的是,接受ISM的牛仍然没有寄生虫,直到D + 180左右。相反,用IMD处理的动物在治疗后第10天和第14天检测到vivax(DPT)。接受ISM 1.0的牛在血液中没有表现出在血液中复发,即使在第50次DPT上进行了重新感染后,也是如此。然而,第0天的DA治疗未能在第50次DPT上预防vivax的新感染。接受ISM 1.0的动物具有与对照组中的填充细胞体积的瞬时减少相似。由于药物的半衰期短而且由于T.Vivax抗性的耐受性而导致的牛群中,在巴西治疗的巴西群中的T.Vivax的重新分析。

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