Canton Candela, Ceballos Laura, Fiel César, Moreno Laura, Domingo Yagüez Pablo, Bernat Gisele, Lanusse Carlos, Alvarez Luis
Laboratorio de Farmacología, Centro de Investigación Veterinaria de Tandil (CIVETAN), UNCPBA-CICPBA-CONICET, Facultad de Ciencias Veterinarias, Campus Universitario, 7000 Tandil, Argentina.
Laboratorio de Farmacología, Centro de Investigación Veterinaria de Tandil (CIVETAN), UNCPBA-CICPBA-CONICET, Facultad de Ciencias Veterinarias, Campus Universitario, 7000 Tandil, Argentina.
Vet Parasitol. 2017 Jan 30;234:40-48. doi: 10.1016/j.vetpar.2016.12.021. Epub 2016 Dec 31.
Nematodicidal combinations have been proposed as a valid strategy to achieve effective nematode control in the presence of drug resistance. The goals of this study were: (1) to compare the clinical efficacy (therapeutic response) of ivermectin (IVM) and ricobendazole (RBZ) given subcutaneously either by separate or combined administration to calves naturally infected with gastrointestinal nematodes resistant to IVM, and (2) to evaluate the potential pharmacokinetic (PK) and/or pharmacodynamic (PD) interactions occurring after the co-administration of both anthelmintics. Sixty male calves naturally infected with gastrointestinal nematodes resistant to IVM were randomly allocated into four groups (n=15). Untreated control: animals not receiving anthelmintic treatment; IVM alone: animals treated with IVM by subcutaneous (SC) injection (0.2mg/kg); RBZ alone: animals received RBZ by the SC route (3.75mg/kg); IVM+RBZ: animals treated with IVM and RBZ (0.2 and 3.75mg/kg, respectively), by SC injection in two separates sites. Eight animals of each treated group were randomly selected to perform the PK study. Plasma samples were taken from those animals up to 28days post-treatment. IVM and RBZ plasma concentrations were quantified by HPLC. The therapeutic response was determined by faecal egg count reduction test (FECRT). The proportions of third-stage larvae (L3) recovered from coprocultures were used to calculate the efficacy against the main parasite genera. The daily total egg deposition for each experimental group was estimated. Similar pharmacokinetic trends were obtained for both IVM and RBZ allying the single-drug and the combined treatments, which indicates the absence of PK interactions between both anthelmintics. The observed overall clinical drug efficacies were 48% (IVM alone), 94% (RBZ alone) and 98% (IVM+RBZ). Haemonchus spp. and Cooperia spp. were recovered in the coproculture after IVM treatment, suggesting that resistance to IVM includes both genera. In fact, the efficacy against Cooperia spp. was 83% (IVM), 98% (RBZ) and 98% (IVM+RBZ), while the efficacy against Haemonchus spp. was 0% (IVM), 97% (RBZ) and 100% (IVM+RBZ). The combination was the only treatment that achieved 100% clinical efficacy against IVM-resistant Haemonchus spp. The total egg excretion was reduced to 49.9% (IVM alone group), 6.3% (RBZ alone group) and 1.8% (IVM+RBZ combined group) compared to the untreated control. Although the combined treatment did not significantly increase the overall clinical efficacy in the current natural field conditions, an additive effect was achieved against IVM-resistant nematodes. In fact, the combination obtained significantly higher efficacy against IVM-resistant Haemonchus spp. than RBZ alone. Additionally, the epidemiological relevance of the reduction in the number of eggs excreted following the combined treatment is not negligible and should be taken into account in future studies. Further work is required to understand the advantages of nematodicidal combinations in different natural anthelmintic resistance scenarios.
杀线虫剂组合已被提议作为在存在耐药性的情况下实现有效控制线虫的一种有效策略。本研究的目的是:(1)比较伊维菌素(IVM)和利苯达唑(RBZ)分别皮下给药或联合给药对自然感染对IVM耐药的胃肠道线虫的犊牛的临床疗效(治疗反应),以及(2)评估两种驱虫药联合给药后可能发生的药代动力学(PK)和/或药效学(PD)相互作用。60头自然感染对IVM耐药的胃肠道线虫的雄性犊牛被随机分为四组(n = 15)。未治疗对照组:未接受驱虫治疗的动物;单独使用IVM组:通过皮下(SC)注射(0.2mg/kg)用IVM治疗的动物;单独使用RBZ组:通过SC途径(3.75mg/kg)接受RBZ的动物;IVM + RBZ组:通过在两个不同部位皮下注射分别用IVM和RBZ(分别为0.2和3.75mg/kg)治疗的动物。每个治疗组随机选择8只动物进行PK研究。在治疗后长达28天从这些动物采集血浆样本。通过高效液相色谱法对IVM和RBZ血浆浓度进行定量。通过粪便虫卵计数减少试验(FECRT)确定治疗反应。从粪便培养物中回收的第三期幼虫(L3)的比例用于计算对主要寄生虫属的疗效。估计每个实验组的每日总虫卵排出量。IVM和RBZ在单药治疗和联合治疗中获得了相似的药代动力学趋势,这表明两种驱虫药之间不存在PK相互作用。观察到的总体临床药物疗效分别为48%(单独使用IVM)、94%(单独使用RBZ)和98%(IVM + RBZ)。IVM治疗后在粪便培养物中回收了血矛线虫属和古柏线虫属,这表明对IVM的耐药性包括这两个属。实际上,对古柏线虫属的疗效分别为83%(IVM)、98%(RBZ)和98%(IVM + RBZ),而对血矛线虫属的疗效分别为0%(IVM)、97%(RBZ)和100%(IVM + RBZ)。联合治疗是唯一对耐IVM的血矛线虫属实现100%临床疗效的治疗方法。与未治疗对照组相比,总虫卵排出量分别降至49.9%(单独使用IVM组)·、6.3%(单独使用RBZ组)和1.8%(IVM + RBZ联合组)。尽管在当前的自然田间条件下联合治疗并未显著提高总体临床疗效,但对耐IVM的线虫实现了相加效应。实际上,联合治疗对耐IVM的血矛线虫属获得的疗效显著高于单独使用RBZ。此外,联合治疗后排出虫卵数量减少的流行病学相关性不可忽视,应在未来研究中予以考虑。需要进一步开展工作以了解杀线虫剂组合在不同自然驱虫抗性情况下的优势。