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不同伊维菌素和多拉菌素制剂对放牧公牛疥螨病防治效果的比较评估

Comparative assessment of different ivermectin and doramectin formulations for mange control in grazing steers.

作者信息

Canton Candela, Muchiut Sebastián, Dominguez María Paula, Lanusse Carlos, Alvarez Luis Ignacio, Lifschitz Adrián

机构信息

Laboratorio de Farmacología, Centro de Investigación Veterinaria de Tandil (CIVETAN), UNCPBA-CICPBA-CONICET, Campus Universitario, Tandil, Buenos Aires, Argentina; Universidad Nacional del Centro de la Provincia de Buenos Aires (UNCPBA), Facultad de Ciencias Veterinarias, Campus Universitario, Tandil, Buenos Aires, Argentina.

Laboratorio de Inmunología y Parasitología, Instituto Nacional de Tecnología Agropecuaria, Estación Experimental Agropecuaria Rafaela, 2300 Rafaela, Santa Fe, Argentina.

出版信息

Vet Parasitol. 2023 Apr;316:109891. doi: 10.1016/j.vetpar.2023.109891. Epub 2023 Feb 4.

DOI:10.1016/j.vetpar.2023.109891
PMID:36780819
Abstract

Psoroptic mange causes relevant losses of productivity in cattle. Macrocyclic lactones are one of the main pharmacological tools recommended for controlling it. The aim of the current work was to compare the relationship between the pharmacokinetic behavior and the effectiveness of both ivermectin (IVM) and doramectin (DRM) following their administration as either the traditional (1 %) or long-acting (3.15-3.5 %) injectable formulations to cattle naturally infected with Psoroptes ovis. The overall work involved three trials (1, 2 and 3) carried out on commercial beef cattle farms (grazing systems). In Trial 1, 20 grazing steers with active mange infection were allocated into 2 groups (n = 10) and treated subcutaneously (SC) with either IVM (1 %) or DRM (1%) at 0.2 mg/kg. In Trial 2, 16 grazing steers with active mange divided in 2 groups (n = 8) were treated SC with either IVM 1 % (0.2 mg/kg) or IVM 3.15 % long-acting (0.63 mg/kg). In Trial 3, 2 groups of mange infected steers (n = 8) were treated SC with either IVM 3.15 % (0.63 mg/kg) or DRM 3.5 % (0.7 mg/kg). Blood samples were collected of each experimental group and the drug systemic availability was estimated by measuring of IVM/DRM concentrations by HPLC. Skin scraping samples were collected from each animal and mites were counted at 14, 21 and 28 days post-treatment. In Trial 1, the mite density score on day 14 was significantly lower for DRM (0.60) compared to IVM (1.80) (P = 0.019). Based on the number of animals clinically cured (negative to the presence of mites), the efficacy of DRM was higher (80 %) than that obtained for IVM (10 %) (P < 0.05). DRM systemic exposure measured as AUC was 1.37-fold higher compared to IVM. In Trial 2, even though IVM exposure was significantly greater after the long-acting (3.15 %) compared to the traditional formulation (1 %), none of the treatments significantly reduced the mite density score, with a percentage of animals cured between 0 % and 37.5 % after both IVM treatments. In Trial 3, the 100 % of cured animals were achieved at day 21 (IVM 3.15 %) and at day 28 (DRM 3.5 %) post-treatment. In conclusion, DRM treatment could offer some therapeutic advantages in field situations where IVM fails to control mange. Depending on the level of susceptibility of the mite population, long-acting pharmaceutical formulations can be useful to control Psoroptic mange in cattle. The use of macrocyclic lactones for mange control in cattle should be based on appropriate diagnosis on each individual farm.

摘要

痒螨病会导致牛的生产力出现相关损失。大环内酯类药物是推荐用于控制该病的主要药物手段之一。当前这项工作的目的是比较伊维菌素(IVM)和多拉菌素(DRM)作为传统(1%)或长效(3.15 - 3.5%)注射剂给自然感染绵羊痒螨的牛给药后的药代动力学行为与有效性之间的关系。整个工作包括在商业肉牛养殖场(放牧系统)进行的三项试验(试验1、试验2和试验3)。在试验1中,将20头患有活动性螨病感染的放牧阉牛分为2组(n = 10),并以0.2mg/kg的剂量皮下注射(SC)IVM(1%)或DRM(1%)。在试验2中,将16头患有活动性螨病的放牧阉牛分为2组(n = 8),分别皮下注射IVM 1%(0.2mg/kg)或IVM 3.15%长效制剂(0.63mg/kg)。在试验3中,将2组感染螨病的阉牛(n = 8)分别皮下注射IVM 3.15%(0.63mg/kg)或DRM 3.5%(0.7mg/kg)。采集每个实验组的血样,并通过高效液相色谱法测量IVM/DRM浓度来估计药物的全身可用性。从每只动物身上采集皮肤刮片样本,并在治疗后14天、21天和28天对螨进行计数。在试验1中,与IVM(1.80)相比,DRM在第14天的螨密度评分显著更低(0.60)(P = 0.019)。根据临床治愈动物(螨呈阴性)的数量,DRM的疗效(80%)高于IVM(10%)(P < 0.05)。以AUC衡量的DRM全身暴露量比IVM高1.37倍。在试验2中,尽管长效(3.15%)制剂后的IVM暴露量比传统制剂(1%)显著更高,但两种治疗均未显著降低螨密度评分,两种IVM治疗后治愈动物的百分比在0%至37.5%之间。在试验3中,在治疗后第21天(IVM 3.15%)和第28天(DRM 3.5%)实现了100%的动物治愈。总之,在IVM无法控制螨病的现场情况下,DRM治疗可能具有一些治疗优势。根据螨种群的易感性水平,长效药物制剂可用于控制牛的痒螨病。在牛群中使用大环内酯类药物控制螨病应基于每个农场的适当诊断。

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