Monahan C M, Chapman M R, French D D, Taylor H W, Klei T R
Department of Veterinary Microbiology and Parasitology, School of Veterinary Medicine, Louisiana State University, Baton Rouge 70803, USA.
Vet Parasitol. 1995 Oct;59(3-4):241-8. doi: 10.1016/0304-4017(94)00762-2.
Moxidectin was tested as an oral gel formulation during a controlled test performed to evaluate dosages against equine gastrointestinal parasites. Four groups of ten ponies were used. Ponies ranged from 1 to 20 years of age and were naturally infected in southern Louisiana or Mississippi. Fecal exams and fecal cultures were performed on all ponies to determine the strongyle egg counts and the percent distributions of large and small strongyles. Following these determinations, ponies were allocated to replicates of four ponies to provide an even distribution of strongyle infection, age, weight and gender. Members of each replicate were then randomly assigned to one of four treatment groups. The doses tested were 300, 400 and 500 micrograms kg-1 body weight. The oral gel vehicle alone served as control. Treatments were administered behind the tongue and the ponies were observed continuously for 4 h for any adverse reactions; thereafter, ponies were observed at least twice daily. Necropsy examinations were performed 14 days post-treatment for the recovery and identification of any parasites present. Moxidectin, at all doses tested, was 100% efficacious against adults of Strongylus vulgaris, Strongylus edentatus, Triodontophorus spp. and 22 species of small strongyles. Moxidectin was also 100% efficacious against larvae of Strongylus edentatus and Oxyuris equi, greater than 94% efficacious against Strongylus vulgaris larvae and Oxyuris equi adults at 14 days post-treatment. Moxidectin proved highly efficacious against luminal small strongyle larvae (> 99.9% against L4 and > 92% against L3) and moxidectin demonstrated some efficacy against encysted small strongyle larvae as well.(ABSTRACT TRUNCATED AT 250 WORDS)
在一项为评估抗马胃肠道寄生虫剂量而进行的对照试验中,莫昔克丁以口服凝胶制剂的形式进行了测试。使用了四组,每组十匹小马。小马年龄在1至20岁之间,在路易斯安那州南部或密西西比州自然感染。对所有小马进行粪便检查和粪便培养,以确定圆线虫卵计数以及大小圆线虫的百分比分布。在进行这些测定之后,将小马分配到每组四匹的重复组中,以使圆线虫感染、年龄、体重和性别均匀分布。然后将每个重复组的成员随机分配到四个治疗组之一。测试的剂量为300、400和500微克/千克体重。仅口服凝胶载体用作对照。在舌后给予治疗,连续观察小马4小时,观察是否有任何不良反应;此后,每天至少观察小马两次。在治疗后14天进行尸检,以恢复和鉴定任何存在的寄生虫。在所测试的所有剂量下,莫昔克丁对普通圆线虫、无齿圆线虫、三齿圆线虫属的成虫以及22种小圆线虫均有100%的疗效。莫昔克丁对无齿圆线虫和马尖尾线虫的幼虫也有100%的疗效,在治疗后14天对普通圆线虫幼虫和马尖尾线虫成虫的疗效大于94%。莫昔克丁对肠腔内小圆线虫幼虫具有高效(对L4的疗效>99.9%,对L3的疗效>92%),并且莫昔克丁对包囊小圆线虫幼虫也有一定疗效。(摘要截短为250字)