Lok James B, Washabau Robert J, Heaney Kathleen, Nolan Thomas J, Hendrick Mattie J, Neumann Norwood R, Ulrich Michael
Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Vet Parasitol. 2005 Oct 24;133(2-3):233-41. doi: 10.1016/j.vetpar.2005.06.019.
The purpose of this study was to assess the efficacy of moxidectin sustained release injectable for dogs (moxidectin SR, Fort Dodge Animal Health) in protecting growing puppies from experimental infection with the heartworm, Dirofilaria immitis, six months after treatment. The study involved 27 puppies, approximately 12 weeks of age at the beginning of the study, with nine puppies in each of three size classes. The small breed class included eight Pekingese and one purpose-bred small breed mongrel; the medium breed class included nine purpose-bred mongrels, and the large breed class included nine puppies with an anticipated adult weight >or=30-35 kg. Both genders were included with no attempt made to have equal numbers of male and female puppies. Puppies were blocked by weight within each size class and randomly assigned to three treatment groups of nine dogs. On Day 0, pups in two groups were injected subcutaneously with moxidectin SR, dosed to deliver 0.17 mg moxidectin/kg b.w. The third group was injected with sterile saline. Personnel making observations were blinded to the treatment status of the animals. Following treatment, puppies were observed for signs of adverse local and systemic reactions. Puppy weights and serum moxidectin levels were also monitored. On Day 180, puppies in all treatment groups were inoculated subcutaneously with 50 third-stage larvae of D. immitis. On Days 348 and 349, puppies were euthanatized and necropsied. Hearts and lungs were examined for adult heartworms. All animals in the saline control group were infected with an arithmetic mean of 39.22 adult heartworms each. Seventeen of 18 dogs in the moxidectin SR-treated groups were uninfected. One treated puppy was infected with a single adult heartworm. This infected individual was from the large breed size class and had the second highest percent increase in body weight. Based on arithmetic means, the heartworm recovery from all treated puppies represents a 99.86% reduction relative to the saline control. There were no adverse local or systemic reactions to treatment in any animal.
本研究的目的是评估犬用莫昔克丁缓释注射液(莫昔克丁SR,法玛西亚动物保健公司)在治疗六个月后,对生长中的幼犬预防感染犬恶丝虫实验感染的效果。该研究涉及27只幼犬,研究开始时约12周龄,分为三个体型组,每组九只。小型犬组包括八只北京犬和一只专门培育的小型杂种犬;中型犬组包括九只专门培育的杂种犬,大型犬组包括九只预期成年体重≥30 - 35千克的幼犬。两个性别均有纳入,未试图使雄性和雌性幼犬数量相等。幼犬在每个体型组内按体重进行分组,并随机分配到三个治疗组,每组九只犬。在第0天,两组幼犬皮下注射莫昔克丁SR,剂量为每千克体重0.17毫克莫昔克丁。第三组注射无菌生理盐水。进行观察的人员对动物的治疗状态不知情。治疗后,观察幼犬有无局部和全身不良反应的迹象。还监测幼犬体重和血清莫昔克丁水平。在第180天,所有治疗组的幼犬皮下接种50条犬恶丝虫三期幼虫。在第348天和第349天,对幼犬实施安乐死并进行尸检。检查心脏和肺部有无成年心丝虫。生理盐水对照组的所有动物均感染了成年心丝虫,算术平均值为每只39.22条。莫昔克丁SR治疗组的18只犬中有17只未感染。一只接受治疗的幼犬感染了一条成年心丝虫。这只受感染的个体来自大型犬组,体重增加百分比第二高。基于算术平均值,所有接受治疗的幼犬的心丝虫感染率相对于生理盐水对照组降低了99.86%。任何动物在治疗过程中均未出现局部或全身不良反应。