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注射用和浇泼用莫西菌素对自然感染绵羊痒螨(蜱螨亚纲:痒螨科)的牛的田间药效

Field efficacy of injectable and pour-on moxidectin in cattle naturally infested with Psoroptes ovis (Acarina: Psoroptidae).

作者信息

Lonneux J F, Losson B

机构信息

Laboratory of Parasitology and Pathology of Parasitic Diseases, Faculty of Veterinary Medicine, University of Liège, Belgium.

出版信息

Vet Parasitol. 1992 Dec;45(1-2):147-52. doi: 10.1016/0304-4017(92)90037-a.

Abstract

Field efficacy of moxidectin, a macrocyclic lactone endectocide, was evaluated in cattle naturally infested with Psoroptes ovis. Three groups of six animals were used based on parasitological and clinical status. Group 1 animals received one subcutaneous injection of injectable moxidectin at 0.2 mg kg-1 body weight; Group 2 animals received topically one dose of 0.5 mg kg-1 body weight of pour-on moxidectin; Group 3 individuals remained untreated as controls. Efficacy was assessed by (a) taking skin samples from each animal on Days -4, 14, 28, 42 and 56 post-treatment (PT) and observing numbers of viable mite stages and species and (b) clinical examination of animals on Days 14, 28, 42 and 56 with the percentage of affected body surface calculated for each animal on Days -4, 28 and 56. Both formulations gave 100% efficacy as no live mites were found in Groups 1 or 2, 14, 28 and 56 days after treatment. Clinical indices showed a sharp decrease in the affected body surface area from a mean of 5.48% and 6.1% on Day -4 in Groups 1 and 2, respectively, to 0% in both groups on Days 28 and 56 PT. All untreated animals remained positive until Day 28. The clinical condition of the controls worsened rapidly during the experiment (mean clinical index: 2.87% and 13.05% on Days -4 and 28, respectively) and they were given an emergency treatment on Day 28. No side-effects were observed with either formulation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

大环内酯类体内外寄生虫杀虫剂莫昔克丁对自然感染绵羊痒螨的牛群的田间药效进行了评估。根据寄生虫学和临床状况,使用了三组,每组六只动物。第1组动物皮下注射一次莫昔克丁,剂量为0.2毫克/千克体重;第2组动物局部使用一剂剂量为0.5毫克/千克体重的莫昔克丁浇泼剂;第3组动物作为对照不进行治疗。通过以下方式评估药效:(a) 在治疗后第-4、14、28、42和56天从每只动物身上采集皮肤样本,观察存活螨的阶段和种类数量;(b) 在第14、28、42和56天对动物进行临床检查,并计算每只动物在第-4、28和56天受影响体表的百分比。两种制剂的药效均达100%,因为在治疗后14、28和56天,第1组和第2组均未发现活螨。临床指标显示,受影响的体表面积从第1组和第2组在第-4天分别平均为5.48%和6.1%急剧下降至治疗后第28天和56天两组均为0%。所有未治疗的动物直到第28天仍呈阳性。在实验期间,对照组的临床状况迅速恶化(第-4天和第28天的平均临床指标分别为2.87%和13.05%),并在第28天接受了紧急治疗。两种制剂均未观察到副作用。(摘要截选至250词)

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