O'Brien D J, Forbes A B, Pitt S R, Baggott D G
Central Veterinary Research Laboratory, Castleknock, Dublin, Ireland.
Vet Parasitol. 1999 Aug 16;85(1):79-85. doi: 10.1016/s0304-4017(99)00109-0.
In an experiment to determine the therapeutic efficacy of an ivermectin intraruminal controlled-release (CR) bolus, 14 mixed breed sheep of one lot were infested with Psoroptes ovis and subsequently divided into two groups of seven. In one of these groups each sheep received one ivermectin CR bolus appropriate to its weight, the other group remained as an untreated control. All mites were eliminated from the group receiving the bolus while the control group remained infested, the disease progressed, and all but one sheep required treatment for psoroptic mange before the end of the experimental period. A second lot of 14 sheep, free from P. ovis, were divided equally into two groups to determine the prophylactic efficacy of the ivermectin CR bolus. In one group, each sheep was given an ivermectin CR bolus according to body weight and the sheep in the other group received no medication and served as untreated controls. Twenty-one days later two sheep infested with psoroptic mange were introduced into each of the groups. These donor sheep were removed 10 days later. The group treated with the ivermectin CR bolus remained mange-free and did not harbour any mites. All of the sheep in the control group developed psoroptic mange and required treatment to control the infestation at the end of the experimental period. Sheep that received the ivermectin CR bolus had greater mean weight gains than the control groups in these experiments. The ivermectin CR bolus releases a minimum dose of 20 microg ivermectin kg/day for 100 days: this prolonged activity should prove a valuable asset for the treatment and control of psoroptic mange in sheep.
在一项确定伊维菌素瘤胃内控释(CR)丸剂治疗效果的实验中,一批14只混种绵羊感染了绵羊痒螨,随后被分成两组,每组7只。其中一组的每只绵羊都接受了一剂与其体重相适应的伊维菌素CR丸剂,另一组作为未治疗的对照组。接受丸剂治疗的组中所有螨虫都被清除,而对照组仍受感染,病情进展,在实验期结束前,除一只绵羊外,所有绵羊都需要治疗绵羊痒螨病。另一批14只未感染绵羊痒螨的绵羊被平均分成两组,以确定伊维菌素CR丸剂的预防效果。一组中,每只绵羊根据体重给予一剂伊维菌素CR丸剂,另一组的绵羊不接受药物治疗,作为未治疗的对照组。21天后,将两只感染绵羊痒螨病的绵羊引入每组。10天后将这些供体绵羊移走。接受伊维菌素CR丸剂治疗的组没有感染痒螨病,也没有螨虫寄生。对照组的所有绵羊都患上了绵羊痒螨病,在实验期结束时需要治疗以控制感染。在这些实验中,接受伊维菌素CR丸剂的绵羊平均体重增加量比对照组更大。伊维菌素CR丸剂在100天内每天释放至少20微克伊维菌素/千克:这种延长的活性对于治疗和控制绵羊痒螨病应是一项宝贵的资产。