Borges F A, Silva H C, Buzzulini C, Soares V E, Santos E, Oliveira G P, Costa A J
CPPAR, Faculdade de Ciências Agrárias e Veterinárias, São Paulo State University, Via de acesso Prof. Paulo Donato Castellane, s/n, CEP 14884-900, Jaboticabal-SP, Brazil.
Vet Parasitol. 2008 Aug 17;155(3-4):299-307. doi: 10.1016/j.vetpar.2008.04.019. Epub 2008 May 10.
The present work aimed to evaluate the endectocide activity of a new injectable long-action formulation, containing ivermectin (IVM) and abamectin (ABA). In each one of the four experiments performed, the following groups were formed: group I: 2.25% IVM (450 microg/kg)+1.25% ABA (250 microg/kg), group II: 3.15% IVM (630 microg/kg) and group III: control. Eighteen bovine naturally infected by gastrointestinal nematoda were selected for anthelmintic evaluation and necropsied on posttreatment day (PTD) 14 to estimate the total parasitic burden. For the Rhipicephalus (Boophilus) microplus field trial, 30 bovine were selected by means of counts of semi-engorged R. (B.) microplus and the therapeutic and residual efficacy evaluated by tick counts on PTDs 1, 3, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 77, 84 and 91. In the stall test, 15 calves were artificially infested with 5000 R. (B.) microplus (Mozzo strain) larvae three times a week and daily collections of all the engorged female ticks detached from each calf were performed until the PTD 80. Forty bovine naturally infected with Dermatobia hominis larvae were selected and the number of larvae was counted by visual and tactile inspection on PTDs 3, 7, 14, 28, 35, 49, 63, 77, 91 and 105. In this trial, a formulation containing 1% doramectin (200 microg/kg) was also used. IVM+ABA formulation and 3.15% IVM eliminated four of the eight species of nematode identified. The anthelmintic efficacy of the avermectins association against Haemonchus placei, Cooperia spatulata and C. punctata was 89.64%, 98.84% and 97.69%, while 3.15% IVM achieved 30.98%, 84.79% and 75.56%, respectively. The two formulations evaluated showed reduced acaricide action on the PTD 1 and 3, reaching high efficacy percentages from PTD 14 onward. The IVM+ABA showed efficacy above 95% in the period between PTDs 21 and 49. In the stall test, it observed no difference (P>0.05) between the two formulations regarding the R. (B.) microplus counts during the entire evaluation period. IVM+ABA reduced the number of ticks from the PTD 1 to 77 (P<0.05) and 3.15% IVM reduced (P<0.05) the tick number from PTD 4 up to PTD 80. The three endectocides showed no difference (P>0.05) regarding the number of D. hominis larvae and prevented this parasite reestablishment until PTD 105. These results indicate that the IVM+ABA association showed higher anthelmintic activity and similar efficacy against arthropods to the formulation containing 3.15% IVM.
本研究旨在评估一种含有伊维菌素(IVM)和阿维菌素(ABA)的新型注射用长效制剂的体内外寄生虫驱杀活性。在进行的四项实验中,每组均分为以下几组:第一组:2.25% IVM(450微克/千克)+1.25% ABA(250微克/千克);第二组:3.15% IVM(630微克/千克);第三组:对照组。选择18头自然感染胃肠道线虫的牛进行驱虫效果评估,并在治疗后第14天(PTD 14)进行剖检,以估计总寄生虫负荷。对于微小牛蜱田间试验,通过计数半饱血的微小牛蜱选择30头牛,并在PTD 1、3、7、14、21、28、35、42、49、56、63、70、77、84和91天通过蜱计数评估治疗效果和残留效果。在畜栏试验中,每周三次给15头小牛人工感染5000只微小牛蜱(莫佐菌株)幼虫,并每天收集从每头小牛身上脱落的所有饱血雌蜱,直至PTD 80。选择40头自然感染人皮蝇幼虫的牛,并在PTD 3、7、14、28、35、49、63、77、91和105天通过视觉和触觉检查计算幼虫数量。在该试验中,还使用了一种含有1%多拉菌素(200微克/千克)的制剂。IVM+ABA制剂和3.15% IVM消除了已鉴定的八种线虫中的四种。阿维菌素组合对牛血矛线虫、有齿库珀线虫和点状库珀线虫的驱虫效果分别为89.64%、98.84%和97.69%,而3.15% IVM分别为30.98%、84.79%和75.56%。评估的两种制剂在PTD 1和3时杀螨作用降低,从PTD 14起达到高疗效百分比。IVM+ABA在PTD 21至49期间显示出高于95%的疗效。在畜栏试验中,在整个评估期间,两种制剂在微小牛蜱计数方面没有差异(P>0.05)。IVM+ABA从PTD 1至77减少了蜱的数量(P<0.05),3.15% IVM从PTD 4至PTD 80减少了蜱的数量(P<0.05)。三种体内外寄生虫驱杀剂在人皮蝇幼虫数量方面没有差异(P>0.05),并在PTD 105之前防止了这种寄生虫的重新感染。这些结果表明,IVM+ABA组合显示出更高的驱虫活性,并且对节肢动物的疗效与含有3.15% IVM 的制剂相似。