Cruz Paula Barroso, Barbosa Alan Franco, Zeringóta Viviane, Melo Diego, Novato Tatiane, Fidelis Queli Cristina, Fabri Rodrigo Luiz, de Carvalho Mário Geraldo, Oliveira Sabaa-Srur Armando Ubirajara, Daemon Erik, Monteiro Caio Márcio Oliveira
Programa de Pós-graduação em Ciências Biológicas - Comportamento e Biologia Animal da Universidade Federal de Juiz de Fora- Rua José Lourenço Kelmer, s/n - Campus Universitário - Bairro São Pedro - Juiz de Fora - MG, 36036-900, Brazil.
Programa de Pós-Graduação em Ciência e Tecnologia de Alimentos da Universidade Federal Rural do Rio de Janeiro, Rodovia BR 465 - Km 7, Seropédica - RJ, 23897-000, Brazil; Instituto Federal de Educação, Ciência e Tecnologia de Mato Grosso - Campus Sorriso, Avenida dos Universitários, 799, Bairro Santa Clara, Sorriso-MT, 78.890-000, Brazil.
Vet Parasitol. 2016 Sep 15;228:137-143. doi: 10.1016/j.vetpar.2016.08.026. Epub 2016 Sep 1.
We evaluated the acaricidal activity of Acmella oleracea methanol extract and spilanthol on Rhipicephalus microplus and Dermacentor nitens. The extract was made through maceration with methanol. From this extract, a dichloromethane fraction with 99% spilanthol was obtained and tested on R. microplus larvae and engorged females and D. nitens larvae. For evaluation against larvae, the modified larval packet test was used, and both the methanol extract and dichloromethane fraction were tested at concentrations of 0.2-50mg/mL. The modified larval packet test was also used in the lethal time (LT) test, with the methanol extract at a concentration of 12.5mg/mL and the percentage mortality was assessed after 15, 30, 45, 60, 75, 90, 120min and 24h. The 50% lethal time calculation (LT) was performed in this test. The engorged female test was performed with R. microplus only, at concentrations of 25-200mg/mL for methanol extract and 2.5-20.0mg/mL for spilanthol. The methanol extract caused 100% mortality of the R. microplus and D. nitens larvae at concentrations of 3.1 and 12.5mg/mL, respectively. Spilanthol resulted in 100% mortality of R. microplus larvae at concentration of 1.6mg/mL and of D. nitens at 12.5mg/mL. In the lethal time assay using the methanol extract, the mortality rate was 100% for R. microplus and D. nitens larvae after 120min and 24h, with LT values of 38 and 57min, respectively. In the test of females, the egg mass weight and the hatching percentage of the groups treated with concentrations equal to or higher than 50.0mg/mL of methanol extract were significantly reduced (p<0.05), while for spilanthol, the reduction of the egg mass weight and hatching percentage occurred from concentrations of 10.0mg/mL and 2.5mg/mL, respectively. Females treated with 200.0mg/mL of extract died before starting oviposition, resulting in 100% effectiveness, while the best efficacy for spilanthol was 92.9% at a concentration of 20.0mg/mL. Thus we conclude that the methanol extract of A. oleracea and spilanthol have acaricidal activity against R. microplus and D. nitens.
我们评估了金纽扣甲醇提取物和毛果芸香碱对微小扇头蜱和热带血蜱的杀螨活性。该提取物通过用甲醇浸渍制备。从该提取物中获得了含99%毛果芸香碱的二氯甲烷馏分,并对微小扇头蜱幼虫、饱血雌蜱和热带血蜱幼虫进行了测试。为了评估对幼虫的作用,使用了改良的幼虫包囊试验,甲醇提取物和二氯甲烷馏分均在0.2 - 50mg/mL的浓度下进行测试。改良的幼虫包囊试验也用于致死时间(LT)试验,甲醇提取物浓度为12.5mg/mL,在15、30、45、60、75、90、120分钟和24小时后评估死亡率。在该试验中进行了50%致死时间计算(LT)。饱血雌蜱试验仅对微小扇头蜱进行,甲醇提取物浓度为25 - 200mg/mL,毛果芸香碱浓度为2.5 - 20.0mg/mL。甲醇提取物在浓度分别为3.1mg/mL和12.5mg/mL时,导致微小扇头蜱和热带血蜱幼虫100%死亡。毛果芸香碱在浓度为1.6mg/mL时导致微小扇头蜱幼虫100%死亡,在12.5mg/mL时导致热带血蜱100%死亡。在使用甲醇提取物的致死时间试验中,微小扇头蜱和热带血蜱幼虫在120分钟和24小时后的死亡率均为100%,LT值分别为38分钟和57分钟。在雌蜱试验中,用浓度等于或高于50.0mg/mL甲醇提取物处理的组,卵块重量和孵化率显著降低(p<0.05),而对于毛果芸香碱,卵块重量和孵化率分别从10.0mg/mL和2.5mg/mL的浓度开始降低。用200.0mg/mL提取物处理的雌蜱在开始产卵前死亡,有效率达100%,而毛果芸香碱在浓度为20.0mg/mL时的最佳疗效为92.9%。因此,我们得出结论,金纽扣甲醇提取物和毛果芸香碱对微小扇头蜱和热带血蜱具有杀螨活性。