首页> 外文期刊>Veterinary Parasitology >Terpenes on Rhipicephalus (Boophilus) microplus: Acaricidal activity and acetylcholinesterase inhibition
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Terpenes on Rhipicephalus (Boophilus) microplus: Acaricidal activity and acetylcholinesterase inhibition

机译:Rapicephalus(Boophilus)微粒:Agaricidal活性和乙酰胆碱酯酶抑制作用

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摘要

The Rhipicephalus (Boophilus) microplus tick is the main ectoparasite of cattle in tropical and subtropical regions worldwide. Resistance to chemical acaricides has become widespread affirming the need for new drugs to tick control. Terpenes have become a promising alternative for cattle tick control, however the mechanism of action of these compounds is still controversial. Inhibition of acetylcholinesterase (AChE) is a well established mechanism of action of organophosphate and carbamate acaricides, but the possible action of terpenes on tick AChEs has seldom been studied in resistant and sensitive strains of R. (B.) microplus. The aim of the present study was to evaluate terpene inhibition of AChE from resistant and sensitive strains of R. (B.) microplus in correlation with their acaricidal activity. Among the terpenes used in the present study, p-cymene, thymol, carvacrol, and citral displayed acaricidal activity with LC50 of 1.75, 1.54, 1.41, and 0.38 mg.mL(-1) for the susceptible strain, and LC50 of 1.40, 1.81, 1.10, and 1.13 mg.mL(-1) for the resistant strain. Thymol and carvacrol inhibited the AChE of the susceptible strain larvae with IC50 of 0.93 and 0.04 mg.mL(-1), respectively. The IC50 exhibited by eucalyptol, carvacrol and thymol for AChE of the resistant strain larvae were 0.36, 0.28, and 0.13 mg.mL(-1), respectively. This was the first study to investigate the action of terpenes on AChE from susceptible and resistant R. (B.) microplus. As not all terpenes with acaridical activity showed AChE inhibition, the participation of AChE in the acaricidal activity of terpenes needs further investigation.
机译:Rapicephalus(Boophilus)Microplus Tick是全球热带和亚热带地区牛的主要异位岩。抗化学杀螨剂的抗性已普遍肯定需要新药来蜱控制。 Terpenes已成为牛蜱控制的有希望的替代方案,但这些化合物的作用机制仍存在争议。抑制乙酰胆碱酯酶(ACHE)是成立的有机磷酸盐和氨基甲酸氨基甲酰胺作用的良好作用机制,但萜烯对蜱酸的可能作用很少已经在R.(B.)微片的抗性和敏感菌株中进行了研究。本研究的目的是评估与其杀螨活性相关的抗抗性和敏感菌株的抗脂肪和敏感菌株。在本研究中使用的萜烯中,P-CYMENE,胸腺酚,碳酸和柠檬酸,LC50为1.75,1.54,1.41和0.38mg.ML(-1)的敏感活性,用于易感应变,LC50为1.40, 1.81,1.10和1.13 mg.ml(-1)用于抗性应变。胸腺和胰酸蟑螂分别抑制了IC50为0.93和0.04mg.ml(-1)的易感菌株幼虫的疼痛。桉树术,钙吡咯和抗抗性菌株幼虫的钙钨醇的IC50分别为0.36,0.28和0.13mg.ml(-1)。这是第一项研究,以研究Terpenes对来自易感和抗性R.(B.)微片段疼痛的作用。并非所有具有Acaridical活性的Terpenes都表现出疼痛的抑制,疼痛在Terpenes的Acaricidal活性中的参与需要进一步调查。

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