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单萜的杀软体动物活性及其对中间宿主光滑双脐螺乙酰胆碱酯酶活性抑制的影响。

Molluscicidal activity of monoterpenes and their effects on inhibition of acetylcholinesterase activity on Biomphalaria glabrata, an intermediate host of Schistosoma mansoni.

机构信息

Graduate Program in Biotechnology - Renorbio, Federal University of Maranhão, 65080-805, São Luís, MA, Brazil.

Graduate Program in Health Sciences, Federal University of Maranhão, 65080-805, São Luís, MA, Brazil.

出版信息

Acta Trop. 2021 Nov;223:106089. doi: 10.1016/j.actatropica.2021.106089. Epub 2021 Aug 11.

Abstract

The molluscicidal action of essential oils have been attributed to the most prevalent terpene compounds. However, molluscicidal properties, mode of action, and toxicity to non-target organisms remain unclear. In this study, the molluscicidal potential of four monoterpenes (camphor, thymol, α-pinene, and 1,8-cineole) against the snail Biomphalaria glabrata, an intermediate host of Schistosoma mansoni, was analyzed. The molluscicide activity of each monoterpene was assessed by the standardized test of the World Health Organization (WHO) and the monoterpenes considered active against B. glabrata were analyzed as inhibitors of the enzymatic activity of acetylcholinesterase (AChE) extracted from snails. In addition, acute toxicity to non-target organisms was assessed against Danio rerio fish. The results show that camphor and 1,8-cineole monoterpenes did not induce snail mortality. Thymol and α-pinene were active against B. glabrata, inducing mortality in concentration-dependent patterns and showing a lethal effect in concentrations compatible with that recommended by the WHO (LC of 7.11 and LC 10.34 μg ∙ mL, respectively). The toxic action of thymol and α-pinene on snails indicates that these monoterpenes may account for or largely contribute to the molluscicidal activity of essential oils that contain them as major compounds. Thymol and α-pinene inhibit the AChE of B. glabrata at concentrations higher than those used in the molluscicide test. These monoterpenes show low toxicity to non-target organisms compared to the commercial molluscicide niclosamide. Knowledge about monoterpene toxicity against B. glabrata contributes to its potential use in molluscicidal formulations and in alternatives to the control of snails that host intermediate S. mansoni, a crucial action in the prevention and transmission of schistosomiasis, a neglected tropical disease.

摘要

精油的杀软体动物作用归因于最普遍的萜烯化合物。然而,杀软体动物特性、作用方式和对非靶标生物的毒性仍然不清楚。在这项研究中,分析了四种单萜(樟脑、百里香酚、α-蒎烯和 1,8-桉叶油醇)对中间宿主曼氏血吸虫的福寿螺的杀软体动物潜力。通过世界卫生组织(WHO)的标准化测试评估每种单萜的杀软体动物活性,并且将被认为对 B. glabrata 有活性的单萜分析为从蜗牛中提取的乙酰胆碱酯酶(AChE)的抑制剂。此外,还评估了对非靶标生物的急性毒性。结果表明,樟脑和 1,8-桉叶油醇单萜没有引起蜗牛死亡。百里香酚和α-蒎烯对 B. glabrata 具有活性,以浓度依赖性方式诱导死亡率,并在与 WHO 推荐浓度(LC 分别为 7.11 和 LC 10.34μg·mL)相容的浓度下表现出致死作用。百里香酚和α-蒎烯对蜗牛的毒性作用表明,这些单萜可能是或在很大程度上导致含有它们作为主要化合物的精油的杀软体动物活性。百里香酚和α-蒎烯在高于杀软体动物试验中使用的浓度下抑制 B. glabrata 的 AChE。与商业杀软体动物药硝氯酚相比,这些单萜对非靶标生物的毒性较低。关于单萜对 B. glabrata 的毒性的知识有助于将其用于杀软体动物制剂和替代控制作为中间宿主的蜗牛,这是预防和传播被忽视的热带病血吸虫病的关键行动。

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