新烟碱制剂Actara®的生态(毒理学)评价,以拟涡虫为模式生物

Rone S. Barbosa, Eliane Aparecida Rotili, Amanda Magda Almeida Santos, Fabianne Ribeiro, A. Dornelas, D. Pereira, G. Cavallini, A. Soares, R. Sarmento, C. Gravato
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引用次数: 1

摘要

新烟碱类农药是世界上商业化程度最高的一类农药。它们在农业中的应用旨在通过一种不针对目标物种的系统作用模式来控制害虫。我们的研究旨在评估杀虫剂Actara®[有效成分噻虫嗪(TMX)]对非目标物种Girardia tigrina的影响。因此,评估了急性和亚致死终点,如死亡率、摄食活动、运动和行为生物标志物。Actara®对原虫Girardia tigrina具有较低的毒性,96 h LC50值为77.6 mg TMX·L−1 (95% ci: 74.1 ~ 81.2 mg TMX·L−1;R2 = 0.85)。在亚致死水平下,Actara®对暴露后24和48 h的涡虫光感受器和耳廓的再生没有影响(NOEC > 7.8 mg TMX·L−1)。Actara®可显著提高涡虫的取食率,但仅在最高测试浓度(LOEC = 7.8 mg TMX·L−1)时有效。与其他淡水物种相比,涡虫对活性成分TMX的敏感性较低。这可能是由于涡虫中存在高比例的乙酰胆碱受体亚型,表现出对乙酰胆碱部分激动剂TMX的低结合亲和力。比较Actara®与其他配方对涡虫的影响,可能有助于我们理解其他未知成分如何改变涡虫对这些物质的吸收和生物利用度,以及解毒能力,所有这些都会影响毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eco(toxicological) Assessment of the Neonicotinoid Formulation Actara® Using Planarian Girardia tigrina as Model Organism
Neonicotinoid pesticides are one of the most commercialized groups worldwide. Their application in agriculture aims to control pests through a systemic mode of action which is not specific to target species. Our study aimed to evaluate the effects of the insecticide Actara® [active ingredient thiamethoxam (TMX)] on a non-target species, Girardia tigrina. Therefore, acute and sublethal endpoints, such as mortality, feeding activity, locomotion and behavioral biomarkers were assessed. Actara® exerted low toxicity towards the planarian Girardia tigrina, showing a 96 h LC50 value of 77.6 mg TMX·L−1 (95% C.I: 74.1–81.2 mg TMX·L−1; R2 = 0.85). At the sublethal level, Actara® exerted no effect on regeneration of photoreceptors and auricles of planarians after 24 and 48 h post-exposure (NOEC > 7.8 mg TMX·L−1). The feeding rate of planarians was significantly increased by Actara®, but only at the highest tested concentration (LOEC = 7.8 mg TMX·L−1). Planarians showed to be less sensitive to the active ingredient TMX compared to other freshwater species. This might be explained by the presence of a high proportion of sub-types of acetylcholine receptors in planarians, exhibiting low binding affinity sites for TMX, an acetylcholine partial agonist. The comparison between effects induced by Actara® with the ones caused by other formulations, in planarians, might support our understanding of how other unknown ingredients can modify the uptake, and bioavailability of such substances, as well as the detoxification capacity of planarians, all of which influences toxicity.
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