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首页> 外文期刊>Journal of pesticide science >Actions of imidacloprid,clothianidin and related neonicotinoids on nicotinic acetylcholine receptors of American cockroach neurons and their relationships with insecticidal potency
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Actions of imidacloprid,clothianidin and related neonicotinoids on nicotinic acetylcholine receptors of American cockroach neurons and their relationships with insecticidal potency

机译:吡虫啉,可比尼丁和相关新烟碱类对美国蟑螂神经元烟碱乙酰胆碱受体的作用及其与杀虫力的关系

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摘要

The actions of neonicotinoid insecticides on nicotinic acetylcholine receptors(nAChRs)in the terminal abdominal ganglion neurons of the American cockroach were investigated using whole-cell patch-clamp electrophysiol-ogy.Neonicotinoids possessing a nitromethylene group showed higher agonist affinity than the corresponding ni-troimine analogues,whereas compounds with an acyclic guanidine moiety showed greater agonist efficacy than the corresponding cyclic compounds.Imidacloprid showed the lowest agonist efficacy of all neonicotinoids and low concentrations of imidacloprid attenuated acetylcholine-induced currents.However,such blocking actions were minimal with other neonicotinoids.The diverse actions of neonicotinoids on nAChRs,combined with target accessibility based on hydrophobicity,appears to account for their insecticidal potency on cockroaches measured in the presence of metabolic inhibitors.
机译:使用全细胞膜片钳电生理-糖醇研究了新蟑螂类杀虫剂对美国蟑螂末端腹神经节神经元中烟碱样乙酰胆碱受体(nAChRs)的作用。具有亚硝基基团的新烟碱类化合物的激动剂亲和力高于相应的硝化亚硝基亚胺。类似物,而具有无环胍部分的化合物显示出比相应的环状化合物更高的激动剂效力。吡虫啉显示出所有新烟碱类药物的激动剂功效最低,吡虫啉减毒乙酰胆碱诱导的电流浓度低,但是,其他新烟碱类药物的阻滞作用很小。新烟碱类化合物对nAChRs的不同作用,加上基于疏水性的靶标可及性,似乎说明了它们在代谢抑制剂存在下对蟑螂的杀虫力。

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