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Mechanism of Selective Actions of Neonicotinoids on Insect Nicotinic Acetylcholine Receptors

机译:Neonicotinoids对昆虫烟碱乙酰胆碱受体的选择性作用

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Neonicotinoid insecticides act selectively on insect nicotinic acetylcholine receptors (nAChRs), but little is known about the mechanism of selectivity. To elucidate the mechanism, structural features of neonicotinoids and insect nAChRs J contributing to this selectivity have been examined. Using molecular-oribital calculations, electrostatic interactions and hydrogen-bond formation of neonicotinoids with insect nAChRs were postulated to contribute to the selectivity of neonicotinoid-nAChR interactions. Also, the use of voltage-clamp electrophysiology combined with molecular biology showed that replacement of the vertebrate ct4 subunit in the a4|32 nAChR by Drosophila a subunits and mutation to basic residues of an amino acid in loop D of the a7 nAChR enhanced neonicotinoid sensitivity of the nAChRs. These findings suggest important roles for a and non-oc subunits in the selective actions of neonicotinoids on insect nAChRs.
机译:Neonicotinoid杀虫剂在昆虫烟碱乙酰胆碱受体(NACHRS)上有选择性地作用,但是关于选择性的机制很少。为了阐明促进新烟蛋白和昆虫NACHRS J的机制,已经研究过促进促进这种选择性的昆虫。利用分子值计算,假设用昆虫NACHRS的静电相互作用和氢键形成昆虫丁醇的形成,有助于Neonicotinoid-NACHR相互作用的选择性。此外,使用电压 - 钳位电生理学与分子生物学结合的使用表明,在A7 NACHR的环D的环D的氨基酸的亚基和突变中,将脊椎动物CT4亚基在A7 NACHR增强的Neonicotinoid敏感度的环D中的突变中置换NACHRS。这些研究结果表明,在昆虫NACHRS的Neonicotinoids选择性作用中的A和非OC亚基的重要作用。

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