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A novel action of highly specific acaricide; bifenazate as a synergist for a GABA-gated chloride channel of Tetranychus urticae [Acari: Tetranychidae]

机译:高特异性杀螨剂的新作用;联苯甲酸盐作为Tetranychus urticae的GABA门控氯化物通道的增效剂[Acari:Tetranychidae]

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摘要

Bifenazate is a very selective acaricide that controls the spider mite, Tetranychus urticae. Bifenazate is the first example of a carbazate acaricide. Its mode of action remains unclear. Bifenazate and its active metabolite diazene induce paralysis in spider mites, suggesting that they may act on the nervous system. Here we have employed a homologue (TuGABAR) of RDL (Resistance to dieldrin), a subunit of ionotropic γ-aminobutyric acid (GABA) receptor, from T. urticae to investigate the action of bifenazate and its active metabolite diazene on this receptor function. Although neither acaricide showed a GABA agonist action, 30μM of bifenazate or diazene significantly enhanced the GABA-induced response of TuGABAR in a dose-dependent manner, shifting the EC 50 of GABA from 24.8μM to 4.83μM and 10.8μM, respectively. This action demonstrates a positive allosteric modulator effect of bifenazate on T. urticae GABA receptors. This synergistic action is likely the result of bifenazate binding to a site distinct from that of the GABA binding site causing a conformational change that affects the magnitude of the GABA response. Precisely how the observed GABA synergist action correlates with the acaricidal activity of bifenazate, if at all, has yet to be determined.
机译:Bifenazate是一种非常有选择性的杀螨剂,可控制红蜘蛛Tetranychus urticae。联苯肼酯是氨基甲酸酯类杀螨剂的第一个例子。其作用方式仍不清楚。联苯吡唑及其活性代谢物重氮诱导红蜘蛛麻痹,表明它们可能作用于神经系统。在这里,我们采用了RDL(对狄氏剂的抵抗力)的同系物(TuGABAR)(一种离子型γ-氨基丁酸(GABA)受体的亚单位),来自荨麻疹,来研究联苯肼酯及其活性代谢物重氮对该受体功能的作用。尽管两种杀螨剂均未显示出GABA激动剂的作用,但30μM的联苯吡酯或二氮烯以剂量依赖的方式显着增强了GABA诱导的TuGABAR反应,使GABA的EC 50分别从24.8μM变为4.83μM和10.8μM。该作用表明联苯吡酯对荨麻疹GABA受体具有积极的变构调节作用。这种协同作用可能是联苯芬酸酯结合至不同于GABA结合位点的位点的结果,导致构象变化影响了GABA反应的幅度。确切地说,观察到的GABA协同作用与联苯吡唑的杀螨活性之间如何相关,尚待确定。

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