Silver Kristopher S, Du Yuzhe, Nomura Yoshiko, Oliveira Eugenio E, Salgado Vincent L, Zhorov Boris S, Dong Ke
Department of Anatomy and Physiology, Kansas State University, Manhattan, Kansas, USA.
Department of Entomology, Neuroscience and Genetics Programs, Michigan State University, East Lansing, Michigan, USA.
Adv In Insect Phys. 2014;46:389-433. doi: 10.1016/B978-0-12-417010-0.00005-7.
Voltage-gated sodium channels are critical for the generation and propagation of action potentials. They are the primary target of several classes of insecticides, including DDT, pyrethroids and sodium channel blocker insecticides (SCBIs). DDT and pyrethroids preferably bind to open sodium channels and stabilize the open state, causing prolonged currents. In contrast, SCBIs block sodium channels by binding to the inactivated state. Many sodium channel mutations are associated with knockdown resistance (kdr) to DDT and pyrethroids in diverse arthropod pests. Functional characterization of kdr mutations together with computational modelling predicts dual pyrethroid receptor sites on sodium channels. In contrast, the molecular determinants of the SCBI receptor site remain largely unknown. In this review, we summarize current knowledge about the molecular mechanisms of action of pyrethroids and SCBIs, and highlight the differences in the molecular interaction of these insecticides with insect versus mammalian sodium channels.
电压门控钠通道对于动作电位的产生和传播至关重要。它们是几类杀虫剂的主要作用靶点,包括滴滴涕、拟除虫菊酯和钠通道阻断剂杀虫剂(SCBIs)。滴滴涕和拟除虫菊酯优先结合开放的钠通道并稳定开放状态,导致电流延长。相比之下,SCBIs通过结合失活状态来阻断钠通道。许多钠通道突变与多种节肢动物害虫对滴滴涕和拟除虫菊酯的击倒抗性(kdr)相关。kdr突变的功能表征以及计算模型预测了钠通道上的双重拟除虫菊酯受体位点。相比之下,SCBI受体位点的分子决定因素在很大程度上仍然未知。在这篇综述中,我们总结了关于拟除虫菊酯和SCBIs作用分子机制的当前知识,并强调了这些杀虫剂与昆虫和哺乳动物钠通道分子相互作用的差异。