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Indoxacarb an oxadiazine insecticide blocks insect neuronal sodium channels

机译:茚达沙威一种恶二嗪类杀虫剂可阻断昆虫神经元钠通道

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摘要

class="enumerated" style="list-style-type:decimal">Decarbomethoxyllated JW062 (DCJW), the active component of a new oxadiazine insecticide DPX-JW062 (Indoxacarb), was tested on action potentials and the inward sodium current recorded from short-term cultured dorsal unpaired median neurones of the cockroach Periplaneta americana.Under whole-cell current-clamp conditions, 100 nM DCJW reduced the amplitude of action potentials and induced a large hyperpolarization of the resting membrane potential associated with a 41% increase in input resistance.In voltage-clamp, DCJW resulted in a dose-dependent inhibition (IC50 28 nM) of the peak sodium current. Based on IC50 values, the effect of DCJW was about 10 fold less potent than tetrodotoxin (TTX) but 1000 fold more potent than the local anaesthetic lidocaine. DCJW (100 nM) was without effect on activation properties of the sodium current, reversal potential, voltage dependence of sodium conductance and on both fast and slow steady-state inactivations.TTX (2 nM) resulted in 48% inhibition of the peak inward sodium current. Co-application of TTX (2 nM) with various concentrations of DCJW produced an additional inhibition of the peak inward current, indicating that the blocking actions of DCJW and TTX were distinct. Co-application of lidocaine (IC50 30 μM) with various concentrations of DCJW produced a reduction of the apparent potency of DCJW, suggesting that DCJW and lidocaine acted at the same site.DCJW (100 nM) did not affect inward calcium or outward potassium currents.This study describes, for the first time, the action on insect neuronal voltage-dependent sodium channels of Indoxacarb, a new class of insecticides.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 测试了新的恶二嗪类杀虫剂DPX-JW062(Indoxacarb)的活性成分脱甲氧甲氧基化的JW062(DCJW)的作用电位,并从美洲小Per的短期培养的背对未成对中位神经元记录了内向钠电流。 在全电池电流钳条件下,100 nM DCJW降低了动作电位的幅度,并导致静息膜电位发生大的超极化,从而使输入电阻增加了41%。 In电压钳DCJW导致钠电流峰值的剂量依赖性抑制(IC50 28 nM)。根据IC50值,DCJW的效力比河豚毒素(TTX)低约10倍,但效力比局部麻醉剂利多卡因高1000倍。 DCJW(100 nM)对钠电流的激活特性,反转电位,钠电导的电压依赖性以及快速和慢速稳态失活均没有影响。 TTX(2 nM)导致48 %抑制内向钠电流峰值。将TTX(2 nM)与各种浓度的DCJW共同使用会进一步抑制峰值内向电流,这表明DCJW和TTX的阻滞作用是不同的。利多卡因(IC50 30μM)与各种浓度的DCJW并用会降低DCJW的表观效力,这表明DCJW和利多卡因在同一部位起作用。 DCJW(100 nM)没有 该研究首次描述了新型杀虫剂茚虫威对昆虫神经元电压依赖性钠通道的作用。

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