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茚虫威杀虫剂对蟑螂神经元中两种钠通道亚型的阻断作用。

Block of two subtypes of sodium channels in cockroach neurons by indoxacarb insecticides.

作者信息

Zhao Xilong, Ikeda Tomoko, Salgado Vincent L, Yeh Jay Z, Narahashi Toshio

机构信息

Department of Molecular Pharmacology and Biological Chemistry, Northwestern University Medical School, Chicago, IL 60611, USA.

出版信息

Neurotoxicology. 2005 Jun;26(3):455-65. doi: 10.1016/j.neuro.2005.03.007. Epub 2005 Apr 26.

Abstract

Indoxacarb, a novel insecticide, and its decarbomethoxyllated metabolite, DCJW, are known to block voltage-gated Na(+) channels in insects and mammals, but the mechanism of block is not yet well understood. The present study was undertaken to characterize the action of indoxacarb and DCJW on cockroach Na(+) channels. Na(+) currents were recorded using the whole-cell patch clamp technique from neurons acutely dissociated from thoracic ganglia of the American cockroach Periplaneta americana L. Two types of tetrodotoxin-sensitive Na(+) currents were observed, with different voltage dependencies of channel inactivation. Type-I Na(+) currents were inactivated at more negative potentials than type-II Na(+) currents. As a result, these two types of Na(+) channels responded to indoxacarb compounds differentially. At a holding potential of -100 mV, type-I Na(+) currents were inhibited reversibly by 1 microM indoxacarb and irreversibly by 1 microM DCJW in a voltage-dependent manner, whereas type-II Na(+) currents were not affected by either of the compound. However, type-II Na(+) currents were inhibited by indoxacarb or DCJW at more depolarizing membrane potentials, ranging from -60 to -40 mV. The slow inactivation curves of type-I and type-II Na(+) channels were significantly shifted in the hyperpolarizing direction by indoxacarb and DCJW, suggesting that these compounds have high affinities for the inactivated state of the Na(+) channels. It was concluded that the differential blocking actions of indoxacarb insecticides on type-I and type-II Na(+) currents resulted from their different voltage dependence of Na(+) channel inactivation. The irreversible nature of DCJW block may be partially responsible for its potent action in insects.

摘要

茚虫威是一种新型杀虫剂,其脱甲氧羰基代谢物DCJW已知可阻断昆虫和哺乳动物的电压门控性钠通道,但阻断机制尚未完全明确。本研究旨在表征茚虫威和DCJW对蟑螂钠通道的作用。采用全细胞膜片钳技术,从美洲大蠊(Periplaneta americana L.)胸神经节急性分离的神经元中记录钠电流。观察到两种对河豚毒素敏感的钠电流,其通道失活的电压依赖性不同。I型钠电流在比II型钠电流更负的电位下失活。因此,这两种类型的钠通道对茚虫威化合物的反应不同。在-100 mV的钳制电位下,1 μM茚虫威可逆性抑制I型钠电流,1 μM DCJW以电压依赖性方式不可逆地抑制I型钠电流,而II型钠电流不受这两种化合物的影响。然而,在-60至-40 mV的更去极化膜电位下,II型钠电流受到茚虫威或DCJW的抑制。茚虫威和DCJW使I型和II型钠通道的慢失活曲线在超极化方向上显著移位,表明这些化合物对钠通道的失活状态具有高亲和力。得出的结论是,茚虫威杀虫剂对I型和II型钠电流的不同阻断作用是由于它们钠通道失活的电压依赖性不同。DCJW阻断的不可逆性质可能部分解释了其在昆虫中的强效作用。

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