Modulation of tetrodotoxin-resistant sodium channels by dihydropyrazole insecticide RH-3421 in rat dorsal root ganglion neurons

被引:15
|
作者
Tsurubuchi, Y
Zhao, XL
Nagata, K
Kono, Y
Nishimura, K
Yeh, JZ
Narahashi, T
机构
[1] Northwestern Univ, Sch Med, Dept Mol Pharmacol & Biol Chem, Chicago, IL 60611 USA
[2] Univ Tsukuba, Inst Agr & Forestry, Tsukuba, Ibaraki 3058572, Japan
[3] RIKEN, Inst Phys & Chem Res, Brain Sci Inst, Wako, Saitama 3510198, Japan
[4] Univ Osaka Prefecture, Res Inst Adv Sci & Technol, Sakai, Osaka 5998570, Japan
关键词
sodium channel; dihydropyrazole; RH-3421; tetrodotoxin-resistant sodium channel; dorsal root ganglion;
D O I
10.1016/S0161-813X(01)00058-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of the dihydropyrazole insecticide RH-3421 on the tetrodotoxin-resistant (M-R) voltage-gated sodium channels in rat dorsal root ganglion (DRG) neurons were studied using the whole-cell patch clamp technique. RH-3421 at 10 nM to 1 muM completely blocked action potentials. The sodium currents were irreversibly suppressed by 1 muM RH-3421 in a time- and a dose-dependent manner and the IC50 value of RH-3421 was estimated to be 0.7 muM after 10 min of application. RH-3421 blocked the sodium currents to the same extent over the entire range of test potentials. The sodium conductance-voltage curve was not shifted along the voltage axis by 1 muM RH-3421 application. In contrast, both fast and slow steady-state sodium channel inactivation curves were shifted in the hyperpolarizing direction in the presence of 1 muM RH-3421. It was concluded that RH-3421 bound to the resting and inactivated sodium channels to cause block with a higher affinity for the latter state. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
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页码:743 / 753
页数:11
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