Arylnaphthalene lignans from Taiwania cryptomerioides as novel blockers of voltage-gated K+ channels

被引:8
作者
Leung, Yuk-Man [1 ]
Tsou, Yi-Huan [2 ]
Kuo, Chang-Shin [3 ]
Lin, Shang-Ying [2 ]
Wu, Pau-Yen [2 ]
Hour, Mann-Jen [2 ]
Kuo, Yueh-Hsiung [4 ]
机构
[1] China Med Univ, Grad Inst Neural & Cognit Sci, Taichung 40402, Taiwan
[2] China Med Univ, Dept Pharm, Taichung 40402, Taiwan
[3] China Med Univ, Dept Nutr, Taichung 40402, Taiwan
[4] China Med Univ, Tsuzuki Inst Tradit Med, Taichung 40402, Taiwan
关键词
Voltage-gated K+ channels; Arylnaphthalene lignans; Helioxanthin; Block; NORDIHYDROGUAIARETIC ACID; POTASSIUM CHANNELS; CELLS; APOPTOSIS; INACTIVATION; CURRENTS;
D O I
10.1016/j.phymed.2010.04.001
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Lignans are natural phytochemicals which exhibit multiple pharmacological effects such as anti-inflammation, antivirus and anti-tumor activities. Whether they have effects on neural tissues and ion channels is still unknown. The effects of several arylnaphathalene lignans purified from Taiwania cryptomerioides on voltage-gated K+ (Kv) channels in mouse neuroblastoma N2A cells were examined. These lignans included Taiwanin E. helioxanthin (HXT) and diphyllin. All lignans showed inhibitory effects on Kv channels and HXT was the most potent compound (IC50=1.7 mu M). The mechanism of HXT block was further investigated. Its action was found to be extracellular but not intracellular. HXT accelerated current decay, caused a left-shift in steady-state inactivation curve but had no effect on voltage-dependence of activation. HXT block was unaffected by intracellular K+ concentrations. Further, it did not affect ATP-sensitive K+ channels. Our data therefore suggest that HXT is a potent and specific blocker of Kv channels, possibly with an inhibitory mechanism involving acceleration of slow inactivation. (C) 2010 Elsevier GmbH. All rights reserved.
引用
收藏
页码:46 / 51
页数:6
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