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Potassium channel blockers and neuronal function.

作者信息

Harvey A L, Rowan E G, Anderson A J

机构信息

Department of Physiology and Pharmacology, University of Strathclyde, Great Britain.

出版信息

Pflugers Arch. 1989;414 Suppl 1:S106-10. doi: 10.1007/BF00582257.

DOI:10.1007/BF00582257
PMID:2674890
Abstract
摘要

相似文献

1
Potassium channel blockers and neuronal function.钾通道阻滞剂与神经元功能。
Pflugers Arch. 1989;414 Suppl 1:S106-10. doi: 10.1007/BF00582257.
2
[Effect of vinpocetine on various high threshold potassium currents in the mollusk neurons].
Biull Eksp Biol Med. 1998 Oct;126(10):408-11.
3
Voltage-gated K+ channel modulators as neuroprotective agents.电压门控钾通道调节剂作为神经保护剂。
Life Sci. 2010 May 22;86(21-22):775-80. doi: 10.1016/j.lfs.2010.04.004. Epub 2010 Apr 10.
4
[A single calcium channel with anomalous rectification in mollusk neurons].[软体动物神经元中具有异常整流的单个钙通道]
Neirofiziologiia. 1989;21(1):31-8.
5
Role of potassium channels in Abeta(1-40)-activated apoptotic pathway in cultured cortical neurons.钾通道在培养的皮质神经元中β-淀粉样蛋白(1-40)激活的凋亡途径中的作用。
J Neurosci Res. 2006 Nov 15;84(7):1475-84. doi: 10.1002/jnr.21054.
6
[Effect of chlorofos on high-threshold potassium and calcium channels in the neuronal membrane].[毒死蜱对神经元膜上高阈值钾通道和钙通道的影响]
Biull Eksp Biol Med. 1996 Jan;121(1):59-62.
7
Effects of various K+ channel blockers on spontaneous glycine release at rat spinal neurons.各种钾离子通道阻滞剂对大鼠脊髓神经元甘氨酸自发释放的影响。
Brain Res. 2007 Jul 9;1157:11-22. doi: 10.1016/j.brainres.2006.09.097. Epub 2007 Jun 6.
8
Volatile general anesthetics produce hyperpolarization of Aplysia neurons by activation of a discrete population of baseline potassium channels.挥发性全身麻醉药通过激活离散的基线钾通道群使海兔神经元超极化。
Anesthesiology. 1996 Oct;85(4):889-900. doi: 10.1097/00000542-199610000-00026.
9
Discovering potassium channel blockers from synthetic compound database by using structure-based virtual screening in conjunction with electrophysiological assay.通过结合基于结构的虚拟筛选和电生理测定从合成化合物数据库中发现钾通道阻滞剂。
J Med Chem. 2007 Jan 11;50(1):83-93. doi: 10.1021/jm060414o.
10
[Inhibition of salicylate on potassium channels in rat inferior colliculus neurons].[水杨酸盐对大鼠下丘神经元钾通道的抑制作用]
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2005 Nov;40(11):835-9.

本文引用的文献

1
Dendrotoxin from the venom of the green mamba, Dendroaspis angusticeps. A neurotoxin that enhances acetylcholine release at neuromuscular junction.绿曼巴蛇(Dendroaspis angusticeps)毒液中的树突毒素。一种神经毒素,可增强神经肌肉接头处乙酰胆碱的释放。
Naunyn Schmiedebergs Arch Pharmacol. 1980 May;312(1):1-6. doi: 10.1007/BF00502565.
2
Protease inhibitor homologues from mamba venoms: facilitation of acetylcholine release and interactions with prejunctional blocking toxins.来自曼巴蛇毒液的蛋白酶抑制剂同源物:促进乙酰胆碱释放及与接头前阻断毒素的相互作用
Br J Pharmacol. 1982 Sep;77(1):153-61. doi: 10.1111/j.1476-5381.1982.tb09281.x.
3
Potassium currents in the frog node of Ranvier.
蛙类郎飞结中的钾电流。
Prog Biophys Mol Biol. 1983;42(1):1-20. doi: 10.1016/0079-6107(83)90002-0.
4
Presynaptic currents in mouse motor endings.小鼠运动终末的突触前电流。
J Physiol. 1982 Dec;333:619-36. doi: 10.1113/jphysiol.1982.sp014472.
5
Capsaicin blocks one class of K+ channels in the frog node of Ranvier.辣椒素可阻断青蛙郎飞结处的一类钾离子通道。
Brain Res. 1982 Aug 12;245(2):372-5. doi: 10.1016/0006-8993(82)90820-4.
6
[Modifications by 4 amino-pyridine of electric characteristics of the isolated giant axon of an insect, the cockroach (Periplaneta americana L.)].
C R Seances Soc Biol Fil. 1974;168(1):27-34.
7
Excitatory actions of tetrahydro-9-aminoacridine (THA) on hippocampal pyramidal neurons.四氢-9-氨基吖啶(THA)对海马锥体神经元的兴奋作用。
Neurosci Lett. 1987 Aug 31;79(3):301-5. doi: 10.1016/0304-3940(87)90448-4.
8
Potassium channel blocking actions of beta-bungarotoxin and related toxins on mouse and frog motor nerve terminals.β-银环蛇毒素及相关毒素对小鼠和青蛙运动神经末梢的钾通道阻断作用。
Br J Pharmacol. 1988 Jul;94(3):839-47. doi: 10.1111/j.1476-5381.1988.tb11595.x.
9
Dendrotoxin-sensitive K+ channels in dorsal root ganglion cells.背根神经节细胞中的树突毒素敏感钾通道。
Neurosci Lett. 1988 Oct 31;93(1):49-55. doi: 10.1016/0304-3940(88)90011-0.
10
Effects of the facilitatory compounds catechol, guanidine, noradrenaline and phencyclidine on presynaptic currents of mouse motor nerve terminals.易化性化合物儿茶酚、胍、去甲肾上腺素和苯环利定对小鼠运动神经末梢突触前电流的影响。
Naunyn Schmiedebergs Arch Pharmacol. 1988 Aug;338(2):133-7. doi: 10.1007/BF00174860.