Search Results - "Sunami, Akihiko"
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Mexiletine Block of Voltage-Gated Sodium Channels: Isoform- and State-Dependent Drug-Pore Interactions
Published in Molecular pharmacology (01-03-2019)“…Mexiletine is a class Ib antiarrhythmic drug and is also used clinically to reduce or prevent myotonia. In addition, mexiletine has neuroprotective effects in…”
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Drug-Binding Sites of Cardiac Sodium Channel
Published in Journal of arrhythmia (2011)Get full text
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Electrophysiological effects of ginseng and ginsenoside Re in guinea pig ventricular myocytes
Published in European journal of pharmacology (22-08-2003)“…Panax ginseng is a folk medicine with various cardiovascular actions; however, its underlying mechanisms of action are not well known. In the present study, we…”
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Accessibility of mid-segment domain IV S6 residues of the voltage-gated Na+ channel to methanethiosulfonate reagents
Published in The Journal of physiology (01-12-2004)“…The inner pore of the voltage-gated Na + channel is predicted by the structure of bacterial potassium channels to be lined with the four S6 α-helical…”
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5
Sodium Channel Selectivity Filter Regulates Antiarrhythmic Drug Binding
Published in Proceedings of the National Academy of Sciences - PNAS (09-12-1997)“…Local anesthetic antiarrhythmic drugs block Na+channels and have important clinical uses. However, the molecular mechanism by which these drugs block the…”
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A Critical Residue for Isoform Difference in Tetrodotoxin Affinity Is a Molecular Determinant of the External Access Path for Local Anesthetics in the Cardiac Sodium Channel
Published in Proceedings of the National Academy of Sciences - PNAS (29-02-2000)“…Membrane-impermeant quaternary derivatives of lidocaine (QX222 and QX314) block cardiac Na+channels when applied from either side of the membrane, but they…”
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Unexpected mexiletine responses of a mutant cardiac Na+ channel implicate the selectivity filter as a structural determinant of antiarrhythmic drug access
Published in Molecular pharmacology (01-08-2004)“…Gating properties of Na(+) channels are the critical determinants for the state-dependent block by class I antiarrhythmic drugs; however, recent site-directed…”
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Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics
Published in Molecular pharmacology (01-04-2001)“…Membrane-impermeant quaternary amine local anesthetics QX314 and QX222 can access their binding site on the cytoplasmic side of the selectivity filter from the…”
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The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
Published in The Journal of clinical investigation (01-06-2008)“…Phenotypic overlap of type 3 long QT syndrome (LQT3) with Brugada syndrome (BrS) is observed in some carriers of mutations in the Na channel SCN5A. While this…”
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A Genetically Encoded Bioluminescent Indicator for the Sodium Channel Activity in Living Cells
Published in Journal of the American Chemical Society (01-04-2009)“…We have developed a genetically encoded bioluminescent indicator for the Na+ channel, in which Na+-sensitive Gaussia luciferase is fused with the voltage-gated…”
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Role of L1462 in Nav1.5 Channel DIII-S6 in Voltage-dependent Gating and Antiarrhythmic Block
Published in Biophysical journal (01-02-2009)Get full text
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New observations on the mechanisms of antiarrhythmic actions of disopyramide on cardiac membranes
Published in The American journal of cardiology (05-12-1989)“…Electrophysiologic effects of disopyramide on cardiac membranes were studied using the microelectrode technique applied to papillary muscles and the suction…”
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Electrophysiological properties of a new antiarrhythmic agent, bisaramil on guinea-pig, rabbit and canine cardiac preparations
Published in Naunyn-Schmiedeberg's archives of pharmacology (01-09-1991)“…Electrophysiological effects of bisaramil, a novel antiarrhythmic agent, were examined using the conventional microelectrode technique applied to cardiac…”
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Synthesis and Biological Activity of the Metabolites of syn-3-Ethyl-7-methyl-3, 7-diazabicyclo[3.3.1]non-9-yl 4-Chlorobenzoate Hydrochloride
Published in Chemical & pharmaceutical bulletin (01-11-1994)“…Five metabolites of syn-3-ethyl-7-methyl-3, 7-diazabicyclo[3.3.1]non-9-yl 4-chlorobenzoate hydrochloride (YUTAC)(1) were prepared and examined for Na+ current…”
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Accessibility of mid-segment domain IV S6 residues of the voltage-gated Na super(+) channel to methanethiosulfonate reagents
Published in The Journal of physiology (01-12-2004)“…The inner pore of the voltage-gated Na super(+) channel is predicted by the structure of bacterial potassium channels to be lined with the four S6 alpha-…”
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Involvement of local anesthetic binding sites on IVS6 of sodium channels in fast and slow inactivation
Published in Neuroscience letters (30-01-2003)“…Local anesthetics (LAs) block Na + channels with a higher affinity for the fast or slow inactivated state of the channel. Their binding to the channel may…”
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Cardiac-Specific External Paths for Lidocaine, Defined by Isoform-Specific Residues, Accelerate Recovery From Use-Dependent Block
Published in Circulation research (23-11-2001)“…Local anesthetic antiarrhythmic drugs block voltage-gated Na channels from the cytoplasmic side. In addition, cardiac Na channels can be also blocked by the…”
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Pharmacological studies on proglumetacin maleate, a new non-steroidal anti-inflammatory drug. (2). Analgesic and antipyretic effects
Published in Nihon yakurigaku zasshi (01-08-1986)“…Analgesic and antipyretic effects of proglumetacin maleate (PGM), a new indomethacin (IND) derivative, were investigated in comparison with those of IND on an…”
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Pharmacological studies on proglumetacin maleate, a new non-steroidal anti-inflammatory drug. (1). Anti-inflammatory effects
Published in Nihon yakurigaku zasshi (01-07-1986)“…Anti-inflammatory effects of proglumetacin maleate (PGM), a new indomethacin (IND) derivative, were compared with those of IND on an equimolar-dose basis. PGM…”
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