Search Results - "Sunami, Akihiko"

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  1. 1

    Mexiletine Block of Voltage-Gated Sodium Channels: Isoform- and State-Dependent Drug-Pore Interactions by Nakagawa, Hiroki, Munakata, Tatsuo, Sunami, Akihiko

    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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    Journal Article
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    Electrophysiological effects of ginseng and ginsenoside Re in guinea pig ventricular myocytes by Bai, Chang-Xi, Sunami, Akihiko, Namiki, Takao, Sawanobori, Tohru, Furukawa, Tetsushi

    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 by Sunami, Akihiko, Tracey, Arlene, Glaaser, Ian W., Lipkind, Gregory M., Hanck, Dorothy A., Fozzard, Harry A.

    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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    Journal Article
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    Sodium Channel Selectivity Filter Regulates Antiarrhythmic Drug Binding by Sunami, Akihiko, Dudley, Samuel C., Fozzard, Harry A.

    “…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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    Journal Article
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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 by Sunami, Akihiko, Glaaser, Ian W., Fozzard, Harry A.

    “…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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    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 by Sunami, A, Glaaser, I W, Fozzard, H A

    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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    Journal Article
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    A Genetically Encoded Bioluminescent Indicator for the Sodium Channel Activity in Living Cells by Kaihara, Asami, Sunami, Akihiko, Kurokawa, Junko, Furukawa, Tetsushi

    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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    New observations on the mechanisms of antiarrhythmic actions of disopyramide on cardiac membranes by Hiraoka, Masayasu, Kuga, Keisuke, Kawano, Seiko, Sunami, Akihiko, Fan, Zhen

    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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    Journal Article Conference Proceeding
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    Electrophysiological properties of a new antiarrhythmic agent, bisaramil on guinea-pig, rabbit and canine cardiac preparations by Sunami, A, Sawanobori, T, Adaniya, H, Hiraoka, M

    “…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 by YAMAWAKI, Ichiro, BUKOVAC, Scott W., SUNAMI, Akihiko

    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 by Sunami, Akihiko, Tracey, Arlene, Glaaser, Ian W, Lipkind, Gregory M, Hanck, Dorothy A, Fozzard, Harry A

    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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    Journal Article
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    Involvement of local anesthetic binding sites on IVS6 of sodium channels in fast and slow inactivation by Bai, Chang-Xi, Glaaser, Ian W., Sawanobori, Tohru, Sunami, Akihiko

    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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    Journal Article
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    Cardiac-Specific External Paths for Lidocaine, Defined by Isoform-Specific Residues, Accelerate Recovery From Use-Dependent Block by Lee, Peter J, Sunami, Akihiko, Fozzard, Harry A

    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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    Journal Article
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    Pharmacological studies on proglumetacin maleate, a new non-steroidal anti-inflammatory drug. (2). Analgesic and antipyretic effects by Ono, N, Sunami, A, Yamamoto, N, Yamasaki, Y, Miyake, H

    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 by Ono, N, Yamamoto, N, Sunami, A, Yamasaki, Y, Miyake, H

    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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