Search Results - "Delpón, E"
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1
Effects of atorvastatin and simvastatin on atrial plateau currents
Published in Journal of molecular and cellular cardiology (01-05-2007)“…Abstract Recent evidence has shown that the inhibitors of the 3-hydroxy-3-methylglutaryl coenzyme A reductase (statins) might exert antiarrhythmic effects both…”
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2
Stereoselective block of a human cardiac potassium channel (Kv1.5) by bupivacaine enantiomers
Published in Biophysical journal (01-08-1995)“…Stereoselective drug-channel interactions may help to elucidate the molecular basis of voltage-gated potassium channel block by local anesthetic drugs. We…”
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3
Regulation of cardiac ion channels by transcription factors: Looking for new opportunities of druggable targets for the treatment of arrhythmias
Published in Biochemical pharmacology (01-10-2022)“…[Display omitted] Cardiac electrical activity is governed by different ion channels that generate action potentials. Acquired or inherited abnormalities in the…”
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4
Losartan and its metabolite E3174 modify cardiac delayed rectifier K+ currents
Published in Circulation (New York, N.Y.) (14-03-2000)“…The effects of type 1 angiotensin II receptor antagonist losartan and its metabolite E3174 on transmembrane action potentials, hKv1.5, HERG, and I(Ks) currents…”
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5
Pharmacology of cardiac potassium channels
Published in Cardiovascular research (01-04-2004)“…Cardiac K+ channels are membrane-spanning proteins that allow the passive movement of K+ ions across the cell membrane along its electrochemical gradient. They…”
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6
Direct effects of candesartan and eprosartan on human cloned potassium channels involved in cardiac repolarization
Published in Molecular pharmacology (01-04-2001)“…In the present study, we analyzed the effects of two angiotensin II type 1 receptor antagonists, candesartan (0.1 microM) and eprosartan (1 microM), on hKv1.5,…”
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7
New investigational drugs for the management of acute heart failure syndromes
Published in Current medicinal chemistry (01-02-2010)“…Acute heart failure syndromes (AHFS) enclose a broad spectrum of conditions with different clinical presentations, heart failure history, pathophysiology,…”
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8
Bupivacaine effects on hKv1.5 channels are dependent on extracellular pH
Published in British journal of pharmacology (01-09-2001)“…Bupivacaine‐induced cardiotoxicity increases in hypoxic and acidotic conditions. We have analysed the effects of R(+)bupivacaine on hKv1.5 channels stably…”
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9
Effects of bupivacaine and a novel local anesthetic, IQB-9302, on human cardiac K+ channels
Published in The Journal of pharmacology and experimental therapeutics (01-02-2001)“…We have studied and compared the effects of bupivacaine with those induced by a new local anesthetic, IQB-9302, on human cardiac K+ channels hKv1.5, Kv2.1,…”
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10
Stereoselective effects of the enantiomers of a new local anaesthetic, IQB‐9302, on a human cardiac potassium channel (Kv1.5)
Published in British journal of pharmacology (01-01-2001)“…The N‐substituent of IQB‐9302 has the same number of carbons as bupivacaine, but it exhibits a different spatial localization (n‐butyl vs cyclopropylmethyl)…”
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11
Effects of propafenone and 5‐hydroxy‐propafenone on hKv1.5 channels
Published in British journal of pharmacology (01-11-1998)“…1 The goal of this study was to analyse the effects of propafenone and its major metabolite, 5‐hydroxy‐propafenone, on a human cardiac K+ channel (hKv1.5)…”
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12
Molecular Determinants of Stereoselective Bupivacaine Block of hKv1.5 Channels
Published in Circulation research (01-12-1997)“…Enantiomers of local anesthetics are useful probes of ion channel structure that can reveal three-dimensional relations for drug binding in the channel pore…”
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13
Effects of rupatadine, a new dual antagonist of histamine and platelet‐activating factor receptors, on human cardiac Kv1.5 channels
Published in British journal of pharmacology (01-11-1999)“…The effects of rupatadine, a new dual antagonist of both histamine H1 and platelet‐activating factor receptors, were studied on human cloned hKv1.5 channels…”
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14
Block of human cardiac Kv1.5 channels by loratadine : voltage-, time-and use-dependent block at concentrations above therapeutic levels
Published in Cardiovascular research (01-08-1997)“…The aim of this study was to analyze the effects of loratadine on a human cardiac K+ channel (hKv1.5) cloned from human ventricle and stably expressed in a…”
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15
Effects of a quaternary bupivacaine derivative on delayed rectifier K+ currents
Published in British journal of pharmacology (01-05-2000)“…Block of hKv1.5 channels by R‐bupivacaine has been attributed to the interaction of the charged form of the drug with an intracellular receptor. However,…”
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16
Structural determinants of potency and stereoselective block of hKv1.5 channels induced by local anesthetics
Published in Molecular pharmacology (01-07-1998)“…Block of hKv1.5 channels by bupivacaine is stereoselective, with (R)-(+)-bupivacaine being 7-fold more potent than (S)-(-)-bupivacaine. The study of the…”
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17
Blockade of cardiac potassium and other channels by antihistamines
Published in Drug safety (1999)“…The use of terfenadine and astemizole, two long-acting nonsedating histamine H1 receptor antagonists, has been associated with prolongation of the QT interval,…”
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18
Benzocaine enhances and inhibits the K+ current through a human cardiac cloned channel (Kv1.5)
Published in Cardiovascular research (01-05-1999)“…The aim of this study was to analyze the effects of a neutral local anaesthetic, benzocaine, on a cardiac K+ channel cloned from human ventricle. Experiments…”
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19
Imipramine Blocks Rapidly Activating and Delays Slowly Activating K+ Current Activation in Guinea Pig Ventricular Myocytes
Published in Circulation research (01-04-1994)“…Imipramine is a tricyclic antidepressant drug that also exhibits antiarrhythmic effects and whose clinical spectrum of activity is similar to that of…”
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20
Mechanisms of block of a human cloned potassium channel by the enantiomers of a new bradycardic agent: S‐16257‐2 and S‐16260‐2
Published in British journal of pharmacology (01-03-1996)“…1 The effects of S‐16257‐2 (S57) and S‐16260‐2 (R60), the two enantiomers of a new bradycardic agent, were studied on human cloned K+ channels (hKv1.5) stably…”
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