La maladie de Parkinson en France (serveur d'exploration)

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Electrophysiological action of bepridil on atrioventricular accessory pathways.

Identifieur interne : 001C45 ( Ncbi/Merge ); précédent : 001C44; suivant : 001C46

Electrophysiological action of bepridil on atrioventricular accessory pathways.

Auteurs : P. Touboul [France] ; G. Atallah ; G. Kirkorian ; P. Lavaud ; J R Kieny ; M P Mathieu ; A. Dellinger

Source :

RBID : pubmed:3499924

English descriptors

Abstract

The electrophysiologic properties of bepridil, a calcium channel blocker with additional effects on fast response tissues, were investigated in 10 patients with atrioventricular accessory pathways. Seven patients had Wolff-Parkinson-White syndrome, and three had concealed atrioventricular pre-excitation. A dose of 4 mg/kg was administered intravenously over five minutes. Bepridil increased the AH interval and the functional refractory period of the atrioventricular node. The effective refractory periods of the right atrium and right ventricle were also increased. Bepridil prolonged refractoriness in the accessory pathway both in the anterograde and retrograde direction. After bepridil administration it was impossible to induce reciprocating tachycardia electrically in two patients because of conduction block in the normal pathway. On the other hand, the zone of tachycardia was often increased after bepridil. Nevertheless, the heart rate during tachycardia was slowed by depression of conduction in both the normal and accessory pathways. The findings of this study provide a basis for the antiarrhythmic action of bepridil in patients with atrioventricular accessory pathways.

PubMed: 3499924

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pubmed:3499924

Le document en format XML

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<div type="abstract" xml:lang="en">The electrophysiologic properties of bepridil, a calcium channel blocker with additional effects on fast response tissues, were investigated in 10 patients with atrioventricular accessory pathways. Seven patients had Wolff-Parkinson-White syndrome, and three had concealed atrioventricular pre-excitation. A dose of 4 mg/kg was administered intravenously over five minutes. Bepridil increased the AH interval and the functional refractory period of the atrioventricular node. The effective refractory periods of the right atrium and right ventricle were also increased. Bepridil prolonged refractoriness in the accessory pathway both in the anterograde and retrograde direction. After bepridil administration it was impossible to induce reciprocating tachycardia electrically in two patients because of conduction block in the normal pathway. On the other hand, the zone of tachycardia was often increased after bepridil. Nevertheless, the heart rate during tachycardia was slowed by depression of conduction in both the normal and accessory pathways. The findings of this study provide a basis for the antiarrhythmic action of bepridil in patients with atrioventricular accessory pathways.</div>
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<RefSource>Am J Cardiol. 1987 Jan 1;59(1):89-92</RefSource>
<PMID Version="1">3492906</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>Circ Res. 1970 Sep;27(3):345-59</RefSource>
<PMID Version="1">5452734</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>Circulation. 1975 Oct;52(4):552-62</RefSource>
<PMID Version="1">1157268</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>Am J Cardiol. 1977 Oct;40(4):514-20</RefSource>
<PMID Version="1">910715</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>Prog Cardiovasc Dis. 1978 Jan-Feb;20(4):285-327</RefSource>
<PMID Version="1">146210</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>J Pharmacol Exp Ther. 1979 Sep;210(3):378-85</RefSource>
<PMID Version="1">480188</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>Therapie. 1980 Sep-Oct;35(5):607-12</RefSource>
<PMID Version="1">6970998</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Cardiovasc Pharmacol. 1981 Jul-Aug;3(4):655-67</RefSource>
<PMID Version="1">6167797</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Circulation. 1982 Feb;65(2):348-54</RefSource>
<PMID Version="1">7053894</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Ann Cardiol Angeiol (Paris). 1982 Jul-Sep;31(5):409-15</RefSource>
<PMID Version="1">6984315</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Arch Mal Coeur Vaiss. 1983 Mar;76(3):341-8</RefSource>
<PMID Version="1">6409035</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Cardiol. 1984 Sep 1;54(6):579-81</RefSource>
<PMID Version="1">6332516</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Am J Cardiol. 1985 Jun 1;55(13 Pt 1):1513-9</RefSource>
<PMID Version="1">3873867</PMID>
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<CommentsCorrections RefType="Cites">
<RefSource>Am J Cardiol. 1985 Jun 1;55(13 Pt 1):1589-95</RefSource>
<PMID Version="1">3873868</PMID>
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<RefSource>Arch Mal Coeur Vaiss. 1985 Apr;78(4):612-9</RefSource>
<PMID Version="1">3923987</PMID>
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