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- Publisher Website: 10.1097/00005344-198407000-00001
- Scopus: eid_2-s2.0-0021141661
- PMID: 6206306
- WOS: WOS:A1984TB11800001
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Article: Electrophysiological effects of encainide (MJ9067) on canine subendocardial Purkinje fibers surviving infarction
Title | Electrophysiological effects of encainide (MJ9067) on canine subendocardial Purkinje fibers surviving infarction |
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Authors | |
Keywords | Canine Purkinje fibers surviving infarction Electrophysiology Encainide Stimulation frequency |
Issue Date | 1984 |
Publisher | Lippincott Williams & Wilkins. The Journal's web site is located at http://www.cardiovascularpharm.com/ |
Citation | Journal Of Cardiovascular Pharmacology, 1984, v. 6 n. 4, p. 547-554 How to Cite? |
Abstract | The electrophysiological effects of encainide (MJ9067) on canine subendocardial Purkinje fibers surviving infarction were examined 22-24 h after coronary artery ligation, using standard microelectrode techniques at pH 7.4. Encainide (5 and 10 μM) shortened APD50, decreased the action potential amplitude and overshoot, caused a 2-3 mV depolarization of the cell, and decreased the maximum rate of phase 0 depolarization. All these effects were dose dependent. APD90 was slightly, but not significantly, shortened. Encainide had a greater effect on APD50 than on APD90 at longer (1,000 ms) stimulation cycle lengths than at shorter (400 ms) cycle lengths. There was a significant interaction between the effects of stimulation rate and encainide concentration on APD90, APD50, amplitude, and overshoot. The same parameters measured at a lower pH (7.1) gave similar results. There was a significant correlation (r = -0.540, p < 0.001) between the control APD90 and the degree and direction of change of APD90 after 10 μM encainide. Automaticity of the infarcted preparations was eliminated or slowed in a dose-dependent fashion by 5 and 10 μM encainide. The curve relating membrane potential and the maximum rate of phase 0 depolarization was shifted down and toward higher potentials by 5 μM encainide. The results show that encainide produces similar changes in the action potentials of Purkinje fibers surviving infarction as in normal Purkinje fibers, and is effective in lowering the rate of spontaneous depolarizations in infarcted tissue. Furthermore, encainide appears to be the only antiarrhythmic drug which has been shown to increase and decrease APD90, depending on the initial APD90 of the cell. |
Persistent Identifier | http://hdl.handle.net/10722/170721 |
ISSN | 2023 Impact Factor: 2.6 2023 SCImago Journal Rankings: 0.610 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | King, BW | en_US |
dc.contributor.author | Man, RYK | en_US |
dc.date.accessioned | 2012-10-30T06:10:35Z | - |
dc.date.available | 2012-10-30T06:10:35Z | - |
dc.date.issued | 1984 | en_US |
dc.identifier.citation | Journal Of Cardiovascular Pharmacology, 1984, v. 6 n. 4, p. 547-554 | en_US |
dc.identifier.issn | 0160-2446 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/170721 | - |
dc.description.abstract | The electrophysiological effects of encainide (MJ9067) on canine subendocardial Purkinje fibers surviving infarction were examined 22-24 h after coronary artery ligation, using standard microelectrode techniques at pH 7.4. Encainide (5 and 10 μM) shortened APD50, decreased the action potential amplitude and overshoot, caused a 2-3 mV depolarization of the cell, and decreased the maximum rate of phase 0 depolarization. All these effects were dose dependent. APD90 was slightly, but not significantly, shortened. Encainide had a greater effect on APD50 than on APD90 at longer (1,000 ms) stimulation cycle lengths than at shorter (400 ms) cycle lengths. There was a significant interaction between the effects of stimulation rate and encainide concentration on APD90, APD50, amplitude, and overshoot. The same parameters measured at a lower pH (7.1) gave similar results. There was a significant correlation (r = -0.540, p < 0.001) between the control APD90 and the degree and direction of change of APD90 after 10 μM encainide. Automaticity of the infarcted preparations was eliminated or slowed in a dose-dependent fashion by 5 and 10 μM encainide. The curve relating membrane potential and the maximum rate of phase 0 depolarization was shifted down and toward higher potentials by 5 μM encainide. The results show that encainide produces similar changes in the action potentials of Purkinje fibers surviving infarction as in normal Purkinje fibers, and is effective in lowering the rate of spontaneous depolarizations in infarcted tissue. Furthermore, encainide appears to be the only antiarrhythmic drug which has been shown to increase and decrease APD90, depending on the initial APD90 of the cell. | en_US |
dc.language | eng | en_US |
dc.publisher | Lippincott Williams & Wilkins. The Journal's web site is located at http://www.cardiovascularpharm.com/ | en_US |
dc.relation.ispartof | Journal of Cardiovascular Pharmacology | en_US |
dc.subject | Canine Purkinje fibers surviving infarction | - |
dc.subject | Electrophysiology | - |
dc.subject | Encainide | - |
dc.subject | Stimulation frequency | - |
dc.subject.mesh | Action Potentials - Drug Effects | en_US |
dc.subject.mesh | Anilides - Pharmacology | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Anti-Arrhythmia Agents - Pharmacology | en_US |
dc.subject.mesh | Dogs | en_US |
dc.subject.mesh | Electric Stimulation | en_US |
dc.subject.mesh | Electrophysiology | en_US |
dc.subject.mesh | Encainide | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Heart Conduction System - Drug Effects | en_US |
dc.subject.mesh | Hydrogen-Ion Concentration | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Membrane Potentials - Drug Effects | en_US |
dc.subject.mesh | Myocardial Infarction - Physiopathology | en_US |
dc.subject.mesh | Purkinje Fibers - Drug Effects | en_US |
dc.title | Electrophysiological effects of encainide (MJ9067) on canine subendocardial Purkinje fibers surviving infarction | en_US |
dc.type | Article | en_US |
dc.identifier.email | Man, RYK:rykman@hkucc.hku.hk | en_US |
dc.identifier.authority | Man, RYK=rp00236 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1097/00005344-198407000-00001 | - |
dc.identifier.pmid | 6206306 | - |
dc.identifier.scopus | eid_2-s2.0-0021141661 | en_US |
dc.identifier.volume | 6 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 547 | en_US |
dc.identifier.epage | 554 | en_US |
dc.identifier.isi | WOS:A1984TB11800001 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | King, BW=7402688421 | en_US |
dc.identifier.scopusauthorid | Man, RYK=7004986435 | en_US |
dc.identifier.issnl | 0160-2446 | - |