Literature DB >> 3427273

Electrophysiological effects of labetalol on canine atrial, cardiac Purkinje fibres and ventricular muscle.

J G Mill1, F Riccioppo Neto.   

Abstract

1. Using conventional microelectrode techniques for the intracellular recordings of the membrane potential, the effects of labetalol were studied on cardiac Purkinje, atrial and ventricular muscle fibres of the dog. 2. Labetalol (1-10 microM) reduced, in a concentration-dependent manner, the action potential amplitude (APA) and the maximum rate of rise of the action potential (Vmax) in Purkinje fibres. 3. The action potential duration (APD) was decreased in Purkinje fibres but significantly increased in ventricular fibres after small concentrations of labetalol (1-3 microM). The atrial fibres were not very sensitive to labetalol. 4. Depolarization of the cardiac Purkinje fibres by increasing the external potassium concentration (8-12 mM), potentiated the labetalol effects on APA and Vmax but blocked its effects on the APD. 5. The effects of labetalol on Vmax of Purkinje fibres were dependent on the frequency of stimulation. 6. The ratio of the effective refractory period to the APD was increased both in normally polarized and depolarized Purkinje fibres after treatment with labetalol (10 microM). 7. Labetalol (10 microM) shifted the membrane responsiveness curve of Purkinje fibres by about 10 mV in the hyperpolarizing direction. 8. The slow response obtained in K-depolarized, Ba-treated Purkinje fibres was not significantly affected by labetalol (10-100 microM). 9. It is suggested that labetalol can exert Class I and Class III antiarrhythmic actions in cardiac muscle of the dog in vitro.

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Year:  1987        PMID: 3427273      PMCID: PMC1853676          DOI: 10.1111/j.1476-5381.1987.tb11365.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  25 in total

1.  The effect of the cardiac membrane potential on the rapid availability of the sodium-carrying system.

Authors:  S WEIDMANN
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2.  The differential effect of quinidine and pyrilamine on the myocardial action potential at various rates of stimulation.

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Journal:  J Pharmacol Exp Ther       Date:  1957-08       Impact factor: 4.030

Review 3.  Antiarrhythmic action of adrenergic beta-receptor blocking agents.

Authors:  S D Seth
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4.  Influences of labetalol a combined alpha- and beta-adrenergic blocking agent on the dysrhythmias induced by coronary occlusion and reperfusion.

Authors:  S M Pogwizd; A D Sharma; P B Corr
Journal:  Cardiovasc Res       Date:  1982-07       Impact factor: 10.787

Review 5.  A review of the animal pharmacology of labetalol, a combined alpha- and beta-adrenoceptor-blocking drug.

Authors:  R T Brittain; G P Levy
Journal:  Br J Clin Pharmacol       Date:  1976-08       Impact factor: 4.335

6.  Combined effects of rate membrane potential, and drugs on maximum rate of rise (Vmax) of action potential upstroke of guinea pig papillary muscle.

Authors:  C Chen; L S Gettes
Journal:  Circ Res       Date:  1976-06       Impact factor: 17.367

Review 7.  Current status of labetalol, the first alpha- and beta-blocking agent.

Authors:  J H Kanto
Journal:  Int J Clin Pharmacol Ther Toxicol       Date:  1985-11

8.  The role of catecholamines in the production of ischaemia-induced ventricular arrhythmias in the rat in vivo and in vitro.

Authors:  A Daugherty; K N Frayn; W S Redfern; B Woodward
Journal:  Br J Pharmacol       Date:  1986-01       Impact factor: 8.739

Review 9.  Ventricular antiarrhythmic effects of beta-adrenergic blocking drugs: a review of mechanism and clinical studies.

Authors:  C Pratt; E Lichstein
Journal:  J Clin Pharmacol       Date:  1982 Aug-Sep       Impact factor: 3.126

10.  Effects of cyproheptadine on electrophysiological properties of isolated cardiac muscle of dogs and rabbits.

Authors:  F Riccioppo Neto
Journal:  Br J Pharmacol       Date:  1983-10       Impact factor: 8.739

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  1 in total

1.  Antiarrhythmic efficacy of labetalol as assessed by programmed electrical stimulation.

Authors:  G Krumpl; H Todt; K Krejcy; G Raberger
Journal:  Br J Pharmacol       Date:  1990-08       Impact factor: 8.739

  1 in total

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