Literature DB >> 7186821

Antiarrhythmic effects of Org 6001 in rats: correlation with plasma and tissue drug concentrations.

K Kane, F McDonald, J Parratt, C Timmer, J Vink.   

Abstract

The antiarrhythmic effects of Org 6001 following oral administration in the rat have been assessed and correlated with plasma, myocardial and skeletal muscle drug concentrations. Arrythmias were induced by coronary artery ligation in anaesthetized rats. Org 6001 (10, 20, 50 and 100 mg/kg given 1 h before ligation) significantly reduced mortality and the incidence of ventricular fibrillation in the 0-30 min post ligation period. Only the highest dose of drug also significantly reduced the number of ventricular ectopic beats following ligation. A linear relationship was observed between the oral dose and the Org 6001 concentrations in plasma and skeletal muscle determined 90 min after drug administration. The Org 6001 concentration in the myocardium was not linearly related to the administered dose and Org 6001 appeared to be concentrated to a higher extent in cardiac than in skeletal muscle at that time. No statistically significant difference in drug levels in the ischaemic left ventricle and normal right ventricle plus septum was observed. The antiarrythmic effect of Org 6001, as measured by changes in the incidence of ventricular fibrillation, correlated with myocardial concentrations of the drug.

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Year:  1982        PMID: 7186821      PMCID: PMC2071599          DOI: 10.1111/j.1476-5381.1982.tb08789.x

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


  13 in total

1.  The physiological disposition and cardiac effects of procaine amide.

Authors:  L C MARK; H J KAYDEN; J M STEELE; J R COOPER; I BERLIN; E A ROVENSTINE; B B BRODIE
Journal:  J Pharmacol Exp Ther       Date:  1951-05       Impact factor: 4.030

2.  The effects of prolonged oral administration of a new antidysrhythmic drug (Org 6001) on coronary artery ligation dysrhythmias in conscious and anesthetized rats.

Authors:  K A Kane; I Leprán; F M McDonald; J R Parratt; L Szekeres
Journal:  J Cardiovasc Pharmacol       Date:  1980 Jul-Aug       Impact factor: 3.105

3.  Strain differences in rat adrenal biosynthetic enzymes and stress-induced increases in plasma catecholamines.

Authors:  R McCarty; G M Gilad; V K Weise; I J Kopin
Journal:  Life Sci       Date:  1979-08-27       Impact factor: 5.037

4.  Disopyramide plasma and myocardial tissue concentrations as they relate to antiarrhythmic activity.

Authors:  E Patterson; P Stetson; B R Lucchesi
Journal:  J Cardiovasc Pharmacol       Date:  1979 Sep-Oct       Impact factor: 3.105

5.  Tissue distribution and elimination of digoxin and methyldigoxin after single and multiple doses in dogs.

Authors:  J Kuhlmann; N Rietbrock; B Schnieders
Journal:  J Cardiovasc Pharmacol       Date:  1979 Mar-Apr       Impact factor: 3.105

6.  Disopyramide phosphate: tissue uptake and relationship between drug concentrations in the plasma and myocardium of rats.

Authors:  A Karim; C Kook; J Campion; M Doherty
Journal:  Arch Int Pharmacodyn Ther       Date:  1977-08

7.  Correlation of the electrophysiological and antiarrhythmic properties of the N-acetyl metabolite of procainamide with plasma and tissue drug concentrations in the dog.

Authors:  E E Bagwell; T Walle; D E Drayer; M M Reidenbert; J K Pruett
Journal:  J Pharmacol Exp Ther       Date:  1976-04       Impact factor: 4.030

8.  A comparison of the accumulation and release of 3H-ouabain and 3H-digitoxin by guinea-pig heart muscle.

Authors:  K Kuschinsky; H Lüllmann; P A van Zwieten
Journal:  Br J Pharmacol Chemother       Date:  1968-03

9.  Coronary artery ligation in anesthetized rats as a method for the production of experimental dysrhythmias and for the determination of infarct size.

Authors:  C Clark; M I Foreman; K A Kane; F M McDonald; J R Parratt
Journal:  J Pharmacol Methods       Date:  1980-06

10.  Determination of nanogram amounts of the antiarrhythmic drug Org 6001 in biological fluids and tissues using selected ion monitoring.

Authors:  J Vink; H J van Hal; C J Timmer
Journal:  Biomed Mass Spectrom       Date:  1980-11
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