Literature DB >> 8097953

Effect of flosequinan on ischaemia-induced arrhythmias and on ventricular cyclic nucleotide content in the anaesthetized rat.

R B Jones1, G Frodsham, K Dickinson, G A Foster.   

Abstract

1. Flosequinan, milrinone, isoprenaline and forskolin given intravenously at similarly hypotensive doses have been evaluated in separate studies for their effect on ischaemia-induced arrhythmias and on ventricular cyclic nucleotide content following coronary artery ligation in the pentobarbitone anaesthetized rat. 2. Flosequinan did not affect mortality or arrhythmias following coronary artery ligation in either study and no change in ventricular cyclic nucleotide content was observed. 3. Isoprenaline caused a significant increase in mortality (P < 0.05) in both studies whereas milrinone and forskolin caused a significant increase in mortality in only one of the two studies conducted. All three agents caused significant increases in cyclic AMP which were associated with increased incidence of arrhythmias. 4. When compared at similarly hypotensive doses, flosequinan, in contrast to milrinone, isoprenaline and forskolin, did not influence ischaemia-induced arrhythmias or raise ventricular cyclic nucleotide levels in the anesthetized rat.

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Year:  1993        PMID: 8097953      PMCID: PMC1908168          DOI: 10.1111/j.1476-5381.1993.tb13513.x

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


  16 in total

1.  Mechanisms contributing to malignant dysrhythmias induced by ischemia in the cat.

Authors:  P B Corr; F X Witkowski; B E Sobel
Journal:  J Clin Invest       Date:  1978-01       Impact factor: 14.808

2.  A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samples.

Authors:  M A Markwell; S M Haas; L L Bieber; N E Tolbert
Journal:  Anal Biochem       Date:  1978-06-15       Impact factor: 3.365

3.  The relationship between coronary artery occlusion-induced arrhythmias and myocardial cyclic nucleotide levels in the anaesthetized rat.

Authors:  K A Kane; E J Morcillo-Sanchez; J R Parratt; I W Rodger; M Shahid
Journal:  Br J Pharmacol       Date:  1985-01       Impact factor: 8.739

4.  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

5.  Cyclic AMP mediated arrhythmias induced in the ischaemic pig heart.

Authors:  T Podzuweit; D J Els; J McCarthy
Journal:  Basic Res Cardiol       Date:  1981 Jul-Aug       Impact factor: 17.165

6.  Development of a severe model of early coronary artery ligation-induced dysrhythmias in the anaesthetized rat.

Authors:  R J Marshall; A W Muir; E Winslow
Journal:  Br J Pharmacol       Date:  1981-08       Impact factor: 8.739

7.  The genesis of arrhythmias during myocardial ischemia. Dissociation between changes in cyclic adenosine monophosphate and electrical instability in the rat.

Authors:  A S Manning; K Kinoshita; E Buschmans; D J Coltart; D J Hearse
Journal:  Circ Res       Date:  1985-11       Impact factor: 17.367

8.  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

9.  Effect of phosphodiesterase inhibitors on survival of patients with chronic congestive heart failure.

Authors:  M Packer
Journal:  Am J Cardiol       Date:  1989-01-03       Impact factor: 2.778

10.  Effect of flosequinan upon isoenzymes of phosphodiesterase from guinea-pig cardiac and vascular smooth muscle.

Authors:  G Frodsham; R B Jones
Journal:  Eur J Pharmacol       Date:  1992-02-18       Impact factor: 4.432

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  1 in total

1.  Failure of nitric oxide donors to alter arrhythmias induced by acute myocardial ischaemia or reperfusion in anaesthetized rats.

Authors:  C S Barnes; S J Coker
Journal:  Br J Pharmacol       Date:  1995-01       Impact factor: 8.739

  1 in total

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