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Increase of the ventricular fibrillation threshold by 711389-S, a new antiarrhythmic agent, in guinea-pigs.

Abstract
The increase of the ventricular fibrillation threshold (VFT) by 711389-S, a new antiarrhythmic agent, was compared with several other antiarrhythmic drugs using both in vitro (Langendorff) and in vivo preparations of guinea-pigs. The doses of antiarrhythmic drugs for increasing VFT by 10 volts in in vitro (microgram) and in vivo (mg/kg, i.v.) preparations were as follows: 711389-S: 4.2, 0.15; disopyramide: 32.6, 0.86; quinidine: 32.0, 0.57; aprindine: 7.6, 0.55; propranolol: 16.6, 0.57; and lidocaine: 20.7, 1.52. The duration of the antifibrillatory effects of 711389-S almost corresponded with those of aprindine and propranolol.
AuthorsS Nakajima, M Ueda
JournalJapanese journal of pharmacology (Jpn J Pharmacol) Vol. 38 Issue 4 Pg. 436-8 (Aug 1985) ISSN: 0021-5198 [Print] Japan
PMID3840850 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Anti-Arrhythmia Agents
  • Propanolamines
  • 711389-S
Topics
  • Action Potentials (drug effects)
  • Animals
  • Anti-Arrhythmia Agents (pharmacology)
  • Dose-Response Relationship, Drug
  • Guinea Pigs
  • Heart (drug effects)
  • In Vitro Techniques
  • Male
  • Propanolamines (pharmacology)
  • Ventricular Fibrillation (physiopathology)

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