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Actions of non-cardiodepressant beta-adrenergic blocking agents in hemorrhagic shock.

Abstract
Two new beta-adrenergic blocking agents, timolol and MK-761, were found to effectively antagonize the positive inotropic effects of isoproterenol on isolated cat papillary muscles without depressing contractile force. However, appropriate doses of these beta-adrenergic blockers (ie, 12.5--25 microgram/kg) did not significantly prolong survival in hemorrhagic shock in anesthetized cats. MK-761 prevented some of the plasma accumulations of myocardial depressant factor (MDF) during shock. Nevertheless both beta-blockers failed to prevent the accumulation of the lysosomal protease cathepsin D or peptide fragments (ie, amino-nitrogen groups) in the blood during shock. We conclude that neither agent is of significant benefit in severe hemorrhagic shock, and probably beta-adrenergic blockade is not a productive approach to pursue in the therapeutics of hemorrhagic shock.
AuthorsA M Lefer, D J Lefer, R J Levin
JournalAdvances in shock research (Adv Shock Res) Vol. 3 Pg. 167-74 ( 1980) ISSN: 0195-878X [Print] United States
PMID6118024 (Publication Type: Journal Article)
Chemical References
  • Adrenergic beta-Antagonists
  • Myocardial Depressant Factor
  • Propanolamines
  • Pyridines
  • MK 761
  • Timolol
  • Isoproterenol
Topics
  • Adrenergic beta-Antagonists (therapeutic use)
  • Animals
  • Cats
  • In Vitro Techniques
  • Isoproterenol (pharmacology)
  • Male
  • Myocardial Contraction (drug effects)
  • Myocardial Depressant Factor
  • Propanolamines (therapeutic use)
  • Pyridines (pharmacology, therapeutic use)
  • Shock, Hemorrhagic (blood, drug therapy, physiopathology)
  • Timolol (pharmacology, therapeutic use)

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