Role of autacoids in cardiovascular colapse in anaphylactic shock in anaesthetized dogs

Cardiovasc Res. 1999 Jul;43(1):173-82. doi: 10.1016/s0008-6363(99)00073-5.

Abstract

Objective: In anaphylactic shock (AS), the relative effects of the autacoids including histamine, prostaglandins (prost), and leukotrienes (leuk) on causing cardiovascular collapse and the extent to which receptor blocking agents and pathway inhibitors may prevent this collapse are not clear.

Methods: In randomized design, we investigated whether blockade of histamine H1, H2, and H3 receptors or inhibition of the cyclooxygenase (cyclo) and lipoxygenase pathways (lipox) prevented AS in ragweed sensitized dogs. Seven dogs were studied under pentobarbital anesthesia in which the treatment studies were approximately 2 weeks apart.

Results: During H1 receptor blockade, the decreases in blood pressure and cardiac output otherwise observed in AS were attenuated (P < 0.05) and the release of prost, thromboxanes, and leuk were reduced as compared with nontreatment studies. Cyclo inhibition also attenuated cardiovascular collapse and mediator release in AS, but the other treatments showed no effects.

Conclusion: H1 receptor blockade and cyclo may attenuate cardiovascular shock in AS. These agents inhibit autacoid release from mast cells in addition to any specific receptor blocking and pathway inhibition effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Anaphylaxis / metabolism
  • Anaphylaxis / physiopathology
  • Anaphylaxis / prevention & control*
  • Animals
  • Cardiovascular System / physiopathology*
  • Cyclooxygenase Inhibitors / therapeutic use*
  • Dogs
  • Hemodynamics / drug effects
  • Histamine Antagonists / therapeutic use*
  • Histamine H1 Antagonists / therapeutic use
  • Histamine H2 Antagonists / therapeutic use
  • Indoles / therapeutic use
  • Indomethacin / therapeutic use
  • Inflammation Mediators / blood
  • Lipoxygenase Inhibitors / therapeutic use*
  • Piperidines / therapeutic use
  • Quinolines / therapeutic use
  • Random Allocation
  • Ranitidine / therapeutic use
  • Receptors, Histamine H3 / drug effects

Substances

  • Cyclooxygenase Inhibitors
  • Histamine Antagonists
  • Histamine H1 Antagonists
  • Histamine H2 Antagonists
  • Indoles
  • Inflammation Mediators
  • Lipoxygenase Inhibitors
  • Piperidines
  • Quinolines
  • Receptors, Histamine H3
  • MK 0591
  • Ranitidine
  • thioperamide
  • Indomethacin