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The effect of cyclo-oxygenase and thromboxane synthetase inhibitors on shock induced by injection of heterologous blood in cats.

Abstract
The injection of rabbit blood into cats causes hypotension, thrombocytopaenia, leukopaenia, a rise in central venous pressure and right ventricular and pulmonary artery pressures and a fall in circulating levels of fibrinogen. Death occurred rapidly after injection of the rabbit blood in 50% of control animals and was associated with respiratory distress. Measurement of plasma thromboxane B2 and 6-oxo PGF1 alpha levels in surviving controls demonstrated a marked elevation in the former with no significant change in the latter. Pretreatment with either the thromboxane synthetase inhibitor, 1-(cyclo octyl methyl) imidazole or aspirin prevented respiratory distress and death and reduced or prevented the elevations in cardiovascular pressures observed in control animals. Neither compound prevented thrombocytopaenia or leukopaenia but did attenuate the rise of thromboxane B2 following injection of rabbit blood. In addition, pretreatment with 1-(cyclo octyl methyl) imidazole resulted in an approximately five-fold increase in circulatory levels of 6-oxo PGF1 alpha five minutes after inducing the shock. We conclude that thromboxane A2 plays an important role in pulmonary (and other organs) dysfunction during the shock induced by injection of heterologous blood. In addition we have shown that inhibition of thromboxane synthetase in vivo under conditions where thromboxane A2 is produced leads to an increase in the synthesis of prostacyclin.
AuthorsS Bunting, S Castro, J A Salmon, S Moncada
JournalThrombosis research (Thromb Res) Vol. 30 Issue 6 Pg. 609-17 (Jun 15 1983) ISSN: 0049-3848 [Print] United States
PMID6412392 (Publication Type: Journal Article)
Chemical References
  • Cyclooxygenase Inhibitors
  • Prostaglandins
  • Oxidoreductases
  • Thromboxane-A Synthase
Topics
  • Animals
  • Blood Group Incompatibility (complications)
  • Cats
  • Cyclooxygenase Inhibitors
  • Female
  • Male
  • Oxidoreductases (antagonists & inhibitors)
  • Prostaglandins (biosynthesis)
  • Rabbits
  • Shock (etiology, metabolism, physiopathology)
  • Thromboxane-A Synthase (antagonists & inhibitors)

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