Coronary thrombolytic properties of a novel recombinant plasminogen activator (BM 06.022) in a canine model

J Cardiovasc Pharmacol. 1991 Jul;18(1):111-9. doi: 10.1097/00005344-199107000-00015.

Abstract

We studied the thrombolytic dose-response relationship of a recombinant plasminogen activator (rPA) (BM 06.022) compared with alteplase in a canine model of coronary artery thrombosis. BM 06.022 consists of the kringle 2 and protease domains of human tissue PA (tPA) and lacks oligosaccharide side chains because of its expression in Escherichia coli. Thrombus formation in anesthetized, open-chest dogs was induced by electrical injury to the intimal surface of the left circumflex coronary artery in the presence of a critical stenosis. Intravenous bolus injection of BM 06.022 (50, 100, 140, and 200 kU/kg) or of alteplase (200, 800, 1,130, and 1,600 kU/kg) 30 min after coronary occlusion to six heparinized dogs per group achieved a dose-dependent increase in reperfusion rate and decrease in residual thrombus wet weight. Vehicle-treated dogs did not reperfuse. Semilogarithmic regression analysis showed that the effective dose that produced 50% reperfusion of BM 06.022 (83 kU/kg) was 11.6-fold lower than that of alteplase (951 kU/kg). Comparison with infusion experiments showed that intravenous bolus injection of 140 kU/kg of BM 06.022 was equieffective to a 90-min infusion of 800 kU/kg (= 1 mg/kg) of alteplase as a standard treatment regarding reperfusion rate (66%) and time to reperfusion (15 +/- 6 vs. 18 +/- 8 min). Pharmacokinetic analysis for functionally active BM 06.022 or alteplase in plasma revealed a total plasma clearance of 4.1-6.6 ml/min/kg for BM 06.022 and of 12.6-42.3 ml/min/kg for alteplase.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH terms

  • Anesthesia
  • Animals
  • Bleeding Time
  • Coronary Circulation / drug effects*
  • Dogs
  • Dose-Response Relationship, Drug
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Female
  • Fibrinogen / metabolism
  • Fibrinolytic Agents*
  • Hemostasis / drug effects
  • Male
  • Plasminogen / metabolism
  • Plasminogen Activators / genetics
  • Plasminogen Activators / pharmacokinetics
  • Plasminogen Activators / pharmacology*
  • Recombinant Proteins / pharmacology
  • Regression Analysis
  • Tissue Plasminogen Activator / pharmacology*
  • alpha-2-Antiplasmin / metabolism

Substances

  • Fibrinolytic Agents
  • Recombinant Proteins
  • alpha-2-Antiplasmin
  • Fibrinogen
  • Plasminogen
  • reteplase
  • Plasminogen Activators
  • Tissue Plasminogen Activator