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SB 211475, a metabolite of carvedilol, reduces infarct size after myocardial ischemic and reperfusion injury in rabbits.

Abstract
The aim of this study was to investigate the effect of SB 211475, a metabolite of carvedilol with weak alpha1-adrenoceptor antagonism and antioxidant effect, on myocardial reperfusion injury and infarct size in anesthetized rabbits. The rabbits were subjected to 60 min of regional myocardial ischemia and 180 min of reperfusion. SB 211475 was administered either as 0.3, 1.0 or 3.0 mg/kg and compared to vehicle and carvedilol (1 mg/kg) treated animals. The lowest dose of SB 211475 (0.3 mg/kg) did not reduce infarct size compared to vehicle, whereas SB 211475 1.0 or 3.0 mg/kg reduced infarct size significantly compared to vehicle (41.2 +/- 2.2% and 40.5 +/- 2.8% vs. 59.1 +/- 3.9%, p < 0.05). Carvedilol reduced infarct size significantly more than SB 211475 1.0 and 3.0 mg/kg (28.8 +/- 3.9% vs. 41.2 +/- 2.2% and 40.5 +/- 2.7%, p < 0.05). Carvedilol and SB 211475 1.0 and 3.0 mg/kg reduced myeloperoxidase activity to the same extent, indicative of reduced inflammation. Rate-pressure product did not differ between doses of SB 211475. In conclusion, SB 211475 in the two highest doses reduced infarct size by protecting from reperfusion injury, possibly by reduced neutrophil accumulation. The superior cardiac protective effect of carvedilol over SB 211475 are most likely due to its adrenergic pharmacology including non-selective beta- and alpha1-adrenoceptor antagonism.
AuthorsH Brunvand, G Liu, X L Ma, T L Yue, R R Ruffolo Jr, G Z Feuerstein
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 356 Issue 2-3 Pg. 193-8 (Sep 04 1998) ISSN: 0014-2999 [Print] Netherlands
PMID9774249 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Adrenergic alpha-Antagonists
  • Antioxidants
  • Carbazoles
  • Propanolamines
  • Carvedilol
  • SB 211475
  • Peroxidase
Topics
  • Adrenergic alpha-Antagonists (therapeutic use)
  • Animals
  • Antioxidants (administration & dosage, therapeutic use)
  • Carbazoles (administration & dosage, therapeutic use)
  • Carvedilol
  • Dose-Response Relationship, Drug
  • Hemodynamics (drug effects)
  • Male
  • Myocardial Infarction (drug therapy)
  • Myocardial Reperfusion Injury (drug therapy, prevention & control)
  • Peroxidase (metabolism)
  • Propanolamines (administration & dosage, therapeutic use)
  • Rabbits

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