4.5 Article

Triple Therapy Greatly Increases Myocardial Salvage During Ischemia/Reperfusion in the in situ Rat Heart

期刊

CARDIOVASCULAR DRUGS AND THERAPY
卷 27, 期 5, 页码 403-412

出版社

SPRINGER
DOI: 10.1007/s10557-013-6474-9

关键词

Cangrelor; Cardioprotection; Cariporide; Hypothermia; Myocardial infarction; Platelet aggregation; Ticagrelor

资金

  1. Heart, Lung and Blood Institute of the National Institutes of Health [HL-20648]
  2. Otsuka Maryland Medicinal Labs., Inc., Rockville, MD

向作者/读者索取更多资源

Cangrelor, a P2Y(12) receptor blocker, administered just prior to reperfusion reduced but did not eliminate myocardial infarction in rabbits. Combining cangrelor with ischemic postconditioning offered no additional protection suggesting they protected by a similar mechanism. To determine if cangrelor's protection might be additive to other cardioprotective interventions we tested cangrelor in combination with ischemic preconditioning, cariporide, a sodium-hydrogen exchange blocker, and mild hypothermia. Open-chest rats underwent 30-min coronary occlusion/2-h reperfusion. Cangrelor, administered as a bolus (60 mu g/kg) 10 min before reperfusion and continued as an infusion (6 mu g/kg/min) for the duration of the experiment, decreased infarction from 45.3 % of risk zone in control hearts to 25.0 %. Combining cangrelor and ischemic preconditioning offered no additional protection. Mild hypothermia (32-33 A degrees C) instituted by peritoneal lavage with cold saline just prior to coronary occlusion resulted in 25.2 % infarction, and combining cangrelor and hypothermia nearly halved infarction to 14.1 % of risk zone. Cariporide (0.5 mg/kg) just prior to occlusion resulted in 27.2 % infarction and 15.8 % when combined with cangrelor. Combining cangrelor, hypothermia and cariporide further halved infarction to only 6.3 %. We also tested another P2Y(12) inhibitor ticagrelor which is chemically similar to cangrelor. Ticagrelor (20 mg/kg) fed 1 h prior to surgery reduced infarct size by an amount similar to that obtained with cangrelor (25.6 % infarction), and this protective effect was abolished by chelerythrine and wortmannin, thus implicating participation of PKC and PI3-kinase, resp., in signaling. Cardioprotection from a P2Y(12) receptor antagonist can be combined with at least 2 other strategies to magnify the protection. Combining multiple interventions that use different cardioprotective mechanisms could provide powerful protection against infarction in patients with acute coronary thrombosis.

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