| Autor: |
Yang XM; 1 Department of Physiology and Cell Biology, University of South Alabama College of Medicine, Mobile, AL, USA., Downey JM; 1 Department of Physiology and Cell Biology, University of South Alabama College of Medicine, Mobile, AL, USA., Cohen MV; 1 Department of Physiology and Cell Biology, University of South Alabama College of Medicine, Mobile, AL, USA.; 2 Department of Medicine, University of South Alabama College of Medicine, Mobile, AL, USA., Housley NA; 3 Department of Microbiology and Immunology, University of South Alabama College of Medicine, Mobile, AL, USA.; 4 Center for Lung Biology, University of South Alabama College of Medicine, Mobile, AL, USA., Alvarez DF; 1 Department of Physiology and Cell Biology, University of South Alabama College of Medicine, Mobile, AL, USA.; 4 Center for Lung Biology, University of South Alabama College of Medicine, Mobile, AL, USA., Audia JP; 3 Department of Microbiology and Immunology, University of South Alabama College of Medicine, Mobile, AL, USA.; 4 Center for Lung Biology, University of South Alabama College of Medicine, Mobile, AL, USA. |
| Abstrakt: |
Use of ischemic postconditioning and other related cardioprotective interventions to treat patients with acute myocardial infarction (AMI) has failed to improve outcomes in clinical trials. Because P2Y 12 inhibitors are themselves postconditioning mimetics, it has been postulated that the loading dose of platelet inhibitors routinely given to patients treated for AMI masks the anti-infarct effect of other intended cardioprotective interventions. To further improve outcomes of patients with AMI, an intervention must be able to provide additive protection in the presence of a P2Y 12 platelet inhibitor. Previous studies reported an anti-infarct effect using a peptide inhibitor of the pro-inflammatory caspase-1 in animal models of AMI. Herein we tested whether a pharmacologic caspase-1 inhibitor can further limit infarct size in open-chest, anesthetized rats treated with a P2Y 12 inhibitor. One hour occlusion of a coronary branch followed by 2 hours of reperfusion was used to simulate clinical AMI and reflow. One group of rats received an intravenous bolus of 16 mg/kg of the highly selective caspase-1 inhibitor VX-765 30 minutes prior to onset of ischemia. A second group received a 60 µg/kg intravenous bolus of the P2Y 12 inhibitor cangrelor 10 minutes prior to reperfusion followed by 6 µg/kg/min continuous infusion. A third group received treatment with both inhibitors as above. Control animals received no treatment. Infarct size was measured by tetrazolium stain and volume of muscle at risk by fluorescent microspheres. In untreated hearts, 73.7% ± 4.1% of the ischemic zone infarcted. Treatment with either cangrelor or VX-765 alone reduced infarct size to 43.8% ± 2.4% and 39.6% ± 3.6% of the ischemic zone, respectively. Combining cangrelor and VX-765 was highly protective, resulting in only 14.0% ± 2.9% infarction. The ability of VX-765 to provide protection beyond that of a platelet inhibitor alone positions it as an attractive candidate therapy to further improve outcomes in today's patients with AMI. |
