@article{3128242,
    title = "Effects of l-NAME on coronary blood flow, infarct size and the extent of the no-reflow phenomenon",
    author = "Pierrakos, C.N. and Tsolakis, E.J. and Pozios, I.A. and Diakos, N. and Charitos, E. and Malliaras, K. and Bonios, M.J. and Lazaris, N. and Papazoglou, P. and Venetsanakos, J. and Papalois, A. and Terrovitis, J.V. and Nanas, J.N.",
    journal = "International Journal of Cardiology",
    year = "2013",
    volume = "167",
    number = "6",
    pages = "3000-3005",
    issn = "0167-5273",
    doi = "10.1016/j.ijcard.2012.09.013",
    keywords = "n(g) nitroarginine methyl ester;  nitric oxide synthase inhibitor, animal experiment;  animal model;  animal tissue;  aorta pressure;  article;  cardiovascular parameters;  continuous infusion;  controlled study;  coronary artery blood flow;  coronary reperfusion;  disease severity;  drug efficacy;  enzyme inhibition;  heart hemodynamics;  heart infarction;  heart infarction size;  heart muscle ischemia;  left anterior descending coronary artery;  loading drug dose;  myocardial area at risk;  no reflow phenomenon;  nonhuman;  priority journal;  swine, Acute myocardial infarction;  Cardiogenic shock;  Experimental study;  NOS inhibitors, Animals;  Blood Flow Velocity;  Coronary Circulation;  Enzyme Inhibitors;  Myocardial Infarction;  NG-Nitroarginine Methyl Ester;  No-Reflow Phenomenon;  Swine;  Treatment Outcome",
    abstract = "Background: NOS inhibitors are a potential treatment for patients with cardiogenic shock during acute myocardial infarction. Despite hemodynamic efficacy, their effects on the extent of myocardial infarction (MI) and the no-reflow phenomenon (NRP) have not been clarified. Methods: Sixteen pigs underwent occlusion of the mid left anterior descending coronary artery for 1 h followed by reperfusion for 2 h. Coronary blood flow (CBF), distal to the occlusion site, was measured. In eight experiments, l-NAME (non selective NO synthetase inhibitor) administration began 10 min before the onset of reperfusion and continued for 2 h (loading dose 1 mg/kg, perfusion rate: 1 mg/kg/h) (l-NAME group). Eight pigs received similarly normal saline (controls). At the end of each experiment, the myocardial area at risk (MAR) and extent of MI and NRP were measured. Results: Hemodynamics at baseline and during ischemia were similar in both groups. During reperfusion, the mean aortic blood pressure was significantly higher in the l-NAME group. In both groups, CBF reached a peak at 5 min of reperfusion, (no difference between groups). CBF gradually returned to baseline levels within 60 min of reperfusion in both groups. No statistically significant differences in the extent of the NRP (51.8 ± 19.7 vs 60.9 ± 11.4 p = 0.35) and MI (77.9 ± 13.9 vs 77.1 ± 8.8 p = 0.92), both expressed as a percentage of MAR, were observed between the l-NAME group and the control group. Conclusions: l-NAME administration started immediately before and maintained throughout reperfusion has no effect on NRP and MI size. l-NAME might stabilize patients with post-MI cardiogenic shock without adverse effects on infarct size. © 2012 Elsevier Ireland Ltd."
}