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Submitted on March 26, 2004
From the Department of Internal Medicine and Therapeutics (S.S., H.A., T.M., S.T., H.O., M.F., A.H., Y.A., M.H.), Osaka University Graduate School of Medicine, Suita; the Department of Cardiovascular and Renal Medicine (K.N.), Saga University Faculty of Medicine, Saga; the Department of Physiological Science (Y.S.), Tokai University School of Medicine, Isehara; and the Cardiovascular Division of Medicine (A.O., J.K., H.M., H.T., S.K., M.K.), National Cardiovascular Center, Suita, Japan. * To whom correspondence should be addressed. E-mail: kitakaze{at}zf6.so-net.ne.jp.
Background--Although statins are reported to have a cardioprotective effect, their immediate direct influence on ischemia-reperfusion injury and the underlying mechanisms remain obscure. We investigated these issues an in vivo canine model. Methods and Results--Dogs were subjected to coronary occlusion (90 minutes) and reperfusion (6 hours) immediately after injection of pravastatin (0.2, 2, or 10 mg/kg), pitavastatin (0.01, 0.1, or 0.5 mg/kg), or cerivastatin (0.5, 5, or 50 µg/kg). Then myocardial phosphatidylinositol 3-kinase (PI3-K) and 5`-nucleotidase activities were measured, as well as infarct size. After 15 minutes of reperfusion, pravastatin caused dose-dependent activation of Akt and ecto-5`-nucleotidase in the ischemic zone, and the effect was significant at higher doses. Pitavastatin also significantly increased these activities, and its optimal dose was within the clinical range, whereas cerivastatin caused activation at the lowest dose tested. In all cases, both Akt and ecto-5`-nucleotidase showed activation in parallel, and this activation was completely abolished by wortmannin, a PI3-K inhibitor. The magnitude of the infarct-limiting effect paralleled the increase in Akt and ecto-5`-nucleotidase activity and was blunted by administration of wortmannin, Conclusions--Activation of ecto-5`-nucleotidase after ischemia by PI3-K activation may be crucial for immediate infarct-size limitation by statins. There seems to be an optimal dose for each statin that is independent of its clinical cholesterol-lowering effect.
Revised on May 4, 2004
Accepted on May 7, 2004
Optimal Windows of Statin Use for Immediate Infarct Limitation. 5'-Nucleotidase as Another Downstream Molecule of Phosphatidylinositol 3-Kinase
Shoji Sanada MD, PhD,
,
-methyleneadenosine-5`-diphosphate, or 8-sulfophenyltheophylline during reperfusion. Both collateral flow and the area at risk were comparable for all groups.
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