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Am J Physiol Heart Circ Physiol 292: H2891-H2897, 2007. First published February 2, 2007; doi:10.1152/ajpheart.01269.2006
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Aspirin before reperfusion blunts the infarct size limiting effect of atorvastatin

Yochai Birnbaum,1,3 Yu Lin,1 Yumei Ye,1 Juan D. Martinez,2 Ming-He Huang,1 Charles Y. Lui,1 Jose R Perez-Polo,3 and Barry F. Uretsky1

1Division of Cardiology, 2Department of Internal Medicine; 3Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas

Submitted 20 November 2006 ; accepted in final form 1 February 2007

We assessed whether aspirin (acetylsalicylic acid, ASA), administered before reperfusion, abrogates the infarct size (IS)-limiting effect of atorvastatin (ATV). Statins reduce IS. This dose-dependent effect is mediated by upregulation of cycloxygenase-2 (COX2) and PGI2 production. Administration of selective COX2-inhibitors either with ATV for 3 days or immediately before coronary occlusion blocks the IS-limiting effect of ATV. Sprague-Dawley rats received 3-day ATV (10 mg·kg–1·day–1) or water alone. Rats underwent 30 min coronary artery occlusion and 4 h reperfusion (IS protocol, n = 8 in each group), or rats underwent 30 min coronary artery occlusion and 10 min reperfusion (enzyme expression and activity protocol, n = 4 in each group). Immediately before reperfusion rats received intravenous ASA (5, 10, or 20 mg/kg) or saline. Area-at-risk (AR) was assessed by blue dye and IS by triphenyltetrazolium chloride. ATV reduced IS (10.1 ± 1.4% of the AR) compared with controls (31.0 ± 2.2%). Intravenous ASA alone did not affect IS (29.0 ± 2.6%); however, ASA dose dependently (5, 10, and 20 mg/kg) attenuated the protective effect of ATV on IS (15.8 ± 0.9%, 22.0 ± 1.6%, and 23.7 ± 3.8%, respectively). ASA dose dependently blocked the upregulation of COX2 by ATV. COX2 activity was as follows: control, 8.93 ± 0.90 pg/mg; ATV, 75.85 ± 1.08 pg/mg; ATV + ASA5, 34.39 ± 1.48 pg/mg; ATV + ASA10, 19.87 ± 1.10 pg/mg; and ATV + ASA20, 9.36 ± 0.94 pg/mg. ASA, administered before reperfusion in doses comparable to those used in the clinical setting, abrogates the IS-limiting effect of ATV in a model with mechanical occlusion of the coronary artery. This potential adverse interaction should be further investigated in the clinical setting of acute coronary syndromes.

acetylsalicylic acid; cyclooxygenase-2



Address for reprint requests and other correspondence: Y. Birnbaum, Division of Cardiology, Univ. of Texas Medical Branch, 5,106 John Sealy Annex, 301 Univ. Blvd., Galveston, Texas 77555-0553 (e-mail: yobirnba{at}utmb.edu)




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Am. J. Physiol. Heart Circ. Physiol.Home page
Y. Ye, Y. Lin, R. Perez-Polo, M.-H. Huang, M. G. Hughes, D. J. McAdoo, S. Manickavasagam, B. F. Uretsky, and Y. Birnbaum
Enhanced cardioprotection against ischemia-reperfusion injury with a dipyridamole and low-dose atorvastatin combination
Am J Physiol Heart Circ Physiol, July 1, 2007; 293(1): H813 - H818.
[Abstract] [Full Text] [PDF]




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