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J Am Coll Cardiol, 2003; 41:1183-1194, doi:10.1016/S0735-1097(03)00086-X
© 2003 by the American College of Cardiology Foundation
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Effect of aspirin on late preconditioning against myocardial stunning in conscious rabbits

Ken Shinmura, MD, PhD*, Eitaro Kodani, MD*, Y. u-Ting Xuan, PhD*, Buddhadeb Dawn, MD*, Xian-Liang Tang, MD* and Roberto Bolli, MD, FACC*,*

* Experimental Research Laboratory, Division of Cardiology, University of Louisville, and the Jewish Hospital Heart and Lung Institute, Louisville, Kentucky, USA



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Figure 1 Experimental protocols (protocol I): effect of acetylsalicylic acid (aspirin [ASA]) on late preconditioning (PC) against myocardial stunning. O = occlusion; R = reperfusion.

 


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Figure 2 Experimental protocols (protocols II and III): effect of acetylsalicylic acid (aspirin [ASA]) on platelet function. COX = cyclooxygenase; O = occlusion; R = reperfusion.

 


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Figure 3 Systolic thickening fraction in group I (control). Illustrated is thickening fraction at baseline, just before the first occlusion (Pre-O), 3 min into each coronary occlusion (O), 3 min into each reperfusion (R), and at selected times during the 5-h reperfusion period after the sixth occlusion. Thickening fraction is expressed as a percentage of baseline values. The two comparisons performed at each time-point from 5 min to 4 h of reperfusion were adjusted with the Bonferroni correction. Data are means ± SEM.

 


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Figure 4 Total deficit of systolic wall thickening after the sixth reperfusion. The total deficit of systolic wall thickening was measured in arbitrary units, as described in the text. The two comparisons performed in each group were adjusted by the Bonferroni correction. Data are means ± SEM. ASA = acetylsalicylic acid.

 


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Figure 5 Systolic thickening fraction in group II (low acetylsalicylic acid [aspirin {ASA}] on day 2) (A) and in group III (high ASA on day 1) (B). Same format as Figure 3. In both groups II and III, the two comparisons performed at each time-point from 5 min to 4 h of reperfusion were adjusted with the Bonferroni correction. Data are means ± SEM. Pre-O = before first occlusion; O/R = occlusion/reperfusion.

 


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Figure 6 Systolic thickening fraction in group IV (high acetylsalicylic acid [aspirin {ASA}] on day 2) (A) and in group V (multiple ASA) (B). Same format as Figure 3. In both groups IV and V, the two comparisons performed at each time-point from 5 min to 4 h of reperfusion were adjusted with the Bonferroni correction. Data are means ± SEM. Pre-O = before first occlusion; O/R = occlusion/reperfusion.

 


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Figure 7 (Upper panel) Representative Western immunoblots showing the expression of cyclooxygenase (COX-2) protein in the membranous fraction in the ischemic/reperfused region. (Lower panels) Densitometic analysis of COX-2 protein signals in the membranous fraction in the ischemic/reperfused region (anterior left ventricular [LV] wall) (left) and in the nonischemic region (posterior LV wall) (right). In all samples, the densitometric measurements of COX-2 immunoreactivity were expressed as a percentage of the average value measured in the corresponding LV wall of control rabbits. The two comparisons performed in each panel were adjusted by the Bonferroni correction. Data are means ± SEM. ASA = acetylsalicylic acid (aspirin); PC = preconditioning.

 


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Figure 8 Myocardial levels of prostaglandin (PG)E2 and 6-keto-PGF1{alpha} (measured by enzyme immunoassay). The three intergroup comparisons performed in each panel were adjusted by the Bonferroni correction. Data are means ± SEM. ASA = acetylsalicylic acid (aspirin); PC = preconditioning.

 




 
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