Cardioprotective effect of liposomal prostaglandin E1 on a porcine model of myocardial infarction reperfusion no-reflow

Objective: To evaluate whether liposomal prostaglandin E1 (lipo-PGE1) can decrease reperfusion no-reflow in a catheter-based porcine model of acute myocardial infarction (AMI). Methods: Twenty-two male Chinese mini-swines were randomized into three groups: six in a sham-operation group, and eight ea...

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Veröffentlicht in:Journal of Zhejiang University. B. Science 2011-08, Vol.12 (8), p.638-643
Hauptverfasser: Li, Jia-hui, Yang, Peng, Li, Ai-li, Wang, Yong, Ke, Yuan-nan, Li, Xian-lun
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Sprache:eng
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Zusammenfassung:Objective: To evaluate whether liposomal prostaglandin E1 (lipo-PGE1) can decrease reperfusion no-reflow in a catheter-based porcine model of acute myocardial infarction (AMI). Methods: Twenty-two male Chinese mini-swines were randomized into three groups: six in a sham-operation group, and eight each in the control and lipo-PGE1 groups. The distal part of the left anterior descending coronary artery (LAD) in the latter two groups was completely occluded for 2 h, and then reperfused for 3 h. Lipo-PGE1 (1 pg/kg) was injected 10 min before LAD occlusion until reperfusion for 1 h in the lipo-PGE1 group. Hemodynamic data and proinflammatory cytokines were examined before AMI, 2 h after occlusion, and 1, 2, and 3 h after reperfusion. Myocardial contrast echocardiography (MCE) and double staining were performed to evaluate the myocardial no-reflow area (NRA). Results: Left ventricular systolic pressure and end-diastolic pressure significantly improved in the lipo-PGE1 group after reperfusion compared with the control group and also 2 h after AMI (P〈0.05 for both). MCE and double staining both showed that lipo-PGE1 decreased reperfusion NRA after AMI (P〈0.05, P〈0.01). Lipo-PGE1 decreased serum interleukin-6 (IL-6) and tumor necrosis factor-a (TNF-a) after myocardial infarction reperfusion (P〈0.05 for both). Conclusions: Lipo-PGE1 is cardioprotective in our porcine model of myocardial infarction reperfusion no-reflow, decreasing NRA and attenuating the inflammatory response.
ISSN:1673-1581
1862-1783
DOI:10.1631/jzus.B1101007