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Am J Physiol Heart Circ Physiol 293: H813-H818, 2007. First published April 6, 2007; doi:10.1152/ajpheart.00210.2007
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Enhanced cardioprotection against ischemia-reperfusion injury with a dipyridamole and low-dose atorvastatin combination

Yumei Ye,1 Yu Lin,1 Regino Perez-Polo,2 Ming-He Huang,1 Michael G. Hughes,3 David J. McAdoo,3 Saraswathy Manickavasagam,1 Barry F. Uretsky,1 and Yochai Birnbaum1,2

1Division of Cardiology and Departments of 2Biochemistry and Molecular Biology and 3Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, Texas

Submitted 16 February 2007 ; accepted in final form 3 April 2007

Atorvastatin (ATV) limits infarct size (IS) by activating Akt and ecto-5-nucleotidase, which generates adenosine. Activated Akt and adenosine activate endothelial nitric oxide synthase (eNOS). When given orally, high doses (10 mg/kg) are needed to achieve full protection. We determined whether dipyridamole (DIP), by preventing the reuptake of adenosine, has a synergistic effect with ATV in reducing myocardial IS. In this study, rats received 3-days of the following: water, ATV (2 mg·kg–1·day–1), DIP (6 mg·kg–1·day–1), or ATV + DIP. In addition, rats received 3-days of the following: aminophylline (Ami; 10 mg·kg–1·day–1) or Ami + ATV + DIP. Rats underwent 30 min of myocardial ischemia followed by 4 h of reperfusion (IS protocol), or hearts were explanted for immunoblotting. As a result, IS in the controls was 34.0 ± 2.8% of the area at risk. ATV (33.1 ± 2.1%) and DIP (30.5 ± 1.5%) did not affect IS, whereas ATV + DIP reduced IS (12.2 ± 0.5%; P < 0.001 vs. each of the other groups). There was no difference in IS between the Ami alone (48.1 ± 0.8%) and the Ami + ATV + DIP (45.8 ± 2.9%) group (P = 0.422), suggesting that Ami completely blocked the protective effect. Myocardial adenosine level in the controls was 30.6 ± 3.6 pg/µl. ATV (51.0 ± 4.9 pg/µl) and DIP (51.5 ± 6.8 pg/µl) caused a small increase in adenosine levels, whereas ATV + DIP caused a greater increase in adenosine levels (66.4 ± 3.1 pg/µl). ATV and DIP alone did not affect myocardial Ser473 phosphorylated-Akt and Ser1177 phosphorylated-eNOS levels, whereas ATV + DIP significantly increased them. In conclusion, low-dose ATV and DIP had synergistic effects in reducing myocardial IS and activation of Akt and eNOS. This combination may have a potential benefit in augmenting the eNOS-mediated pleiotropic effects of statins.

adenosine; Akt; infarct size; nitric oxide synthase



Address for reprint requests and other correspondence: Y. Birnbaum, Div. of Cardiology, Univ. of Texas Medical Branch, 5.106 John Sealy Annex, 301 Univ. Blvd., Galveston, TX 77555-0553 (e-mail: yobirnba{at}utmb.edu)




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