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J Am Coll Cardiol, 2003; 42:1299-1305, doi:10.1016/S0735-1097(03)00992-6
© 2003 by the American College of Cardiology Foundation
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Effect of tumor necrosis Factor-Alphaon endothelial and inducible nitric oxidesynthase messenger ribonucleic acidexpression and nitric oxide synthesisin ischemic and nonischemic isolated rat heart

Yosef Paz, MD*, Inna Frolkis, MD, PhD*,*, Dimitri Pevni, MD*, Itzhak Shapira, MD*, Yael Yuhas, PhD{ddagger}, Adrian Iaina, MD{dagger}, Yoram Wollman, PhD{dagger}, Tamara Chernichovski, MSc{dagger}, Nahum Nesher, MD*, Chaim Locker, MD*, Rephael Mohr, MD* and Gideon Uretzky, MD*

* Department of Thoracic and Cardiovascular Surgery, Tel-Aviv University, Tel-Aviv, Israel
{dagger} Department of Nephrology, Tel-Aviv Medical Center, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel
{ddagger} Felsenstein Medical Research Center, Petah-Tikva, Israel



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Figure 1 Effects of global cardioplegic ischemia on myocardial tumor necrosis factor-{alpha} (TNF-{alpha}) (A), endothelial nitric oxide synthase (eNOS) (B), and inducible nitric oxide synthase (iNOS) (C) mRNA expression: relative optical densities of polymerase chain reaction signals. Data were normalized to the glyceraldehyde 3-phosphate dehydrogenase (GAPDH) polymerase chain reaction signal. Shown are samples of left ventricular myocardium withdrawn at the end of stabilization [1], after ischemia [2], after ischemia with anti-TNF-{alpha} antibodies in the cardioplegia [3], and after 90 min of normal nonischemic perfusion [4].

 


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Figure 2 Effect of exogenous tumor necrosis factor-{alpha} on hemodynamic performance of isolated rat hearts during 1 h of perfusion: control group (open circles) and hearts treated with tumor necrosis factor-{alpha} (black circles), p < 0.0001 (analysis of variance) for all measurements vs. control.

 


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Figure 3 Effect of exogenous tumor necrosis factor-{alpha} on myocardial endothelial nitric oxide synthase (eNOS) (A) and inducible nitric oxide synthase (iNOS) (B) messenger ribonucleic acid expression: relative optical densities of polymerase chain reaction signals. Data were normalized to glyceraldehyde 3-phosphate dehydrogenase (GAPDH) polymerase chain reaction signal. Samples of left ventricular myocardium withdrawn at the end of stabilization [1], after 1-h perfusion with normal Krebs-Henseleit solution [2], and after 1 h of perfusion with tumor necrosis factor-{alpha} [3].

 




 
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