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J Am Coll Cardiol, 2001; 37:608-615
© 2001 by the American College of Cardiology Foundation
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Hypercholesterolemia impairs myocardial perfusion and permeability: role of oxidative stress and endogenous scavenging activity

Martin Rodriguez-Porcel, MD*, Amir Lerman, MD*, Patricia J. M. Best, MD*, James D. Krier, MS{dagger}, Claudio Napoli, MD, PhD{ddagger} § and Lilach O. Lerman, MD, PhD{dagger}

* Department of Internal Medicine, Division of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA
{dagger} Division of Hypertension, Mayo Clinic, Rochester, Minnesota, USA
{ddagger} Department of Medicine, University of Naples, Naples, Italy
§ Department of Medicine-0682, University of California, San Diego, California, USA



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Figure 1 (A) Tomographic cross-sectional image of the heart at the level of the mid-LV, showing a traced anterior wall region-of-interest, and contrast media in the LV cavity. (B) Time-density curves consequent to transit of contrast media through the anterior cardiac wall region of interest (closed circles), depicting the modeling of intra- and extra-vascular curves (triangle and square symbols, respectively). LV = left ventricle.

 


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Figure 2 Top panel: Relative change (percent compared with baseline) of anterior wall myocardial perfusion in response to IV adenosine in normal pigs (n = 8), hypercholesterolemic pigs (HC, n = 8), and HC pigs that received dietary antioxidant supplementation (HC + AO, n = 6). Bottom panel: Relative change (percent compared with baseline) of anterior wall microvascular permeability index in response to IV adenosine in normal, HC and HC + AO pigs. *p < 0.05 compared with normal and HC + AO pigs. HC = hypercholesterolemia; HC + AO = HC plus long-term vitamin supplementation.

 


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Figure 3 Top panel: Correlation between the change in myocardial perfusion in response to adenosine in hypercholesterolemic (HC) pigs and vitamin-treated HC pigs with tissue (right) and systemic (left)) levels of vitamins E (open circles) and C (closed circles). Bottom panel: Correlation between the change in microvascular permeability in response to adenosine in HC and vitamin-treated HC pigs with tissue (right) and systemic (left) levels of vitamins E and C.

 




 
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