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Effects of red wine and vodka on collateral-dependent perfusion and cardiovascular function in hypercholesterolemic swine.

AbstractBACKGROUND:
Moderate consumption of alcohol, particularly red wine, has been shown to decrease cardiac risk. We used a hypercholesterolemic swine model of chronic ischemia to examine the effects of 2 alcoholic beverages on the heart.
METHODS AND RESULTS:
Yorkshire swine fed a high-cholesterol diet underwent left circumflex ameroid constrictor placement to induce chronic ischemia at 8 weeks of age. One group (HCC, n=9) continued on the diet alone, the second (HCW, n=8) was supplemented with red wine (pinot noir, 12.5% alcohol, 375 mL daily), and the third (HCV, n=9) was supplemented with vodka (40% alcohol, 112 mL daily). After 7 weeks, cardiac function was measured, and ischemic myocardium was harvested for analysis of perfusion, myocardial fibrosis, vessel function, protein expression, oxidative stress, and capillary density. Platelet function was measured by aggregometry. Perfusion to the ischemic territory as measured by microsphere injection was significantly increased in both HCW and HCV compared with HCC at rest, but in only the HCW group under ventricular pacing. Microvessel relaxation response to adenosine 5'-diphosphate was improved in the HCW group alone as was regional contractility in the ischemic territory, although myocardial fibrosis was decreased in both HCW and HCV. Expression of proangiogenic proteins phospho-endothelial nitric oxide synthase and vascular endothelial growth factor was increased in both HCW and HCV, whereas phospho-mammalian target of rapamycin was increased only in the HCV group. Expression of Sirt-1 and downstream antioxidant phospho-FoxO1 was increased only in the HCW group. Protein oxidative stress was decreased in the HCW group alone, whereas capillary density was increased only in the HCV group. There was no significant difference in platelet function between groups.
CONCLUSION:
Moderate consumption of red wine and vodka may reduce cardiovascular risk by improving collateral-dependent perfusion through different mechanisms. Red wine may offer increased cardioprotection related to its antioxidant properties.
AuthorsLouis M Chu, Antonio D Lassaletta, Michael P Robich, Yuhong Liu, Thomas Burgess, Roger J Laham, Joseph D Sweeney, Tun-Li Shen, Frank W Sellke
JournalCirculation (Circulation) Vol. 126 Issue 11 Suppl 1 Pg. S65-72 (Sep 11 2012) ISSN: 1524-4539 [Electronic] United States
PMID22965995 (Publication Type: Comparative Study, Evaluation Study, Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Vascular Endothelial Growth Factor A
  • Ethanol
  • Nitric Oxide Synthase Type III
  • TOR Serine-Threonine Kinases
Topics
  • Alcoholic Beverages
  • Animals
  • Cardiac Pacing, Artificial
  • Collateral Circulation
  • Coronary Circulation
  • Coronary Vessels (pathology)
  • Diet, Atherogenic
  • Disease Models, Animal
  • Endothelium, Vascular (physiopathology)
  • Enzyme Induction
  • Ethanol (blood)
  • Gene Expression Regulation
  • Hemodynamics
  • Hypercholesterolemia (complications, physiopathology, therapy)
  • Male
  • Models, Cardiovascular
  • Myocardial Ischemia (complications, physiopathology, therapy)
  • Nitric Oxide Synthase Type III (biosynthesis, genetics)
  • Oxidative Stress
  • Sus scrofa
  • Swine
  • TOR Serine-Threonine Kinases (biosynthesis, genetics)
  • Vascular Endothelial Growth Factor A (biosynthesis, genetics)
  • Wine

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