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1.
J Cardiovasc Pharmacol ; 54(6): 468-76, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19770673

ABSTRACT

Epidemiological and experimental studies have revealed that a mild to moderate drinking of wine, particularly red wine, attenuates the cardiovascular, cerebrovascular, and peripheral vascular risk. However, the experimental basis for such health benefits is not fully understood. The cardioprotective effect of wine has been attributed to both components of wine: the alcoholic portion and, more importantly, the alcohol-free portion containing antioxidants. Wines are manufactured from grapes, which also contain a large variety of antioxidants, including resveratrol, catechin, epicatechin, and proanthocyanidins. Resveratrol is mainly found in the grape skin, whereas proanthocyanidins are found only in the seeds. Recent studies have demonstrated that resveratrol and proanthocyanidin are the major compounds present in grapes and wines responsible for cardioprotection. The purpose of this review is to provide evidence that grapes, wines, and resveratrol are equally important in reducing the risk of morbidity and mortality due to cardiovascular complications. Both wines and grapes can attenuate cardiac diseases such as atherosclerosis and ischemic heart disease. Recently, wine was also found to increase life span by inducing longevity genes. It appears that resveratrol and proanthocyanidins, especially resveratrol, present in grapes and wines play a crucial role in cardioprotective abilities of grapes and wines.


Subject(s)
Heart Diseases/prevention & control , Stilbenes/pharmacology , Vitis/chemistry , Wine/analysis , Cardiotonic Agents/pharmacokinetics , Cardiotonic Agents/pharmacology , Humans , Longevity/drug effects , Longevity/genetics , Resveratrol , Stilbenes/pharmacokinetics
2.
Free Radic Biol Med ; 46(5): 573-8, 2009 Mar 01.
Article in English | MEDLINE | ID: mdl-19071213

ABSTRACT

Resveratrol increases longevity through SirT1, which is activated with NAD(+) supplied by an anti-aging enzyme PBEF. SirT1 interacts with an anti-aging transcription factor, FoxO1, which is negatively regulated by Akt. Since white wine could have similar health benefits as red wine, we determined if white wine and its cardioprotective components possess anti-aging properties by feeding rats with these compounds. The hearts expressed SirT, FoxO, and PBEF in the order of white wine>resveratrol>tyrosol>hydroxytyrosol>red wine, while cardioprotection shown by reduction of infarct size and cardiomyocyte apoptosis followed a different pattern: resveratrol>red wine>hydroxytyrosol>white wine>tyrosol, suggesting the existence of different signaling mechanisms for the induction of longevity and survival.


Subject(s)
Cardiotonic Agents/administration & dosage , Phenylethyl Alcohol/analogs & derivatives , Reperfusion Injury/metabolism , Stilbenes/administration & dosage , Aging , Animals , Apoptosis/drug effects , Cardiotonic Agents/chemistry , Forkhead Transcription Factors/genetics , Forkhead Transcription Factors/metabolism , In Situ Nick-End Labeling , Myocytes, Cardiac/drug effects , Myocytes, Cardiac/metabolism , Myocytes, Cardiac/pathology , Nerve Tissue Proteins/genetics , Nerve Tissue Proteins/metabolism , Nicotinamide Phosphoribosyltransferase/genetics , Nicotinamide Phosphoribosyltransferase/metabolism , Oncogene Protein v-akt/genetics , Oncogene Protein v-akt/metabolism , Phenylethyl Alcohol/administration & dosage , Phenylethyl Alcohol/chemistry , Rats , Rats, Sprague-Dawley , Reperfusion Injury/pathology , Reperfusion Injury/prevention & control , Resveratrol , Signal Transduction , Sirtuins/genetics , Sirtuins/metabolism , Stilbenes/chemistry , Transcriptional Activation , Wine
3.
J Agric Food Chem ; 56(20): 9362-73, 2008 Oct 22.
Article in English | MEDLINE | ID: mdl-18821770

ABSTRACT

It is generally believed that the French paradox is related to the consumption of red wine and not other varieties of wine, including white wine or champagne. Some recent studies have indicated that white wine could also be as cardioprotective as red wine. The present investigation compares the cardioprotective abilities of red wine, white wine, and their principal cardioprotective constituents. Different groups of rats were gavaged with red wine, white wine, resveratrol, tyrosol, and hydroxytyrosol. Red wine and its constituent resveratrol and white wine and its constituents tyrosol and hydroxytyrosol all showed different degrees of cardioprotection as evidenced by their abilities to improve postischemic ventricular performance, reduce myocardial infarct size and cardiomyocyte apoptosis, and reduce peroxide formation. It was discovered in this study that although each of the wines and their components increased the enzymatic activities of the mitochondrial complex (I-IV) and citrate synthase, which play very important roles in oxidative phosphorylation and ATP synthesis, some of the groups were more complex-specific in inducing the activity compared to the other groups. Cardioprotective ability was further confirmed by increased expression of phospho-Akt, Bcl-2, eNOS, iNOS, COX-1, COX-2, Trx-1, Trx-2, and HO-1. The results of this study suggest that white wine can provide cardioprotection similar to red wine if it is rich in tyrosol and hydroxytyrosol.


Subject(s)
Cardiotonic Agents/pharmacology , Myocardial Ischemia/prevention & control , Phenylethyl Alcohol/analogs & derivatives , Stilbenes/pharmacology , Wine/analysis , Animals , Apoptosis , Apoptosis Regulatory Proteins/metabolism , Heart/physiology , Heart/physiopathology , Humans , In Vitro Techniques , Male , Mitochondrial Swelling/drug effects , Myocardial Ischemia/metabolism , Myocardial Ischemia/physiopathology , Myocardium/metabolism , Peroxides/metabolism , Phenylethyl Alcohol/pharmacology , Random Allocation , Rats , Rats, Sprague-Dawley , Resveratrol
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