Effect of white wine consumption on oxidative stress markers and homocysteine levels
Language English Country Czech Republic Media print-electronic
Document type Controlled Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
PubMed
16555941
DOI
10.33549/physiolres.930936
PII: 0936
Knihovny.cz E-resources
- MeSH
- Apolipoproteins blood MeSH
- Aryldialkylphosphatase blood MeSH
- Biomarkers blood MeSH
- C-Reactive Protein metabolism MeSH
- Cholesterol blood MeSH
- Adult MeSH
- Glutathione blood MeSH
- Glutathione Peroxidase blood MeSH
- Homocysteine blood MeSH
- Liver enzymology MeSH
- Cardiovascular Diseases blood etiology metabolism MeSH
- Cohort Studies MeSH
- Thiobarbituric Acid Reactive Substances metabolism MeSH
- Humans MeSH
- Oxidative Stress * MeSH
- Alcohol Drinking blood metabolism MeSH
- Risk Factors MeSH
- Superoxide Dismutase blood MeSH
- Triglycerides blood MeSH
- Wine * MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Controlled Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Apolipoproteins MeSH
- Aryldialkylphosphatase MeSH
- Biomarkers MeSH
- C-Reactive Protein MeSH
- Cholesterol MeSH
- Glutathione MeSH
- Glutathione Peroxidase MeSH
- Homocysteine MeSH
- Thiobarbituric Acid Reactive Substances MeSH
- PON1 protein, human MeSH Browser
- Superoxide Dismutase MeSH
- Triglycerides MeSH
The aim of this study was to assess the influence of regular daily consumption of white wine on oxidative stress and cardiovascular risk markers. Forty-two healthy male volunteers consumed 375 ml of white wine daily. Each participant provided three venous blood samples (before wine consumption, following the wine consumption period and again a month later). Levels of superoxide dismutase, glutathione peroxidase, reduced glutathione, total antioxidant capacity, total cholesterol, HDL-cholesterol, apolipoprotein A I, apolipoprotein B, triglycerides, paraoxonase 1, C-reactive protein, homocysteine, thiobarbituric acid reactive substances (TBARS) and advanced oxidation protein products (AOPP) were measured. Immediately following the month of white wine consumption there was a significant increase in HDL-cholesterol (p<0.0001), paraoxonase 1 (p<0.001), glutathione peroxidase (p<0.001) and reduced glutathione (p<0.01) levels, a decrease in superoxide dismutase activities (p<0.0001), and a decrease in oxidation protein products (p<0.001) and TBARS (p<0.05) concentrations. However, there was also a clear increase in homocysteine (p<0.0001) after a month of white wine consumption. The results of our non-placebo controlled trial suggest that regular daily white wine consumption is associated not only with both antioxidative and antiatherogenic effects but also with a potentially proatherogenic increase of homocysteine concentrations.
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