Search resultsModerate alcohol consumption reduces urinary 8-hydroxydeoxyguanosine by inducing of uric acid
Title
Moderate alcohol consumption reduces urinary 8-hydroxydeoxyguanosine by inducing of uric acid
Publication type
Journal Article
Year of Publication
2001
Authors
Journal
Industrial Health
Volume
39
Issue
4
Pagination
322 - 329
Date published
2001
ISBN
00198366 (ISSN)
Keywords
8 hydroxydeoxyguanosine, 8-Hydroxydeoxyguanosine, Adult, alanine aminotransferase, alcohol, alcohol consumption, Alcohol Drinking, Analysis of Variance, article, aspartate aminotransferase, Biological Markers, Biopyrrins, cancer risk, cardiovascular risk, deoxyguanosine, Dipyrone, DNA, DNA damage, Female, human, Humans, ischemic heart disease, male, Middle Aged, Oxidation-Reduction, oxidative stress, Questionnaires, reactive oxygen metabolite, Reactive Oxygen Species, uric acid
Abstract
Recent studies suggest that moderate alcohol consumption is associated with a low risk of cancer, coronary heart disease, and other diseases. Most of these diseases are considered to be related to the action of reactive oxygen species (ROS) at certain stages of disease progression. However, considerable evidence exists indicating that ethanol generates ROS in vivo. Thus, the reduced risk of disease as a result of alcohol consumption seems to contradict evidence suggesting the induction of ROS by ethanol. In the present study, we investigated whether oxidative stress was induced in moderate alcohol drinkers. We measured the total urinary biopyrrins and 8-hydroxydeoxyguanosine (8-OHdG) levels as a systemic oxidative stress marker and an oxidative DNA damage marker, respectively. Serum uric acid was also measured as an alcohol-induced antioxidant. We compared total urinary biopyrrins and 8-OHdG levels among groups with different alcohol habits. The results showed that total biopyrrins levels increased with the amount of alcohol consumed, but that the level of 8-OHdG significantly decreased with the amount of alcohol consumed. The decrease in 8-OHdG levels seemed to be associated with increasing levels of uric acid. Judging from the increasing level of total biopyrrins, alcohol may induce ROS. ROS may then cause cell damage in liver, as suggested by the positive correlation between the total biopyrrins levels and the serum GOT, GPT, and γ-GTP levels. However, since ROS may be more effectively counteracted by uric acid in organs other than the liver, DNA damage may be surpressed rather than induced. Accordingly, moderate alcohol consumption seems to have the overall effect of reducing DNA damage, as shown by the decrease in urinary 8-OHdG levels observed in our study.