The ability of Vitamin C to affect genetic damage was reviewed in human studies that used molecular epidemiology methods, including analysis of DNA adducts, DNA strand breakage (using the Comet assay), oxidative damage measured as levels of 8-oxo-7,8-dihydroxy-2'-deoxyguanosine (8-oxodG), cytogenetic analysis of chromosomal aberrations and micronuclei, and the induction of DNA repair proteins. The protective effect of Vitamin C was observed at plasma levels>50?mol/l. Vitamin C supplementation decreased the frequency of chromosomal aberrations in groups with insufficient dietary intake who were occupationally exposed to mutagens, and also decreased the sensitivity to mutagens as assessed using the bleomycin assay. High Vitamin C levels in plasma decreased the frequency of genomic translocations in groups exposed to ionizing radiation or c-PAHs in polluted air. The frequency of micronuclei was decreased by Vitamin C supplementation in smokers challenged with ?-irradiation, and higher Vitamin C levels in plasma counteracted the damage induced by air pollution. The prevalence of DNA adducts inversely correlated with Vitamin C levels in groups environmentally exposed to high concentrations of c-PAHs. Increased Vitamin C levels decreased DNA strand breakage induced by air pollution. Oxidative damage (8-oxodG levels) was decreased by Vitamin C supplementation in groups with plasma levels>50?mol/l exposed to PM2.5 and c-PAHs. Modulation of DNA repair by vitamin C supplementation was observed both in poorly nourished subjects and in groups with Vitamin C plasma levels>50?mol/l exposed to higher concentrations of c-PAHs. It is possible that the impact of Vitamin C on DNA damage depends both on background values of Vitamin C in the individual as well as on the level of exposure to xenobiotics or oxidative stress.
Share or Bookmark this page: You will need to have an account with the selected service in order to post links or bookmark this page.