Abstract
Mangiferin (MGN), a dietary C‐glucosylxanthone present in Mangifera indica, is known to possess a spectrum of beneficial pharmacological properties. This study demonstrates antigenotoxic potential of MGN against mercuric chloride (HgCl~2~) induced genotoxicity in HepG2 cell line. Treatment of HepG2 cells with various concentrations of HgCl~2~ for 3 h caused a dose‐dependent increase in micronuclei frequency and elevation in DNA strand breaks (olive tail moment and tail DNA). Pretreatment with MGN significantly (p < 0.01) inhibited HgCl~2~‐induced (20 µM for 30 h) DNA damage. An optimal antigenotoxic effect of MGN, both in micronuclei and comet assay, was observed at a concentration of 50 µM. Furthermore, HepG2 cells treated with various concentrations of HgCl~2~ resulted in a dose‐dependent increase in the dichlorofluorescein fluorescence, indicating an increase in the generation of reactive oxygen species (ROS). However, MGN by itself failed to generate ROS at a concentration of 50 µM, whereas it could significantly decrease HgCl~2~‐induced ROS. Our study clearly demonstrates that MGN pretreatment reduced the HgCl~2~‐induced DNA damage in HepG2 cells, thus demonstrating the genoprotective potential of MGN, which is mediated mainly by the inhibition of oxidative stress. © 2011 Wiley Periodicals, Inc. J Biochem Mol Toxicol 25:108–116 2011; View this article online at wileyonlinelibrary.com. DOI 10.1002/jbt.20366