Genotoxic effect induced by hydrogen peroxide in human hepatoma cells using comet assay

Background: Hydrogen peroxide is a common reactive oxygen intermediate generated by variousforms of oxidative stress. Aims: The aim of this study was to investigate the DNA damage capacity ofH2O2 in HepG2 cells. Methods: Cells were treated with H2O2 at concentrations of 25 μM or 50 μM for5 min, 30 min, 40 min, 1 h or 24 h in parallel. The extent of DNA damage was assessed by the cometassay. Results: Compared to the control, DNA damage by 25 μM and 50 μM H2O2 increasedsignificantly with increasing incubation time up to 1 h, but it was not increased at 24 h. Conclusions:Our Findings confirm that H2O2 is a typical DNA damage inducing agent and thus is a good modelsystem to study the effects of oxidative stress. DNA damage in HepG2 cells increased significantlywith H2O2 concentration and time of incubation but later decreased likely due to DNA repairmechanisms and antioxidant enzyme

Instream Large Wood: Denitrification Hotspots with Low N 2

We examined the effect of instream large wood on denitrification capacity in two contrasting, lower order streams - one that drains an agricultural watershed with no riparian forest and minimal stores of instream large wood and another that drains a forested watershed with an extensive riparian forest and abundant instream large wood. We incubated two types of wood substrates (fresh wood blocks and extant streambed wood) and an artificial stone substrate for nine weeks in each stream. After in situ incubation, we collected the substrates and their attached biofilms and established laboratory-based mesocosm assays with stream water amended with 15N-labeled nitrate-N. Wood substrates at the forested site had significantly higher denitrification than wood substrates from the agricultural site and artificial stone substrates from either site. Nitrate-N removal rates were markedly higher on woody substrates compared to artificial stones at both sites. Nitrate-N removal rates were significantly correlated with biofilm biomass. Denitrification capacity accounted for only a portion of nitrate-N removal observed within the mesocosms in both the wood controls and instream substrates. N2 accounted for 99.7% of total denitrification. Restoration practices that generate large wood in streams should be encouraged for N removal and do not appear to generate high risks of instream N2O generation. © 2014 American Water Resources Association