Protection Against Oxidative Damage and Cell Death by the Natural Antioxidant Ergothioneine

Abstract

The natural antioxidant ergothioneine (EGT) was tested for its ability to inhibit cell death caused by hydrogen peroxide (H 2O 2) and to inhibit DNA oxidation by peroxynitrite (ONOO −) in human neuronal hybridoma cell line (N-18-RE-105). High concentrations of EGT (5 m m) were tolerated by the N-18-RE-105 cells. N-acetylcysteine (NAC) was not well tolerated by the cells at concentrations greater than 3 m m (cell viability averaged 50%). Increasing concentrations of EGT increases cell viability in the presence of NAC. EGT at concentrations up to 2 m m weakly improved cell viability in the presence of H 2O 2. NAC at concentrations up to 2 m m weakly decreased, but not significantly, the viability of the cells. At a higher concentration of 5 m m, NAC weakly protected the neuronal cells against the H 2O 2-induced cell death. The protection was significantly enhanced by preincubation with EGT. Ergothioneine inhibited ONOO −-induced oxidative damage in isolated calf thymus DNA and DNA in N-18-RE-105 cells. The concentration of EGT in human and mammalian tissue has been estimated to be 1–2 m m, which suggests that EGT may serve as a non-toxic thiol buffering antioxidant in vivo and may find applications in pharmaceutical preparations where oxidative stability is desired.