Effect of N-acetyl- l-cysteine on ROS production and cell death caused by HEMA in human primary gingival fibroblasts

Abstract

Previous investigations have shown that 2-hydroxyethyl methacrylate (HEMA) causes reactive oxygen species (ROS) production, which in turn affects cell survival and cell death. The purpose of this study was to evaluate the effects of the antioxidant N-acetyl- l-cysteine (NAC) on HEMA-induced toxicity in human primary gingival fibroblasts (HGF). HGF were treated with various concentrations of HEMA (0–12 m m) in the absence and presence of NAC (1, 5, and 10 m m). The 3-(4,5 dimethyiazol-2-1)-2-5-diphenyl tetrazolium bromide (MTT) assay was used to evaluate the mitochondrial dehydrogenase activity after HEMA exposure. Viability and cell death were determined by flow cytometry using Annexin V and PI staining. ROS production was detected by the increasing fluorescence of the oxidation-sensitive dye 2′,7′-dichlorofluorescein diacetate (DCFH-DA) after HEMA treatment. After a 24 h incubation period, HEMA concentrations higher then 10 m m caused a decrease of cell viability, mitochondrial activity, and an increase of cell death. HEMA concentrations of 4–12 m m markedly increased ROS levels in a dose-dependent manner. High NAC concentrations (5 and 10 m m) significantly reduced cell death, and restored the mitochondrial activity after a 24 h co-treatment, but 1 m m NAC increased HEMA toxicity ( p<0.05). All NAC concentrations significantly reduced ROS levels induced by HEMA after a 2 h exposure ( p<0.05), but no such reduction was observed after a 4 h treatment. Furthermore, treatment with 10 m m HEMA and 1 m m NAC for 6 h caused an increase in ROS levels compared to 10 m m HEMA alone ( p<0.05). In conclusion, our results suggest that high NAC concentrations protect HGF against HEMA cytotoxicity by reducing the induced ROS levels.