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Acrolein toxicity: Comparison with reactive oxygen species
Authors:Madoka Yoshida  Hideyuki Tomitori  Motofumi Hagihara  Hitomi Goda  Masaru Niitsu  Kazuei Igarashi
Institution:a Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba 260-8675, Japan
b Amine Pharma Research Institute, 1-8-15 Inohana, Chuo-ku, Chiba 260-0856, Japan
c Faculty of Pharmacy, Chiba Institute of Science, 15-8 Shiomi-cho, Choshi, Chiba 288-0025, Japan
d Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado 350-0248, Japan
Abstract:The toxicity of acrolein was compared with that of reactive oxygen species using a mouse mammary carcinoma FM3A cell culture system. Complete inhibition of cell growth was accomplished with 10 μM acrolein, 100 μM H2O2, and 20 μM H2O2 plus 1 mM vitamin C, which produce radical dotOH, suggesting that toxicity of acrolein is more severe than H2O2 and nearly equal to that of radical dotOH, when these compounds were added extracellularly. Acrolein toxicity was prevented by N-acetyl-l-cysteine and N-benzylhydroxylamine, and attenuated by putrescine and spermidine. Toxicity of H2O2 was prevented by glutathione peroxidase plus N-acetyl-l-cysteine, pyruvate, catalase, and reduced by polyphenol, and toxicity of radical dotOH was prevented by glutathione peroxidase plus N-acetyl-l-cysteine, pyruvate, catalase and reduced by N-acetyl-l-cysteine. The results indicate that prevention of cell toxicity by N-acetyl-l-cysteine was more effective with acrolein than with radical dotOH. Protein and DNA synthesis was damaged primarily by acrolein and reactive oxygen species, respectively.
Keywords:Acrolein  Hydrogen peroxide  Hydroxyl radical  Polyamine  SH reagents  α-keto acids
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