Murakami Keiko, Ishida Kumiko, Watakabe Kyoko, Tsubouchi Ryoko, Naruse Makoto, Yoshino Masataka
Department of Biochemistry, Aichi Medical University School of Medicine, Yazako, Nagakute, Aichi 480-1195, Japan.
Toxicol Lett. 2006 Feb 20;161(2):102-7. doi: 10.1016/j.toxlet.2005.08.002. Epub 2005 Sep 6.
Apoptosis of HL60 cells by maltol was analyzed in relation to the maltol/iron-mediated generation of reactive oxygen species. Addition of maltol with FeSO(4) induced an apoptotic cell death as judged by flow cytometry analysis and DNA fragmentation on electrophoresis, but maltol or iron alone did not affect the cells. Treatment of HL60 cells with maltol/iron complex caused an effective inactivation of aconitase the most sensitive enzyme to reactive oxygen species. Maltol/iron-mediated apoptosis and the inactivation of aconitase was prevented by TEMPOL, the scavenger of reactive oxygen species. These findings suggest that maltol/iron complex can generate reactive oxygen species by the redox cycling, resulting in an apoptosis of HL60 cells. Cytotoxicity of maltol can be explained by the prooxidant properties of this compound.
分析了麦芽酚诱导HL60细胞凋亡与麦芽酚/铁介导的活性氧生成之间的关系。通过流式细胞术分析和电泳DNA片段化判断,麦芽酚与硫酸亚铁(FeSO₄)共同添加可诱导凋亡性细胞死亡,但单独的麦芽酚或铁对细胞无影响。用麦芽酚/铁复合物处理HL60细胞会导致乌头酸酶有效失活,乌头酸酶是对活性氧最敏感的酶。活性氧清除剂TEMPOL可阻止麦芽酚/铁介导的凋亡和乌头酸酶失活。这些发现表明,麦芽酚/铁复合物可通过氧化还原循环产生活性氧,从而导致HL60细胞凋亡。麦芽酚的细胞毒性可通过该化合物的促氧化特性来解释。