Department of Virology, Institute for Medical Microbiology and Hygiene, University of Freiburg, Freiburg, Germany.
Anticancer Res. 2010 Oct;30(10):3967-79.
Salen-manganese complexes, such as EUK-8 and EUK-134 are known as catalase mimetics with superoxide dismutase (SOD) and peroxidase mimetic activity. Here we show that the concentration-dependent use of salen-manganese complexes within the appropriate time window and with parallel control of signaling parameters allows complex interactions during intercellular induction of apoptosis to be studied. At very low concentrations, salen-manganese complexes can abrogate consumption reactions between HOCl and hydrogen peroxide, as well as NO and hydrogen peroxide, and thus the major signaling pathways are enhanced. At higher concentrations of the compounds, all major signaling pathways are inhibited, thereby the catalase mimetic activity of the compounds affects both hydrogen peroxide and peroxynitrite. The ratio between available hydrogen peroxide and salen-manganese complexes defines whether reactive oxygen species (ROS) effects are inhibited or apoptosis is induced by the compounds. The SOD mimetic activity of salen-manganese complexes seems to be insufficient to interfere with intercellular ROS signaling.
Salen-锰配合物,如 EUK-8 和 EUK-134,是已知的过氧化氢酶模拟物,具有超氧化物歧化酶(SOD)和过氧化物酶模拟活性。在这里,我们表明,在适当的时间窗口内,锰配合物的浓度依赖性使用,并与信号参数的平行控制,允许在细胞间诱导细胞凋亡的复杂相互作用进行研究。在非常低的浓度下,salen-锰配合物可以阻止 HOCl 和过氧化氢之间、以及 NO 和过氧化氢之间的消耗反应,从而增强主要的信号通路。在化合物的较高浓度下,所有主要的信号通路都被抑制,从而化合物的过氧化氢酶模拟活性影响过氧化氢和过氧亚硝酸盐。可用的过氧化氢和 salen-锰配合物之间的比例决定了化合物对活性氧物质(ROS)的影响是抑制还是诱导细胞凋亡。salen-锰配合物的 SOD 模拟活性似乎不足以干扰细胞间的 ROS 信号。