Tang L X, Yang J L, Shen X
Institute of Biophysics, Chinese Academy of Sciences, Beijing, People's Republic of China.
J Inorg Biochem. 1997 Dec;68(4):265-72. doi: 10.1016/s0162-0134(97)00107-4.
The addition of chelated Fe2+ ions in a liposomal system often results in a short lag period before peroxidation starts. The addition of a second chelator at the end of the lag period results in an inhibition of the lipid peroxidation. The degree of inhibition depends on the stability constants of the chelator in ligating Fe2+ and/or Fe3+. A more striking inhibitory effect was observed for the chelators with higher stability constant for either or both Fe(2+)- and Fe(3+)-complex, but much less inhibition was found for those with lower stability constants for both complexes. Assuming that the "initiator" for iron-dependent lipid peroxidation is formed through the redox process of iron ion and finally emerged at the end of the latent period, the inhibitory effect of the second chelator may be explained as the abstraction of either Fe2+ or Fe3+ from the initiator by an additional free chelator, which results in the decomposition of the initiator. This study supports the hypothesis that a Fe2+ ... Fe3+ complex is responsible for iron-initiated lipid peroxidation.
在脂质体系统中添加螯合的Fe2+离子通常会导致在过氧化开始前有一个短暂的延迟期。在延迟期结束时添加第二种螯合剂会抑制脂质过氧化。抑制程度取决于螯合剂在结合Fe2+和/或Fe3+时的稳定常数。对于与Fe(2+) - 和Fe(3+) - 络合物具有较高稳定常数的螯合剂,观察到更显著的抑制作用,但对于两种络合物都具有较低稳定常数的螯合剂,抑制作用则小得多。假设铁依赖性脂质过氧化的“引发剂”是通过铁离子的氧化还原过程形成的,并最终在潜伏期结束时出现,那么第二种螯合剂的抑制作用可以解释为额外的游离螯合剂从引发剂中提取Fe2+或Fe3+,这导致引发剂的分解。这项研究支持了Fe2+...Fe3+络合物是铁引发脂质过氧化的原因这一假设。