Obolensky Alexey, Berenshtein Eduard, Konijn Abraham M, Banin Eyal, Chevion Mordechai
Department of Ophthalmology, The Hebrew University-Hadassah Schools of Medicine and Dental Medicine, Jerusalem 91120, Israel.
Free Radic Biol Med. 2008 Apr 1;44(7):1286-94. doi: 10.1016/j.freeradbiomed.2007.10.060. Epub 2007 Nov 21.
Ischemic preconditioning (IPC) of the retina, accomplished by ischemia of short duration, is highly effective in preventing subsequent severe injury caused by iron-dependent free radical burst after prolonged ischemia. To investigate the mechanistic basis for IPC rescue, we examined changes in the levels of the retinal redox-active and labile iron pool, ferritin, and ferritin-bound iron. Prolonged ischemia severely impaired retinal function, with total loss of the full-field electroretinographic response. IPC provided marked protection against such injury. Histological examination revealed that ischemia-associated structural damage and loss of cells in the outer and inner nuclear layers were largely prevented by IPC. Ferritin levels decreased after prolonged ischemia but remained close to normal when the ischemic episode was preceded by IPC. The protective effect of IPC on retinal function and ferritin was blocked by a zinc-desferrioxamine complex known to interfere with iron signaling. The results suggest a mechanism whereby IPC activates an iron signaling pathway leading to a marked increase in ferritin levels, which mediates resistance to prolonged ischemia.
通过短暂缺血实现的视网膜缺血预处理(IPC),在预防长时间缺血后由铁依赖性自由基爆发引起的后续严重损伤方面非常有效。为了研究IPC保护作用的机制基础,我们检测了视网膜氧化还原活性和不稳定铁池、铁蛋白以及铁蛋白结合铁水平的变化。长时间缺血严重损害视网膜功能,全视野视网膜电图反应完全丧失。IPC对这种损伤提供了显著的保护作用。组织学检查显示,IPC在很大程度上预防了缺血相关的结构损伤以及外核层和内核层细胞的丢失。长时间缺血后铁蛋白水平降低,但在缺血发作前进行IPC时,铁蛋白水平仍接近正常。已知一种锌去铁胺复合物会干扰铁信号传导,它能阻断IPC对视网膜功能和铁蛋白的保护作用。结果提示了一种机制,即IPC激活一条铁信号通路,导致铁蛋白水平显著升高,从而介导对长时间缺血的抵抗。