Kidney Disease Center, Medical College of Wisconsin, 53226, USA.
Free Radic Res. 2010 Jul;44(7):773-82. doi: 10.3109/10715761003786164.
This study examined the time-dependent effects of a cell permeable SOD mimetic, MnTMPyP, on mitochondrial function in renal ischemia-reperfusion injury (IRI). Male SD rats were subject to either sham operation or bilateral renal ischemia for 45 min followed by reperfusion for 1, 4 or 24 h. A sub-set of animals was treated with either saline vehicle or 5 mg/Kg of MnTMPyP (i.p.). EPR measurements showed that at 1-h reperfusion MnTMPyP prevented a decrease in aconitase activity (p < 0.05) and attenuated the increase in the high spin heme at g = 6 and oxidation of 4Fe4S to 3Fe4S signal at g = 2.015 (p < 0.01). MnTMPyP was effective in preventing loss of mitochondrial complexes and prevented the loss of cytochrome c and Smac/Diablo from mitochondria early in reperfusion. Following 24 h of reperfusion MnTMPyP was effective in attenuating caspase-3 and blocking apoptosis (p < 0.05). In conclusion, MnTMPyP has biphasic effects in renal IRI, inhibiting mitochondrial dysfunction at the early phases of reperfusion and prevention of apoptosis following longer durations of reperfusion.
这项研究考察了一种细胞通透的 SOD 模拟物 MnTMPyP 对肾缺血再灌注损伤 (IRI) 中线粒体功能的时间依赖性影响。雄性 SD 大鼠接受假手术或双侧肾缺血 45 分钟,然后再灌注 1、4 或 24 小时。一部分动物接受生理盐水或 5mg/kg MnTMPyP(ip)治疗。EPR 测量显示,在再灌注 1 小时时,MnTMPyP 可防止柠檬酸合酶活性下降(p<0.05),并减弱 g=6 处高自旋血红素的增加和 g=2.015 处 4Fe4S 氧化为 3Fe4S 信号(p<0.01)。MnTMPyP 能有效防止线粒体复合物的丢失,并防止再灌注早期细胞色素 c 和 Smac/ Diablo 从线粒体中丢失。再灌注 24 小时后,MnTMPyP 能有效抑制 caspase-3 并阻止细胞凋亡(p<0.05)。总之,MnTMPyP 在肾 IRI 中具有双相作用,在再灌注早期抑制线粒体功能障碍,并在较长时间的再灌注后防止细胞凋亡。