Mitra Amit, Bansal Shweta, Wang Wei, Falk Sandor, Zolty Einath, Schrier Robert W
University of Colorado Health Sciences Center, 4200 East 9th Ave. Box C-281, Denver, CO 80262, USA.
Nephrol Dial Transplant. 2007 Aug;22(8):2349-53. doi: 10.1093/ndt/gfm216. Epub 2007 Apr 16.
Sepsis has a high mortality (50-80%) when associated with acute renal failure (ARF). Oxidant injury and proinflammatory cytokines and chemokines have been shown to increase with endotoxaemia-related ARF. Since erythropoietin (EPO) has been demonstrated to possess anti-oxidant and anti-inflammatory properties, EPO may have therapeutic efficacy for treating ARF associated with endotoxaemia.
Wild-type mice were given 2.5 mg/kg of intraperitoneal (i.p.) endotoxin, lipopolysaccharide (LPS), and studied 16 h later. Thirty minutes prior to LPS, the mice were given either EPO or vehicle.
During endotoxaemia, EPO was found to significantly attenuate the renal dysfunction, as assessed by glomerular filtration rate (48.1 +/- 12.4 microl/min vs 136.7 +/- 30.2, P < 0.05). Renal blood flow and mean arterial pressure were not significantly different between the two groups. The renal dysfunction during endotoxaemia was associated with a decrease in renal superoxide dismutase (SOD). The EPO-related renal protection was associated with reversal of the effects of endotoxin on renal SOD.
This is the first demonstration of a renal protective effect of EPO on endotoxin-related renal dysfunction.
脓毒症与急性肾衰竭(ARF)相关时具有较高的死亡率(50 - 80%)。氧化损伤以及促炎细胞因子和趋化因子已被证明在内毒素血症相关的急性肾衰竭中会增加。由于促红细胞生成素(EPO)已被证明具有抗氧化和抗炎特性,EPO可能对治疗与内毒素血症相关的急性肾衰竭具有治疗效果。
给野生型小鼠腹腔注射(i.p.)2.5 mg/kg内毒素、脂多糖(LPS),并在16小时后进行研究。在给予LPS前30分钟,给小鼠注射EPO或赋形剂。
在内毒素血症期间,通过肾小球滤过率评估发现,EPO能显著减轻肾功能障碍(48.1 ± 12.4微升/分钟对136.7 ± 30.2,P < 0.05)。两组之间的肾血流量和平均动脉压无显著差异。内毒素血症期间的肾功能障碍与肾超氧化物歧化酶(SOD)的降低有关。EPO相关的肾脏保护作用与内毒素对肾SOD作用的逆转有关。
这是首次证明EPO对与内毒素相关的肾功能障碍具有肾脏保护作用。