Department of Anesthesiology and Pain Medicine, Seoul National University Bundang Hospital, Gyeonggi-do, Republic of Korea.
Spinal Cord. 2012 Mar;50(3):208-12. doi: 10.1038/sc.2011.136. Epub 2011 Nov 29.
Experimental study.
To investigate the effect of erythropoietin (EPO) pretreatment on spinal cord ischemic injury.
Experimental Research Center at Seoul National University Bundang Hospital, Korea.
Rats were treated with either 1000 IU kg(-1) of EPO (EPO group, n=8) or saline (control group, n=8) 24 h before ischemia. Spinal cord ischemia was induced using a balloon-tipped catheter placed on the proximal descending aorta in the control group and the EPO group, but not in the sham group (n=8). Neurological function was assessed using the motor deficit index (MDI; 0=normal, 6=complete paralysis) until 7 days after reperfusion, and histological examination of spinal cord was performed.
At the first day after reperfusion, the EPO group demonstrated a significantly lower MDI compared with the control group (2.0 (0.3-2.0) vs 4.0 (3.0-4.8), median (interquartile range); EPO group vs control group, respectively; P=0.002). This trend was sustained until 7 days after reperfusion (1.0 (1.0-1.8) vs 4.5 (3.3-5.0); EPO group vs control group, respectively; P=0.001), and more normal motor neurons (29.9±3.1 vs 21.4±3.4, mean±s.d.; EPO group vs control group, respectively; P<0.001) were observed. However, compared with the sham group, the EPO group displayed a significantly higher MDI (0.0, sham group) and fewer intact motor neurons (37.8±5.5, sham group; P<0.001, sham vs control group).
Pretreatment with EPO significantly attenuates neurological injury following spinal cord ischemia, although it cannot completely abolish the ischemic injury.
实验研究。
研究促红细胞生成素(EPO)预处理对脊髓缺血性损伤的影响。
韩国首尔国立大学盆唐医院实验研究中心。
将大鼠分为 EPO 组(n=8)和对照组(n=8),EPO 组于缺血前 24 h 给予 1000 IU·kg(-1)EPO,对照组给予生理盐水。对照组和 EPO 组通过气囊导管置于降主动脉近端诱导脊髓缺血,但假手术组(n=8)不进行缺血处理。采用运动缺陷指数(MDI;0=正常,6=完全瘫痪)评估神经功能,直至再灌注后 7 天,并进行脊髓组织学检查。
再灌注后第 1 天,EPO 组 MDI 明显低于对照组(2.0(0.3-2.0)比 4.0(3.0-4.8),中位数(四分位数间距);EPO 组比对照组;P=0.002)。这一趋势持续到再灌注后 7 天(1.0(1.0-1.8)比 4.5(3.3-5.0),EPO 组比对照组;P=0.001),且观察到更多正常运动神经元(29.9±3.1 比 21.4±3.4,EPO 组比对照组;P<0.001)。然而,与假手术组相比,EPO 组的 MDI 明显升高(0.0,假手术组),完整运动神经元减少(37.8±5.5,假手术组;P<0.001,假手术组比对照组)。
EPO 预处理可显著减轻脊髓缺血后的神经损伤,但不能完全消除缺血性损伤。