Shimoda Mitsugi, Sawada Tokihiko, Iwasaki Yoshimi, Mori Shozo, Kijima Hiroaki, Okada Toshie, Kubota Keiichi
Second Department of Surgery, Dokkyo University School of Medicine, Kitakobayashi 880, Mibu Shimotsuga 880, Tochigi 321-0293, Japan.
Hepatogastroenterology. 2009 Mar-Apr;56(90):470-5.
BACKGROUND/AIMS: We investigated, for the first time, the protective effect of erythropoietin (EPO) against liver ischemia-reperfusion (I-R) injury in a pig model.
Partial hepatic ischemia was maintained for 60 min in a pig. Pigs were allocated to 4 groups (n=5 each): (1) Control group with I-R injury (Vehicle); (2) EPO group with I-R injury, given three injections of EPO at 5000 IU/kg (EPO5000x3); (3) EPO group with I-R injury, given a single injection of EPO at 5000 IU/kg (EPO5000x1); and (4) EPO group with I-R injury, given three injections of EPO at 500 IU/kg (EPO500x3). Liver function tests (AST, ALT, LDH), and TUNEL assay were performed.
Three hours after I-R injury, AST levels in the Vehicle, EPO5000x3, EPO5000x1, and EPO500 x3 groups were 1494.2 +/- 711.3 U/L, 307.3 +/- 127.6 UL, 296.5 +/- 9.2 U/L, and 474.6 +/- 242.0 UL, respectively (one-factor ANOVA, p = 0.020). At 3h the ALT and LDH levels in the Vehicle group were significantly higher than those in the EPO5000x3 and EPO5000x1 groups. Apoptotic indices in the Vehicle, EPO500x3, EPO5000x1, and EPO500x3 groups 3 h after I-R injury were 2.40 +/- 0.93, 1.36 +/- 0.12, 1.11 +/- 0.17, and 1.51 +/- 0.33, respectively. The apoptotic indices of the EPO5000x1 and EPO500x3 groups were significantly lower than that of the Vehicle group.
EPO treatment significantly ameliorated liver I-R injury in this pig model. The protective effect was exerted by the inhibition of apoptosis. These results will open the door for the clinical application of EPO in liver surgery.
背景/目的:我们首次在猪模型中研究了促红细胞生成素(EPO)对肝脏缺血再灌注(I-R)损伤的保护作用。
在猪身上维持部分肝脏缺血60分钟。将猪分为4组(每组n = 5):(1)I-R损伤对照组(载体);(2)I-R损伤EPO组,给予3次5000 IU/kg的EPO注射(EPO5000x3);(3)I-R损伤EPO组,给予1次5000 IU/kg的EPO注射(EPO5000x1);(4)I-R损伤EPO组,给予3次500 IU/kg的EPO注射(EPO500x3)。进行肝功能测试(AST、ALT、LDH)和TUNEL分析。
I-R损伤后3小时,载体组、EPO5000x3组、EPO5000x1组和EPO500x3组的AST水平分别为1494.2±711.3 U/L、307.3±127.6 U/L、296.5±9.2 U/L和474.6±242.0 U/L(单因素方差分析,p = 0.020)。3小时时,载体组的ALT和LDH水平显著高于EPO5000x3组和EPO5000x1组。I-R损伤后3小时,载体组、EPO500x3组、EPO5000x1组和EPO500x3组的凋亡指数分别为2.40±0.93、1.36±0.12、1.11±0.17和1.51±0.33。EPO5000x1组和EPO500x3组的凋亡指数显著低于载体组。
在该猪模型中,EPO治疗显著改善了肝脏I-R损伤。其保护作用是通过抑制细胞凋亡实现的。这些结果将为EPO在肝脏手术中的临床应用打开大门。