Institute of Medical Sciences, Tzu Chi University, Hualien, Taiwan.
Injury. 2010 Jul;41(7):724-30. doi: 10.1016/j.injury.2009.12.006. Epub 2009 Dec 31.
Erythropoietin (EPO) has pleiotropic cytoprotective actions. We investigated the effects of EPO on the physiopathology and cytokine levels after haemorrhagic shock (HS) in conscious rats.
Rats received an intravenous injection of 300 U/kg EPO over 10 min followed by HS via withdrawal of 60% of total blood volume from a femoral arterial catheter (6 ml/100 g body weight) over 30 min. Mean arterial pressure (MAP) and heart rate (HR) were monitored continuously for 18 h after the start of blood withdrawal. Levels of biochemical parameters, including haemoglobin, GOT, GPT, BUN, creatinine (Cr), LDH, CPK, and lactate were measured at 30 min before the induction of HS and 0, 1, 3, 6, 9, 12, and 18 h after HS. Cytokine levels, including TNF-alpha and IL-6, in serum were measured at 1, 9, and 18 h after HS. The kidneys, liver, lungs, and small intestine were removed for pathology assessment at 48 h after HS.
HS significantly increased HR, blood GOT, GPT, BUN, Cr, LDH, CPK, lactate, TNF-alpha, and IL-6 levels and decreased haemoglobin and MAP in rats. Pre-treatment with EPO improved survival rate, preserved the MAP, decreased the tachycardia and markers of organ injury, suppressed the release of TNF-alpha and IL-6 after HS in rats.
Pre-treatment with EPO suppresses the release of serum TNF-alpha and IL-6, along with decreasing the levels of markers of organ injury associated with HS, with such actions ameliorating HS-induced organ damage in rats.
促红细胞生成素(EPO)具有多种细胞保护作用。我们研究了 EPO 对清醒大鼠失血性休克(HS)后病理生理学和细胞因子水平的影响。
大鼠在 10 分钟内静脉注射 300 U/kg EPO,然后通过从股动脉导管(6 ml/100 g 体重)中抽取 60%的总血量,在 30 分钟内完成 HS。从抽血开始后 18 小时内,连续监测平均动脉压(MAP)和心率(HR)。在 HS 诱导前 30 分钟和 HS 后 0、1、3、6、9、12 和 18 小时测量包括血红蛋白、GOT、GPT、BUN、肌酐(Cr)、LDH、CPK 和乳酸在内的生化参数水平。在 HS 后 1、9 和 18 小时测量血清中细胞因子水平,包括 TNF-α和 IL-6。在 HS 后 48 小时,取出肾脏、肝脏、肺和小肠进行病理评估。
HS 显著增加了大鼠的 HR、血液 GOT、GPT、BUN、Cr、LDH、CPK、乳酸、TNF-α和 IL-6 水平,并降低了血红蛋白和 MAP。EPO 预处理提高了生存率,维持了 MAP,降低了心动过速和器官损伤标志物,抑制了 HS 后大鼠血清 TNF-α和 IL-6 的释放。
EPO 预处理抑制了血清 TNF-α和 IL-6 的释放,同时降低了与 HS 相关的器官损伤标志物水平,从而改善了 HS 诱导的大鼠器官损伤。