Department of General Surgery, Kocatepe University, Afyon, Turkey.
HPB (Oxford). 2004;6(3):169-73. doi: 10.1080/13651820410026077.
Besides its haematopoietic effect, erythropoietin (EPO) has multiple protective effects, i.e. antiapoptotic, antioxidant and angiogenic properties. The neuroprotective effects of EPO against ischaemia have all been demonstrated in cell culture and animal models. The aim of the study was to evaluate the effect of erythropoietin on ischaemia-reperfusion injury (I/R injury) of the liver.
Forty-eight adult male Sprague-Dawley rats weighing 250-300 g were divided into three groups: group I, hepatic ischaemia-reperfusion (Hepatic I/R); group II, hepatic ischaemia-reperfusion + EPO (Hepatic I/R+ EPO); group III, sham. Hepatic ischaemia was created by placing a microvascular clamp on the hepatic pedicle for 45 minutes. EPO was given to group II at a dose of 1000 U/kg 120 minutes before the onset of the ischaemia. Blood samples and liver tissues were obtained after 45 minutes of reperfusion from half of the rats in each group. The remaining rats were killed after a 24-hour observation period and blood and tissue samples were obtained. Blood alanine aminotransferase, tumour necrosis factor-alpha (TNF-alpha), interleukin-2 (IL-2) and liver tissue malondialdehyde (MDA) levels were determined. Liver tissue histopathology was also evaluated by light microscopy.
In rats with hepatic ischaemia, serum levels of ALT, TNF-alpha, IL-2 and liver tissue levels of MDA were reduced by the administration of erythropoietin and the histopathological score was also less severe.
This study demonstrates that pre-ischaemic administration of EPO has protective effects on hepatic I/R injury.
除了造血作用外,促红细胞生成素(EPO)还具有多种保护作用,即抗凋亡、抗氧化和血管生成特性。EPO 对缺血的神经保护作用已在细胞培养和动物模型中得到证实。本研究旨在评估促红细胞生成素对肝脏缺血再灌注损伤(I/R 损伤)的影响。
48 只成年雄性 Sprague-Dawley 大鼠,体重 250-300g,分为三组:I 组,肝缺血再灌注(Hepatic I/R);II 组,肝缺血再灌注+EPO(Hepatic I/R+EPO);III 组,假手术。通过在肝蒂上放置微血管夹 45 分钟来创建肝缺血。在缺血开始前 120 分钟,给 II 组大鼠注射 1000U/kg 的 EPO。从每组的一半大鼠中获得再灌注 45 分钟后的血液样本和肝组织。其余大鼠在 24 小时观察期后处死,并获得血液和组织样本。测定血液丙氨酸转氨酶、肿瘤坏死因子-α(TNF-α)、白细胞介素-2(IL-2)和肝组织丙二醛(MDA)水平。通过光镜评估肝组织病理学。
在肝缺血的大鼠中,促红细胞生成素的给药降低了血清 ALT、TNF-α、IL-2 和肝组织 MDA 水平,组织学评分也较轻。
本研究表明,缺血前给予 EPO 对肝 I/R 损伤具有保护作用。