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首页> 外文期刊>Surgery >Erythropoietin and its derivative protect the intestine from severe ischemia/reperfusion injury in the rat.
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Erythropoietin and its derivative protect the intestine from severe ischemia/reperfusion injury in the rat.

机译:促红细胞生成素及其衍生物可保护肠道免受大鼠严重缺血/再灌注损伤。

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摘要

OBJECTIVE: To investigate the protective effect of erythropoietin (EPO) and its nonhematopoietic derivative (asialoEPO) against intestinal ischemia/reperfusion (I/R) injury in a rat model. METHODS: The superior mesenteric artery of Wistar rats was clamped for 60 minutes and then released. The rats were divided into 4 groups (n = 15 in each group): sham operation (Sham), vehicle treatment (Vehicle), EPO treatment (EPO), and asialoEPO treatment (AsialoEPO). EPO and asialoEPO were administered subcutaneously at 1000 units/kg for 10 minutes before clamping, 30 minutes after the start of clamping, and just before declamping. This treatment was followed by determination of 72-hour survival rates, serum TNF-alpha and IL-6 levels, histologic evaluation of the small intestine, quantification of the number of apoptotic cells, and analysis of the antiapoptotic molecules Bcl-xL and XIAP by Western blotting. RESULTS: The survival rates at 72 hours after I/R injury in the Sham, Vehicle, EPO, and AsialoEPO groups were 100%, 33%, 75%, and 83%, respectively (P < .05). Blood TNF-alpha and IL-6 were significantly more suppressed in the EPO and AsialoEPO groups than in the Vehicle group at 6 hours after I/R injury. Histologically, injury to villi in the EPO and AsialoEPO groups was significantly less than in the Vehicle group. The number of apoptotic cells in the EPO and AsialoEPO groups was significantly less than in the Vehicle group. Western blotting revealed that EPO and asialoEPO constitutively increased the expression of Bcl-xL. CONCLUSIONS: EPO and asialoEPO exert a strong protective effect against intestinal I/R injury, possibly by inhibiting release of TNF-alpha and IL-6 and decreasing apoptosis.
机译:目的:探讨促红细胞生成素(EPO)及其非造血衍生物(asialoEPO)对大鼠肠缺血/再灌注(I / R)损伤的保护作用。方法:将Wistar大鼠的肠系膜上动脉夹紧60分钟,然后释放。将大鼠分成4组(每组n = 15):假手术(Sham),媒介物治疗(车辆),EPO治疗(EPO)和无唾液酸EPO治疗(AsialoEPO)。钳夹前,钳夹开始后30分钟和钳夹之前,以1000单位/ kg的皮下注射EPO和无唾液酸EPO,持续10分钟。进行此治疗后,确定72小时生存率,血清TNF-α和IL-6水平,小肠的组织学评估,凋亡细胞数量的定量以及抗凋亡分子Bcl-xL和XIAP的分析。蛋白质印迹。结果:假手术,车辆,EPO和AsialoEPO组I / R损伤后72小时的存活率分别为100%,33%,75%和83%(P <.05)。在I / R损伤后6小时,EPO和AsialoEPO组的血液TNF-α和IL-6的抑制作用明显强于媒介物组。从组织学上讲,EPO和AsialoEPO组对绒毛的伤害显着少于Vehicle组。 EPO和AsialoEPO组的凋亡细胞数量显着少于赋形剂组。蛋白质印迹表明,EPO和无唾液酸EPO组成性地增加了Bcl-xL的表达。结论:EPO和去唾液酸化EPO可能通过抑制TNF-α和IL-6的释放并减少细胞凋亡而对肠I / R损伤具有很强的保护作用。

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