首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Cold ischemia-reperfusion injury of the liver. Role of the liver donor nutritional status in rats.
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Cold ischemia-reperfusion injury of the liver. Role of the liver donor nutritional status in rats.

机译:肝脏冷缺血-再灌注损伤。肝脏供体营养状况在大鼠中的作用。

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摘要

To verify the role of donor nutritional status on the quality of liver preservation after cold storage, we assessed hepatocyte and liver endothelial cell viabilities and functions in an isolated perfused rat liver model. Livers from fed and fasted Wistar rats were isolated and perfused either immediately after liver harvesting or after a 24-hr cold (4 degrees C) preservation in University of Wisconsin solution. Hyaluronic acid (150 ng/ml) and taurocholate (11.5 micrograms/ml) were infused into the reservoir, and their eliminations were assessed to evaluate liver endothelial cell function and hepatocyte function, respectively. Liver viability was estimated by intrahepatic resistance, oxygen consumption, bile secretion, and lactate dehydrogenase release. In addition, cell viabilities were evaluated by trypan blue staining. In fed-rat livers, glycogen content did not differ before or after the cold preservation, although a reduction was observed during the subsequent perfusion period. Liver glycogen content in fed rats was markedly higher than in the fasted rats at each time point studied. In fasted and fed rats, liver viability parameters and hepatocyte function were moderately altered, whereas liver endothelial cell function was markedly impaired after cold preservation. However, feeding had no influence on either hepatocyte or liver endothelial cell functions which were similarly altered in both nutritional conditions. The present data show that the nutritional status of liver donors does not play an important role in the preservation of liver endothelial cells after cold ischemia-reperfusion and, thus, should not affect the overall resistance of livers to hypothermic-ischemic injury.
机译:为了验证供体营养状况对冷藏后肝脏保存质量的作用,我们在分离的灌注大鼠肝脏模型中评估了肝细胞和肝内皮细胞的活力和功能。在威斯康星大学溶液中采集肝脏后或在24小时低温(4摄氏度)保存后,立即分离并灌输来自喂食和禁食Wistar大鼠的肝脏。将透明质酸(150 ng / ml)和牛磺胆酸盐(11.5微克/ ml)注入储库中,并评估其清除率,以分别评估肝内皮细胞功能和肝细胞功能。通过肝内抗性,耗氧量,胆汁分泌和乳酸脱氢酶释放来估计肝生存力。另外,通过台盼蓝染色评价细胞活力。在饲喂大鼠肝脏中,尽管在随后的灌注期间观察到糖原含量降低,但在冷藏之前或之后糖原含量没有差异。在研究的每个时间点,喂食大鼠的肝糖原含量均显着高于禁食大鼠。在禁食和进食的大鼠中,肝脏活力参数和肝细胞功能有中等程度的改变,而冷藏后,肝内皮细胞功能明显受损。然而,进食对肝细胞或肝内皮细胞功能均没有影响,而这两种营养条件均发生了类似的变化。目前的数据表明,肝脏供体的营养状况在冷缺血-再灌注后在肝内皮细胞的保存中并不起重要作用,因此,不应影响肝脏对低温缺血性损伤的整体抵抗力。

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