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首页> 外文期刊>Experimental and clinical transplantation >The Role of Portal Vein Clamping for Cytokine Release and Neutrophils Activity During Liver Resection and Transplant
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The Role of Portal Vein Clamping for Cytokine Release and Neutrophils Activity During Liver Resection and Transplant

机译:肝切除和移植过程中门静脉钳制对细胞因子释放和中性粒细胞活性的作用

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Objectives: Uncontrolled release of cytokines has been linked to graft dysfunction or rejection and contributes to an increase in mortality and morbidity. We argue that temporary vascular clamping of the hepatic pedicle during major hepatic surgery is a potential stimulus for an excessive release of cytokines and the activity of neutrophils. Materials and Methods: Thirty patients underwent partial liver resection or transplant. Samples were drawn preoperatively, immediately before portal vein clamping, at the early reperfusion period, and on days 1, 3, 5, and 7 after the operation. Central venous plasma concentrations of IL-6, IL-8, and TNF-α were compared to portal venous plasma. The influence of neutrophils on metabolic activity was measured by flow cytometry. Results: In both patient groups, no significant differences in cytokine concentrations between central and portal venous plasma were found. However, significant differences of neutrophils activity were observed in patients undergoing partial liver resection compared to patients after transplant. Conclusion: Portal vein stasis induced by clamping the hepatic pedicle has no influence on the local release of IL-6, IL-8, and TNF-α. However, preoperatively increased plasma levels of TNF-α play a decisive role in the metabolic activity of neutrophils in patients with final-stage liver disease.
机译:目的:细胞因子的失控释放与移植物功能障碍或排斥反应有关,并导致死亡率和发病率增加。我们认为,大肝手术期间肝蒂的暂时性血管夹紧是过度释放细胞因子和嗜中性粒细胞活性的潜在刺激。材料和方法:30例患者接受了部分肝切除或移植。术前,门静脉钳夹前,再灌注早期以及术后1、3、5和7天取样。将IL-6,IL-8和TNF-α的中心静脉血浆浓度与门静脉血浆进行比较。中性粒细胞对代谢活性的影响通过流式细胞仪测量。结果:在两个患者组中,未发现中心静脉血和门静脉血血浆中细胞因子浓度的显着差异。但是,与移植后的患者相比,部分肝切除患者的嗜中性粒细胞活性存在显着差异。结论:钳夹肝蒂引起的门静脉淤滞对IL-6,IL-8和TNF-α的局部释放没有影响。然而,术前血浆TNF-α水平的升高对终末期肝病患者中性粒细胞的代谢活性起决定性作用。

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