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肠保护的器官特异性解决方案和策略

Organ-specific solutions and strategies for the intestinal preservation.

机构信息

1The Transplant Institute, Sahlgrenska University Hospital , Gothenburg , Sweden.

出版信息

Int Rev Immunol. 2014 May-Jun;33(3):234-44. doi: 10.3109/08830185.2013.853764. Epub 2013 Dec 12.

Abstract

Among the intraabdominal organs, the intestine is the most susceptible to storage injury and as a consequence its safe cold ischemic time in the clinic is restricted to below 10 hours. The current practice for the intestinal preservation (IP) consists of an in-situ vascular flush with iced University of Wisconsin or Histidine-Tryptophan-Ketoglutarate solution followed by cold storage at 4°C. Mucosal injury is initiated within 1 hour and rapidly progresses to mucosal breakdown; tissue injury worsens upon reperfusion and further impairs the mucosal barrier, favoring bacterial translocation and sepsis. In addition of releasing danger signals, an advanced ischemia-reperfusion injury (IRI) may increase graft immunogenicity and promote rejection. Several alternative approaches have been tested as alternatives to the static storage. The aim of this review is to summarize and discuss the various intraluminal interventions as additional strategies aiming to reduce the IP/reperfusion injury and highlight the underlying pathophysiological mechanisms.

摘要

在腹腔内器官中,肠最容易发生储存损伤,因此其在临床上安全的冷缺血时间限制在 10 小时以下。目前的肠道保存(IP)实践包括用冰 UW 或组氨酸-色氨酸-酮戊二酸溶液进行原位血管冲洗,然后在 4°C 下冷藏。黏膜损伤在 1 小时内开始,并迅速进展为黏膜破裂;再灌注后组织损伤加重,进一步损害黏膜屏障,有利于细菌易位和脓毒症。除了释放危险信号外,先进的缺血再灌注损伤(IRI)可能会增加移植物的免疫原性并促进排斥反应。已经测试了几种替代方法作为静态存储的替代品。本文的目的是总结和讨论各种腔内干预措施作为额外的策略,旨在减少 IP/再灌注损伤,并强调潜在的病理生理机制。

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