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肝脏缺血再灌注损伤的生物学调控。

Biological modulation of liver ischemia-reperfusion injury.

机构信息

Department of Visceral and Transplantation Surgery, Swiss HPB and Transplant Center, University Hospital Zurich, Switzerland.

出版信息

Curr Opin Organ Transplant. 2010 Apr;15(2):183-9. doi: 10.1097/MOT.0b013e3283373ced.

Abstract

PURPOSE OF REVIEW

This review gives a broad overview of the key factors of ischemic injury to the liver and presents the current modifications of preservation solutions and the few strategies of biological modulation in clinical use today.

RECENT FINDINGS

Protective effects in human-liver transplantation were shown by methylprednisolone treatment in decreased donors, and by inhalation of a nontoxic dose of nitric oxide in recipients. In addition, recent results showed rescue of pig livers, donated after cardiac death by application of a cocktail of substances addressing several previously identified mechanisms of ischemia-reperfusion injury.

SUMMARY

The future of a pharmacological approach attenuating or preventing ischemia-reperfusion injury lies in a combination of drugs acting simultaneously on several steps of the injury cascades. Applying these substances during flush, before, and during implantation appears as an attractive strategy to protect extended criteria liver grafts.

摘要

目的综述

本文综述了肝脏缺血损伤的关键因素,并介绍了目前保存液的改良和临床应用中少数几种生物学调节策略。

最近的发现

在供体中,甲泼尼龙治疗和在受体中吸入无毒剂量的一氧化氮显示出肝移植中的保护作用。此外,最近的结果表明,通过应用鸡尾酒疗法,可挽救心脏死亡后捐献的猪肝,该疗法针对缺血再灌注损伤的几个先前确定的机制。

总结

减轻或预防缺血再灌注损伤的药物治疗方法的未来在于同时作用于损伤级联的多个步骤的药物的联合应用。在冲洗、植入前和植入过程中应用这些物质似乎是保护扩大标准肝移植物的一种有吸引力的策略。

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