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一种用于离体大鼠肝脏无血红蛋白灌注的改进系统。

An improved system for hemoglobin-free perfusion of isolated rat livers.

作者信息

Schmucker D L, Jones A L, Michielsen C E

出版信息

Lab Invest. 1975 Aug;33(2):168-75.

PMID:1160341
Abstract

Fine structure and several parameters of hepatic function were evaluated in isolated rat livers perfused with a hemoglobin-free medium in a newly designed organ perfusion system. The preservation of hepatic fine structure and the maintenance of certain functional criteria, including oxygen consumption, bile secretion rate, and the retention of intracellular potassium ions, demonstrated that these livers had been successfully perfused for up to 5 hours. The medium contained neither red blood cells nor other oxygen carriers, such as fluorocarbon emulsions. The use of hyperbaric oxygenation eliminates the requirement for hemoglobin in the perfusion medium. In addition, the extensive endothelial cell injury associated with the use of hemoglobin-free media is avoided since this system permits perfusion at near physiologic hepatic portal vein flow rates. The quality of isolated livers perfused without albumin in medium suggests that an oncotic agent is not required for rat liver perfusion.

摘要

在一个新设计的器官灌注系统中,使用无血红蛋白的培养基灌注分离的大鼠肝脏,对肝脏的精细结构和几个肝功能参数进行了评估。肝脏精细结构的保存以及某些功能指标的维持,包括耗氧量、胆汁分泌率和细胞内钾离子的保留,表明这些肝脏已成功灌注长达5小时。该培养基既不包含红细胞也不包含其他氧载体,如氟碳乳液。高压氧合的使用消除了灌注培养基中对血红蛋白的需求。此外,由于该系统允许以接近生理的肝门静脉流速进行灌注,避免了与使用无血红蛋白培养基相关的广泛内皮细胞损伤。在无白蛋白的培养基中灌注分离肝脏的质量表明,大鼠肝脏灌注不需要渗透剂。

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