首页 | 本学科首页   官方微博 | 高级检索  
检索        


Comparison of solutions for preservation of the rabbit liver as tested by isolated perfusion
Authors:G den Butter  A Saunder  D C Marsh  F O Belzer  J H Southard
Institution:(1) Department of Surgery, Clinical Sciences Center, University of Wisconsin, 600 Highland Avenue, 53792 Madison, WI, USA;(2) Present address: Department of Surgery, Diaconessenhuis Eindhoven, Ds. Theodor Fliednerstraat 1, 5631 BM Eindhoven, The Netherlands
Abstract:The University of Wisconsin (UW) solution consists of a relatively complex mixture of agents. In this study we compared simpler preservation solutions, namely, histidine-tryptophan-ketoglutarate glutarate (HTK) and phosphatebuffered sucrose (PBS) with different compositions of UW solution in the isolated perfused rabbit liver model. Livers were stored cold for 24 and 48 h. After 24 h of preservation, the amount of bile produced in UW-preserved livers was significantly greater (P<0.05) than that in HTK-preserved livers. Also, there was less LDH released into the perfusate in UW-preserved livers. There was more edema and lower K+/Na+ rations in HTK-preserved livers than in UW-preserved livers (all data P<0.05). After 48 h of preservation, the differences between livers preserved in UW or HTK solution were less noticeable than at 24 h and bile production was similar. LDH and AST release were greater in HTK-preserved livers than in UW livers, but these differences were not statistically significant. Preservation in PBS for 48 h was worse than in either UW or HTK solution. Substitution of polyethylene glycol (PEG) for hydroxyethyl starch (HES) in 48-h UW-preserved livers was not effective. We conclude that solutions simpler in composition than UW solution may be effective in kidney transplantation but do not appear suitable for successuful liver preservation.
Keywords:Liver preservation  rabbit  Preservation  liver  rabbit  UW solution  HTK solution  liver preservation  HTK solution  UW solution  liver preservation
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号