Liver Graft Exposure to Carbon Monoxide During Cold Storage Protects Sinusoidal Endothelial Cells and Ameliorates Reperfusion Injury in Rats

被引:39
作者
Ikeda, Atsushi [1 ]
Ueki, Shinya [1 ]
Nakao, Atsunori [1 ]
Tomiyama, Koji [1 ]
Ross, Mark A. [2 ]
Stolz, Donna B. [2 ]
Geller, David A. [1 ]
Murase, Noriko [1 ]
机构
[1] Univ Pittsburgh, Dept Surg, Thomas E Starzl Transplantat Inst, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Ctr Biol Imaging, Pittsburgh, PA 15213 USA
基金
美国国家卫生研究院;
关键词
HEPATIC ISCHEMIA/REPERFUSION INJURY; ICAM-1; EXPRESSION; ISCHEMIC-INJURY; HEME OXYGENASE; NITRIC-OXIDE; PRESERVATION; ACTIVATION; APOPTOSIS; DAMAGE; MODULATION;
D O I
10.1002/lt.21918
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatic ischemia/reperfusion (I/R) injury significantly influences short-term and long-term outcomes after liver transplantation (LTx). The critical step initiating the injury is known to include sinusoidal endothelial cell (SEC) alteration during the cold preservation period. As carbon monoxide (CO) has potent cytoprotective functions on vascular endothelial cells, this study examined if CO treatment of excised liver grafts during cold storage could protect SECs and ameliorate hepatic I/R injury. Rat liver grafts were preserved in University of Wisconsin (UW) solution containing 5% CO (CO-UW solution) for 18 to 24 hours and were transplanted into syngeneic Lewis rats. After 18 hours of cold preservation, SEC damage was evident with propidium iodide (PI) nuclear staining on SECs, and the frequency of PI+ SECs was significantly lower in grafts stored in CO-UW solution versus those stored in control UW solution. SEC protection with CO was associated with decreased intercellular cell adhesion molecule translocation and less matrix metalloproteinase release during cold preservation. After LTx with 18 hours of cold preservation, serum alanine aminotransferase levels and hepatic necrosis were significantly less in the CO-UW group than in the control UW group. With 24 hours of cold storage, 35% (7/20) survived with control UW solution, whereas the survival with CO-UW solution improved to 80% (8/10). These beneficial effects of CO-UW solution were associated with a significant reduction of neutrophil extravasation, down-regulation of hepatic messenger RNA for tumor necrosis factor alpha and intercellular cell adhesion molecule 1, and less hepatic extracellular signal-regulated kinase activation. Liver grafts from Kupffer cell-depleted donors or pseudogerm-free donors showed less SEC death during cold preservation, and CO-UW solution further reduced SEC death. In conclusion, CO delivery to excised liver grafts during cold preservation efficiently ameliorates SEC damage and hepatic I/R injury. Liver Transpl 15:1458-1468, 2009. (C) 2009 AASLD.
引用
收藏
页码:1458 / 1468
页数:11
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