Heme oxygenase-1 overexpression protects rat livers from ischemia/reperfusion injury with extended cold preservation

被引:155
作者
Kato, H
Amersi, F
Buelow, R
Melinek, J
Coito, AJ
Ke, B
Busuttil, RW
Kupiec-Weglinski, JW [1 ]
机构
[1] Univ Calif Los Angeles, Dumont UCLA Transplant Ctr, Div Liver & Pancreas Transplantat, Dept Surg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[3] SangStat Med Corp, Fremont, CA 94555 USA
关键词
heme oxygenase; ischemia/reperfusion injury; liver;
D O I
10.1034/j.1600-6143.2001.001002121.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
This study analyzes the effects and mechanisms of heme oxygenase-1 (HO-1)-mediated cytoprotection in rat livers exposed to cold preservation. In the first series, rats were pretreated with cobalt protoporphyrin (CoPP) or zinc protoporphyrin (ZnPP), HO-1 inducer and antagonist, respectively. Livers were stored at 4degreesC for 24h, and then perfused ex vivo for 2h. Livers pretreated with CoPP had significantly higher portal venous blood flow and increased total bile production, as compared with the ZnPP group. This correlated with histologic (Banff) criteria of hepatocyte injury/liver function. In the second series, rat livers were stored at 4degreesC for 24 h or 40 h, and then transplanted into syngeneic recipients. After 24h of preservation, 80% of rats bearing CoPP-pretreated liver grafts survived 21 days (vs. 50% in controls). After 40h of cold preservation, liver transplant survival at day 1, 7 and 21 for the CoPP group was: 100%, 71% and 57%, respectively (vs. 50%, 50% and 33% in controls). This correlated with Improved hepatic function/histologic (Suzuki) criteria of hepatocyte injury after HO-1 overexpression (immunohistology/Western blots) by infiltrating macrophages. This study documents the potential utility of HO-1-inducing agents In preventing ischemia/reperfusion injury resulting from prolonged storage of liver transplants.
引用
收藏
页码:121 / 128
页数:8
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