目的 探討缺血預(yù)處理(ischemic preconditioning,IP)對(duì)大鼠移植肝臟缺血再灌注損傷的保護(hù)作用。方法采用SD大鼠原位肝移植動(dòng)物模型,供肝冷保存時(shí)間100 min,無(wú)肝期25 min。64只SD大鼠隨機(jī)均分成兩組: 對(duì)照組,獲取供肝前僅以肝素生理鹽水經(jīng)門(mén)靜脈灌注; IP組,獲取供肝前阻斷肝門(mén)血供10 min,再灌注10 min,然后再以肝素生理鹽水經(jīng)門(mén)靜脈灌注。每組受體的一半(n=8)用于觀(guān)察存活率,另一半(n=8)用于移植肝臟再灌注2 h后取血及肝臟檢測(cè)。結(jié)果IP組的1 w存活率、膽汁分泌量、抗氧化酶活力、血清NO水平均明顯高于對(duì)照組(P<0.05),血清ALT、AST、LDH、TNF及肝組織中的過(guò)氧化產(chǎn)物含量均明顯低于對(duì)照組(P<0.05),組織的病理改變也輕于對(duì)照組。結(jié)論IP能夠提高血清NO水平,降低血清TNF含量,對(duì)大鼠移植肝臟的缺血再灌注損傷具有保護(hù)作用。
引用本文: 涂兵,嚴(yán)律南,劉智敏. 缺血預(yù)處理對(duì)大鼠移植肝臟缺血再灌注損傷的保護(hù)作用. 中國(guó)普外基礎(chǔ)與臨床雜志, 2002, 9(2): 89-92. doi: 復(fù)制
1. | Lemasters JJ,Bunzendahl H,Thurman RG.Reperfusion injury to donor livers stored for transplantation.Liver \[J\].Transplant Surg,1995; 1(2)∶124. |
2. | Bilzer M, Gerbs AL.Preservation injury of the liver:mechanism and novel therapeutic strategies \[J\].J Hepatol,2000; 32(3)∶508. |
3. | Kamada N,Calne RY. A surgical experience with five hundred thirty liver transplants in the rat \[J\].Surgery,1983; 93(1 Pt 1)∶64. |
4. | Ploeg RJ,D’Alessandro AM,Knechtle SJ,et al.Risk factors for primary dysfunction after liver transplantation:a multivariate analysis \[J\].Transplantation,1993; 55(4)∶807. |
5. | Jaeschke H.Preservation injury:mechanisms,prevention and consequences \[J\].J Hepatol, 1996; 25(5)∶774. |
6. | Murry CE,Jennings RB,Reimer KA.Preconditioning with ischemia: a delay of lethal cell injury in ischemic myocardium \[J\].Circulation,1986; 74(5)∶1124. |
7. | Lichtman SN,Lemasters JJ.Role of cytokines and cytokineproducing cells in reperfusion injury to the liver.Semin \[J\].Liver Dis,1999; 19(2)∶171. |
8. | Shibuya H,Ohkohchi N,Tsukamoto S,et al.Tumor necrosis factorinduced superoxidemediated neutrophil accumulation in cold ischemic/reperfused rat liver \[J\].Hepatology,1997; 26(1)∶113. |
9. | Nishida T,Gatmaitan Z,Che MX,et al.Rat liver canalicular membrane vesicles contain an ATPdependent bile acid transport system \[J\].Proc Natl Acad Sci USA,1991; 88(15)∶6590. |
10. | Bautista AP,Spitzer JJ. Inhibition of nitric oxide formation in vivo enhances superoxide release by the perfused liver \[J\].Am J Physiol,1994; 266(5 Pt 1)∶G783. |
- 1. Lemasters JJ,Bunzendahl H,Thurman RG.Reperfusion injury to donor livers stored for transplantation.Liver \[J\].Transplant Surg,1995; 1(2)∶124.
- 2. Bilzer M, Gerbs AL.Preservation injury of the liver:mechanism and novel therapeutic strategies \[J\].J Hepatol,2000; 32(3)∶508.
- 3. Kamada N,Calne RY. A surgical experience with five hundred thirty liver transplants in the rat \[J\].Surgery,1983; 93(1 Pt 1)∶64.
- 4. Ploeg RJ,D’Alessandro AM,Knechtle SJ,et al.Risk factors for primary dysfunction after liver transplantation:a multivariate analysis \[J\].Transplantation,1993; 55(4)∶807.
- 5. Jaeschke H.Preservation injury:mechanisms,prevention and consequences \[J\].J Hepatol, 1996; 25(5)∶774.
- 6. Murry CE,Jennings RB,Reimer KA.Preconditioning with ischemia: a delay of lethal cell injury in ischemic myocardium \[J\].Circulation,1986; 74(5)∶1124.
- 7. Lichtman SN,Lemasters JJ.Role of cytokines and cytokineproducing cells in reperfusion injury to the liver.Semin \[J\].Liver Dis,1999; 19(2)∶171.
- 8. Shibuya H,Ohkohchi N,Tsukamoto S,et al.Tumor necrosis factorinduced superoxidemediated neutrophil accumulation in cold ischemic/reperfused rat liver \[J\].Hepatology,1997; 26(1)∶113.
- 9. Nishida T,Gatmaitan Z,Che MX,et al.Rat liver canalicular membrane vesicles contain an ATPdependent bile acid transport system \[J\].Proc Natl Acad Sci USA,1991; 88(15)∶6590.
- 10. Bautista AP,Spitzer JJ. Inhibition of nitric oxide formation in vivo enhances superoxide release by the perfused liver \[J\].Am J Physiol,1994; 266(5 Pt 1)∶G783.