Effects of gentle liver manipulation in vivo on hepatic ischemia-reperfusion injury in rats and its mechanism
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Effects of gentle liver manipulation in vivo on hepatic ischemia-reperfusion injury in rats and its mechanism
Journal of Chongqing Medical UniversityVol. 38, Issue 4, Pages: 569-572(2014)
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郑州大学第二附属医院普外科,郑州,450004
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Published:2014,
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Li Shengwei, Liu Chao, Pang Zhigang, et al. Effects of gentle liver manipulation in vivo on hepatic ischemia-reperfusion injury in rats and its mechanism. [J]. Journal of Chongqing Medical University 38(4):569-572(2014)
DOI:
Li Shengwei, Liu Chao, Pang Zhigang, et al. Effects of gentle liver manipulation in vivo on hepatic ischemia-reperfusion injury in rats and its mechanism. [J]. Journal of Chongqing Medical University 38(4):569-572(2014)DOI:
Effects of gentle liver manipulation in vivo on hepatic ischemia-reperfusion injury in rats and its mechanism
Objective:To investigate the effects of the gentle liver manipulation,including toching,retracting and moving liver lobes gently,on hepatic ischemia-reperfusion injury during hepatic ischemia and its mechanism. Methods:Thirty SD rats were divided into three groups randomly:sham-operated group(sham group),ischemia reperfusion group(IR group:produced by total inflow occlusion for 15 min) and manipulation group(MN group:induced with 13 min gentle manipulation including touching,retracting and moving lobes during 15 min ischemia). Serum aminotransferases alanine transaminase and aspartate aminotransferase(ALT and AST),tumor necrosis factor-α(TNF-α) and Pselection in the liver were measured after reperfusion. Results:In MN and IR groups,serum ALT and AST(P=0.000) as well as pathological injury scores(P=0.000) were increased;TNF-α and P-selection expressions were higher(P=0.000) compared with those in sham group. Those variables mentioned above were significantly increased in MN group compared with those in IR group(P=0.000). Conclusions:Gentle in vivo liver manipulation increases the reperfusion injury during hepatic is-chemia,which may be caused by the decrease of pro-inflammatory and activity of neutophils.
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