Hepatocyte apoptosis induced by hepatic ischemia-reperfusion injury in cirrhotic rats
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Published on: November 27, 2019
Shao-Qiang Li1, Li-Jian Liang, Jie-Fu Huang
1Departments of Hepatobiliary Surgery, First Affi-liated Hospital, Zhongshan University, Guangzhou 510080, China. lesqch@yahoo.com.cn
Objective:
To investigate whether hepatocyte apoptosis in hepatic ischemia-reperfusion (I/R) injury is mediated by Fas pathway.
Methods:
Fas-mRNA expression detected by in situ hybridization assay, caspase-3 activity measured by fluorescence spectrophotometer, and hepatocyte apoptosis detected by TUNEL assay were compared in different I/R conditions between cirrhotic and normal rats. The relationship was analyzed between hepatocyte apoptosis, Fas-mRNA expression, and caspase-3 activity.
Results:
In cirrhotic rats, Fas-mRNA expression and caspase-3 activity were significantly increased when the ischemic time prolonged, and subsequently, hepatocyte apoptosis was increased (P<0.01). Under the same I/R condition, the Fas-mRNA expression, caspase-3 activity and hepatocyte apoptosis in cirrhotic liver were significantly higher than those in normal liver (P<0.01).
Conclusions:
Hepatocyte apoptosis in hepatic I/R injury might be mediated by Fas pathway. The possible underlying mechanism that cirrhotic liver is more sensitive to ischemic injury than normal liver is alteration of Fas expression level.
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