TY - JOUR
T1 - Ischemic preconditioning in hepatic ischemic–reperfusion injury
AU - Kuo, Sheng Chih
AU - Liu, Yueh Wei
AU - Tsai, Ching Hua
AU - Sheen-Chen, Shyr Ming
N1 - Publisher Copyright:
© 2016
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Background/Introduction Ischemic preconditioning is a method in which brief periods of ischemia render tissues resistant to injury resulting from prolonged ischemia and reperfusion, so-called ischemia–reperfusion injury. Purpose To elucidate the possible protective role of ischemic preconditioning in rat livers with ischemia–reperfusion injury. Methods Rats were first allocated to either a sham control or an ischemic preconditioning group. On the following day, the rats from each group were administered either 30 minutes or 45 minutes hepatic ischemia. Next, rat livers were harvested for measuring proliferating cell nuclear antigen, heme oxygenase-1, inducible nitric oxide synthase, and heat shock protein 70 mRNA levels. Results Both proliferating cell nuclear antigen and hemeoxygenase-1 expression increased significantly after 45 minutes hepatic ischemia compared with those after 30 minutes hepatic ischemia, but they decreased significantly with ischemic preconditioning. However, ischemic preconditioning did not affect inducible nitric oxide synthase or heat shock protein 70 expression. Conclusion From the preliminary findings, further elucidation is warranted.
AB - Background/Introduction Ischemic preconditioning is a method in which brief periods of ischemia render tissues resistant to injury resulting from prolonged ischemia and reperfusion, so-called ischemia–reperfusion injury. Purpose To elucidate the possible protective role of ischemic preconditioning in rat livers with ischemia–reperfusion injury. Methods Rats were first allocated to either a sham control or an ischemic preconditioning group. On the following day, the rats from each group were administered either 30 minutes or 45 minutes hepatic ischemia. Next, rat livers were harvested for measuring proliferating cell nuclear antigen, heme oxygenase-1, inducible nitric oxide synthase, and heat shock protein 70 mRNA levels. Results Both proliferating cell nuclear antigen and hemeoxygenase-1 expression increased significantly after 45 minutes hepatic ischemia compared with those after 30 minutes hepatic ischemia, but they decreased significantly with ischemic preconditioning. However, ischemic preconditioning did not affect inducible nitric oxide synthase or heat shock protein 70 expression. Conclusion From the preliminary findings, further elucidation is warranted.
KW - ischemia–reperfusion injury
KW - liver
KW - preconditioning
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U2 - 10.1016/j.fjs.2016.03.003
DO - 10.1016/j.fjs.2016.03.003
M3 - Article
AN - SCOPUS:84992409164
SN - 1682-606X
VL - 49
SP - 169
EP - 173
JO - Formosan Journal of Surgery
JF - Formosan Journal of Surgery
IS - 5
ER -