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KMID : 0855520070200010045
Korean Journal of Physical Anthropology
2007 Volume.20 No. 1 p.45 ~ p.57
Expressions of the Proinflammatory Cytokines in Rat Kidney with Cyclic Episodes of Short Ischemia-reperfusion of Left Common Iliac Artery
Park Hyun-Joo

Kim Won-Kyu
Youn Jee-Hee
Paik Doo-Jin
Abstract
The purpose of this study is to investigate the changes in NF-¥êB and proinflammatory cytokines expression following courses of reperfusion after various cycles of ischemic preconditioning in the rat kidney.
Thirty five weeks old Sprague Dawley rats were subjected to 3, 6 and 10 cycles of ischemic preconditioning that composed of 5 min ischemia and 5 min reperfusion at the left common iliac artery using rodent vascular clamp. The left kidney obtained after 0, 3, 6, 24 and 72 hours of reperfusion followed by each cycle. The expression patterns of NF-¥êB, TNF-¥á, IL-1¥â and ICAM-1 were detected by immunohistochemical staining and Western blotting methods. Apoptosis were detected by TUNEL assay.
The results were as follows;
In the ischemic preconditioning group, the mortality increased from 24 hours after reperfusion when cyclic episodes of short ischemia and reperfusion were increased. The highest level of NF-¥êB expression in outer medulla of the kidney from 0 hr to 24 hrs of reperfusion is detected after 10 cycles of ischemic preconditioning. The highest level of NF-¥êB expression at 72 hrs of reperfusion is revealed after 3 cycles of ischemic preconditioning. The highest level of TNF-¥á expression in outer medulla of the kidney at 0 hr and 6, 24, 72hrs of reperfusion is shown after 10 cycles of ischemic preconditioning. After 3 hrs of reperfusion, all ischemic preconditioning groups shows similar expression. The highest level of IL-1¥â and ICAM-1 expression in outer medulla of the kidney is observed at all of reperfusion times after 10 cycles of ischemic preconditioning. The highest level of apoptosis in rat kidney outer medulla at all of reperfusion times is shown after 10 cycles of ischemic preconditioning.
In conclusion, 3 or 6 times of remote ischemic preconditioning in the common iliac artery could reduce the expression of NF-¥êB, TNF-¥á, IL-1¥â, and ICAM-1. However, more than 10 times of remote ischemic preconditioning increased ischemia-reperfusion injury, caused by increased expression of NF-¥êB, TNF-¥á, IL-1¥â, and ICAM-1.
KEYWORD
proinflammatory cytokine, TNF-¥á, IL-1¥â, NF-¥êB, ICAM-1, Short ischemia and reperfusion, Ischemic preconditioning, Kidney, Proinflammatory cytokine
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