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KMID : 0191120110260020290
Journal of Korean Medical Science
2011 Volume.26 No. 2 p.290 ~ p.296
Morphine Postconditioning Attenuates ICAM-1 Expression on Endothelial Cells
Min Too-Jae

Kim Joong-Il
Kim Jae-Hwan
Noh Kyung-Hee
Kim Tae-Woo
Kim Woon-Young
Lee Yoon-Sook
Park Young-Cheol
Abstract
The purpose of this study is to determine 1) whether morphine postconditiong (MPostC) can attenuate the intercellular adhesion molecules-1 (ICAM-1) expression after reoxygenation injury and 2) the subtype(s) of the opioid receptors (ORs) that are involved with MPostC. Human umbilical vein endothelial cells (HUVECs) were subjected to 6 hr anoxia followed by 12 hr reoxygenation. Three morphine concentrations (0.3, 3, 30 ¥ìM) were used to evaluate the protective effect of MPostC. We also investigated blockading the OR subtypes¡¯ effects on MPostC by using three antagonists (a ¥ì-OR antagonist naloxone, a ¥ê-OR antagonist nor-binaltorphimine, and a ¥ä-OR antagonist naltrindole) and the inhibitor of protein kinase C (PKC) chelerythrine. As results, the ICAM-1 expression was significantly reduced in the MPostC (3, 30 ¥ìM) groups compared to the control group at 1, 6, 9, and 12 hours reoxygenation time. As a consequence, neutrophil adhesion was also decreased after MPostC. These effects were abolished by coadministering chelerythrine, nor-binaltorphimine or naltrindole, but not with naloxone. In conclusion, it is assumed that MPostC could attenuate the expression of ICAM-1 on endothelial cells during reoxygenation via the ¥ê and ¥ä-OR (opioid receptor)-specific pathway, and this also involves a PKC-dependent pathway.
KEYWORD
Morphine, Postconditioning, Reperfusion injury, Humans, Umblical Veins, Endothelial Cells, Cell Culture
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