Korean J Phys Anthropol.
2006 Sep;19(3):165-178.
The Effects of Ischemic Preconditioning and K(ATP) channel Activation on the Expression of the PKC-epsilon, NF-kappaB and AP-1 in Ischemia-reperfused Rat Heart
- Affiliations
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- 1Department of Anatomy and Cell Biology, College of Medicine, Hanyang University, Korea. paikdj@hanyang.ac.kr
- 2Department of Veterinary Medicine, School of Veterinary Medicine, Kwangwon National University, Korea.
- 3Department of Preventive Medicine, College of Medicine, Kangwon National University, Korea.
Abstract
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This study was aimed to elucidate the effects of K(ATP) activation during IPC on the PKC-epsilon, NF-kappaB and AP-1 in
ischemia-reperfused rat hearts. SD male rats weighting from 300 to 350 g were split into 9 groups, such as sham control
(S), IPC, 3 cycles of 5 min ischemia and 5 min reperfusion, continuous preconditioning (CP), 8 cycles of 5 min ischemia
and 5 min reperfusion, K(ATP) opening (KO) with pinacidil (1.0 mg/kg), K(ATP) blocking with glibenclamide (1.0 mg/kg)
injection, ischemia (IS), 30 min ischemia, IPC followed by IS, 8) K(ATP) blocking and IPC followed by IS (KB+IPC+IS),
IS and K(ATP) opening (KO+IS). Heart were subjected to ligation of left descending coronary artery and reperfusion in
groups of IPC, CP, IS with or without IPC. Immunohistochemistry and Western blotting for PKC-epsilon, NF-kappaB and AP-1
were performed at 3, 6, 24 hours after reperfusion or treatment.
Immunoreactivities against PKC-epsilon antibody were observed stronger in the groups of IPC, KO, IPC+IS and KO+IS
than groups of KB, IS and KB+IPC+IS. NF-kappaB activation and translocation were only observed in the groups of
including 30 min ischemia and reperfusion. AP-1 activation and translocation were opposite to the results of PKC-epsilon
activation. In the group of CP, KB, IS and KB+IPC+IS, reactivities of AP-1 antibody were stronger than IPC+IS,
KO+IS, and weaker in the groups of S, IPC and KO.
These results suggest that K(ATP) opening with IPC or pharmacological methods may direct effect on the PKC-epsilon
activation and that K(ATP) blocking has effect on the AP-1 activation and translocation in the heart of ischemiareperfused
of rats.