ATP-sensitive K+ channels are not involved in ischemia-reperfusion lung endothelial injury
1995
Khimenko, Pavel L., Timothy M. Moore, and Aubrey E. Taylor. ATP-sensitive K + channels are not involved in ischemia-reperfusion lung endothelial injury. J. Appl. Phy.siol. 79(2) : 554-559, 1995.-The role of ATP-sensitive K + channels (K ATP ) in ischemia and reperfusion (I/R) was studied in isolated rat lungs. I/R produced a sixfold increase in endothelial permeability as measured by the capillary filtration coefficient. Cromakalim (10 μM) given at 46 min after reperfusion reversed the filtration coefficient increase. This effect was not blocked by either a protein kinase A inhibitor (adenosine-3',5'-cyclic monophosphothioate ; 100 μM) or an adenosine antagonist [8-(p-sulfophenyl)-theophylline ; 20 μM]. Cromakalim given before ischemia or at the beginning of reperfusion protected the endothelial barrier from injury. Glibenclamide (500 μM) given before the ischemic period, at the beginning of reperfusion, or 46 min after reperfusion did not alter the changes in microvascular permeability produced by I/R. Glibenclamide blocked the ability of cromakalim to reverse endothelial damage but not the ability of either isoproterenol (10 μM) or an adenosine A 2 -receptor agonist, CGS-21680 (300 nM). We conclude that opening of K ATP channels does not produce endothelial injury in I/R. The activation of K ATp channels can both protect against and reverse the endothelial damage associated with I/R. This novel mechanism(s) is independent from known pathways that employ CAMP-protein kinase system and adenosine.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
0
References
13
Citations
NaN
KQI