Ischemic preconditioning decreases the reperfusion-related formation of hydroxyl radicals in a rabbit model of regional myocardial ischemia and reperfusion: The role of K_ATP channels

References

• Murry CE, Jennings RB, Reimer KA. Preconditioning with ischemia: A delay of lethal cell injury in ischemic myocardium. Circulation 1986;74:1124–1136.
   Google Scholar
• Li YW, Whittaker P, Kloner RA. The transient nature of the effect of ischemic preconditioning on myocardial infarct size and ventricular arrhythmia. Am Heart J 1992;123:346–353.
   Google Scholar
• Alkhulaifi AM. Preconditioning the human heart. Ann R Coll Surg Engl 1997;79:49–54.
   PubMed Web of Science ®Google Scholar
• Kloner RA, Jennings RB. Consequences of brief ischemia: Stunning, preconditioning, and their clinical implications: Part 1. Circulation 2001;104:2981–2989.
   PubMed Web of Science ®Google Scholar
• Jennings RB, Murry C, Reimer KA. Myocardial effects of brief periods of ischemia followed by reperfusion. Adv Cardiol 1990;37:7–31.
   Google Scholar
• Piper HM, Meuter K, Schafer C. Cellular mechanisms of ischemia-reperfusion injury. Ann Thorac Surg 2003;-75:-S644—S648.
   Google Scholar
• Bolli R. Mechanism of myocardial "stunning". Circulation 1990;82:723–738.
   PubMed Web of Science ®Google Scholar
• Ferrari R, Ceconi C, Curello S, Percoco G, Toselli T, Antonioli G. Ischemic preconditioning, myocardial stunning, and hibernation: Basic aspects. Am Heart J 1999;138:561–568.
   Web of Science ®Google Scholar
• Becker LC, Ambrosio G. Myocardial consequences of reperfusion. Prog Cardiovasc Dis 1987;30:23–44.
   PubMed Web of Science ®Google Scholar
• Becker LB, Vanden Hoek TL, Shao ZH, Li CQ, Schumacker PT. Generation of superoxide in cardiomyocytes during ischemia before reperfusion. Am J Physiol 1999;277:H2240—H2246.
   Google Scholar
• Schulz R, Cohen MV, Behrends M, Downey JM, Heusch G. Signal transduction of ischemic preconditioning. Cardiovasc Res 2001;52:181–198.
   Google Scholar
• Vanden Hoek T, Becker LB, Shao ZH, Li CQ, Schumacker PT. Preconditioning in cardiomyocytes protects by attenuating oxidant stress at reperfusion. Circ Res 2000;86:541–548.
   Google Scholar
• Zhai X, Zhou X, Ashraf M. Late ischemic preconditioning is mediated in myocytes by enhanced endogenous antioxidant activity stimulated by oxygen-derived free radicals. Ann N Y Acad Sci 1996;793:156–166.
   Google Scholar
• Zhou X, Zhai X, Ashraf M. Direct evidence that initial oxidative stress triggered by preconditioning contributes to second window of protection by endogenous antioxidant enzyme in myocytes. Circulation 1996;93:1177–1184.
   Google Scholar
• Chen W, Gabel S, Steenbergen C, Murphy E. A redox-based mechanism for cardioprotection induced by ischemic pre-conditioning in perfused rat heart. Circ Res 1995;77:424–429.
   PubMed Web of Science ®Google Scholar
• Baines CP, Goto M, Downey JM. Oxygen radicals released during ischemic preconditioning contribute to cardioprotec-tion in the rabbit myocardium. J Mol Cell Cardiol 1997;29:207–216.
   Google Scholar
• Myers ML, Bolli R, Lekich RF, Hartley CJ, Roberts R. Enhancement of recovery of myocardial function by oxygen free-radical scavengers after reversible regional ischemia. Circulation 1985;72:915–921.
   Google Scholar
• Powell SR, Hall D. Use of salicylate as a probe for •OH formation in isolated ischemic rat hearts. Free Radic Biol Med 1990;9:133–141.
   PubMed Web of Science ®Google Scholar
• Gross GJ. The role of mitochondrial KATI. channels in cardioprotection. Basic Res Cardiol 2000;95:280–284.
   PubMedGoogle Scholar
• Kersten JR, Gross GJ, Pagel PS, Warltier DC. Activation of adenosine triphosphate-regulated potassium channels: Mediation of cellular and organ protection. Anesthesiology 1998;88:495–513.
   PubMed Web of Science ®Google Scholar
• Gross GJ, Fryer RM. Mitochondrial K(ATP) channels: Triggers or distal effectors of ischemic or pharmacological preconditioning? Circ Res 2000;87:431–433.
   PubMed Web of Science ®Google Scholar
• Yue Y, Qin Q, Cohen MV, Downey JM, Critz SD. The relative order of mK(ATp) channels, free radicals and p38 MAPK in preconditioning's protective pathway in rat heart. Cardiovasc Res 2002;55: 681–689.
   Google Scholar
• Onodera T, Ashraf M. Detection of hydroxyl radicals in the postischemic reperfused heart using salicylate as a trapping agent. J Mol Cell Cardiol 1991;23:365–370.
   PubMed Web of Science ®Google Scholar
• Kevin LG, Camara AK, Riess ML, Novalija E, Stowe DF. Ischemic preconditioning alters real-time measure of 02 radicals in intact hearts with ischemia and reperfusion. Am J Physiol Heart Circ Physiol 2003;284:H566–H574.
   Google Scholar
• Glantz L, Ginosar Y, Chevion M, Gozal Y, Elami A, Navot N, Kitrossky N, Drenger B. Halothane prevents postischemic production of hydroxyl radicals in the canine heart. Anesthesiology 1997;86:440–447.
   PubMed Web of Science ®Google Scholar
• Granville DJ, Tashakkor B, Takeuchi C, Gustafsson AB, Huang C, Sayen MR, Wentworth Jr., P, Yeager M, Gottlieb RA. Reduction of ischemia and reperfusion induced myo-cardial damage by cytochrome P450 inhibitors. Proc Natl Acad Sci USA 2004;191: 1321–1326.
   Google Scholar
• Oldenburg 0, Yang X1\4, Krieg T, Garlid KD, Cohen MV, Grover GJ, Downey JM. P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts. J Mol Cell Cardiol 2003;35: 1035–1042.
   Google Scholar
• McCully JD, Levitsky S. The mitochondrial K(ATP) channel and cardioprotection. Ann Thorac Surg 2003;75:5667–5673.
   Web of Science ®Google Scholar
• Belles B, Hescheler J, Trube G. Changes of membrane currents in cardiac cells induced by long whole-cell recordings and tolbutamide. Pflugers Arch 1987;409:582–588.
   Google Scholar
• Fosset M, De Weille JR, Green RD, Schmid-Antomarchi H, Lazdunski M. Antidiabetic sulfonylureas control action potential properties in heart cells via high affinity receptors that are linked to ATP-dependent K+ channels. J Biol Chem 1988;263:7933–7936.
   Google Scholar
• Jaburek M, Yarov-Yarovoy V, Paucek P, Garlid KD. State-dependent inhibition of the mitochondrial KATI, channel by glyburide and 5-hydroxydecanoate. J Biol Chem 1998;273:13578–13582.
   PubMed Web of Science ®Google Scholar
• Jung 0, Englert HC, Jung W, Gogelein H, Scholkens BA, Busch AE, Linz W. The KATI, channel blocker HMR 1883 does not abolish the benefit of ischemic preconditioning on myocardial infarct mass in anesthetized rabbits. Naunyn Schmiedebergs Arch Pharmacol 2000;361: 445–451.
   Google Scholar
• Sanada S, Kitakaze M, Asanuma H, Harada K, Ogita H, Node K, Takashima S, Sakata Y, Asakura M, Shinozaki Y, Mori H, Kuzuya T, Hon i M. Role of mitochondrial and sarcolemmal KATp channels in ischemic preconditioning of the canine heart. Am J Physiol Heart Circ Physiol 2001;280:H256–H263.
   Google Scholar
• Pain T, Yang XI\4, Critz SD, Yue Y, Nakano A, Liu GS, Heusch G, Cohen MV, Downey JM. Opening of mitochon-drial KATp channels triggers the preconditioned state by generating free radicals. Circ Res 2000;87:460–466.
   Google Scholar
• Bhatnagar A, Srivastava SK, Szabo G. Oxidative stress alters specific membrane currents in isolated cardiac myocytes. Circ Res 1990;67:535–549.
   Google Scholar
• Jahr RI, Cole WC. Alterations in electrical activity and membrane currents induced by intracellular oxygen-derived free radical stress in guinea pig ventricular myocytes. Circ Res 1993;72:1229–1244.
   PubMed Web of Science ®Google Scholar
• Uraizee A, Reimer KA, Murry CE, Jennings RB. Failure of superoxide dismutase to limit size of myocardial infarction after 40 min of ischemia and 4 days of reperfusion in dogs. Circulation 1987;75:1237–1248.
   PubMed Web of Science ®Google Scholar
• Gallagher KP, Buda AJ, Pace D, Gerren RA, Shlafer M. Failure of superoxide dismutase and catalase to alter size of infarction in conscious dogs after 3 hours of occlusion followed by reperfusion. Circulation 1986;73: 1065–1076.
   Google Scholar
• Crestanello JA, Lingle DM, Kamelgard J, Millili J, Whitman GJ. Ischemic preconditioning decreases oxidative stress during reperfusion: A chemiluminescence studies. J Surg Res 1996;65:53–58.
   Google Scholar
• Li Q, Bolli R, Qiu Y, Tang XL, Guo Y, French BA. Gene therapy with extracellular superoxide dismutase protects conscious rabbits against myocardial infarction. Circulation 2001;103:1893–1898.
   PubMed Web of Science ®Google Scholar
• Maxwell MP, Hearse DJ, Yellon DM. Species variation in the coronary collateral circulation during regional myocardial ischaemia: A critical determinant of the rate of evolution and extent of myocardial infarction. Cardiovasc Res 1987;21:737–746.
   Google Scholar
• Hale SL, Kloner RA. Location as a determinant of myocardial infarction in rabbits. J Mol Cell Cardiol 2000;32:505–510.
   PubMed Web of Science ®Google Scholar