References
- Aikawa R, Komuro I, Yamazaki T, Zou Y, Kudoh S, Tanaka M, Shiojima I, Hiroi Y, Yazaki Y. Oxidative stress activates extracellular signal-regulated kinases through Src and Ras in cultured cardiac myocytes of neonatal rats. J Clin Invest 100: 1813-1821, 1997 https://doi.org/10.1172/JCI119709
-
Beresewicz A, Maczewski MC, Duda M. Effect of classic preconditioning and diazoxide on endothelial function and
$O_2^-$ and NO generation in the post-ischemic guinea-pig heart. Cardiovas Res 63: 118-129, 2004 https://doi.org/10.1016/j.cardiores.2004.02.012 - Chen EP, Bittner HB, Davis RD, Van Trigt P, Folz RJ. Physiologic effects of extracellular superoxide dismutase transgene overexpression on myocardial function after ischemia and reperfusion injury. J Thorac Cardiovasc Surg 115: 450-458, 1998 https://doi.org/10.1016/S0022-5223(98)70289-2
- Cohen MV, Liu GS, Downey JM. Preconditioning causes improved wall motion as well as smaller infarcts after transient coronary occlusion in rabbits. Circulation 84: 341-349, 1991 https://doi.org/10.1161/01.CIR.84.1.341
- Cuong DV, Kim NR, Joo H, Youm YB, Chung JY, Lee YS, Park WS, Kim EY, Park YS. Subunit composition of ATP-sensitive potassium channels in mitochondria of rat hearts. Mitochondrion 5: 121-133, 2005 https://doi.org/10.1016/j.mito.2004.12.001
- Faraci FM, Didion SP. Vascular protection: superoxide dismutase isoform in the vessel wall. Arterioscler Thromb Vasc Biol 24: 1367-1373, 2004 https://doi.org/10.1161/01.ATV.0000133604.20182.cf
- Dhalla NS, Temsah RM, Nettican T. Role of oxidative stress in cardiovascular diseases. J Hypertens 18: 655-673, 2000 https://doi.org/10.1097/00004872-200018060-00002
- Friedman JS, Lopez MF, Fleming MD, Rivera A, Martin FM, Welsh ML, Boyd A, Doctrow SR, Burakoff SJ. SOD2-deficiency anemia: protein oxidation and altered protein expression reveal targets of damage, stress response, and antioxidant responsiveness. Blood 104: 2565-2573, 2004 https://doi.org/10.1182/blood-2003-11-3858
- Giordano FJ. Oxygen, oxidative stress, hypoxia, and heart failure. J Clin Invest 115: 500-508, 2005 https://doi.org/10.1172/JCI200524408
- Guo ZM, Yang H, Hamilton ML, VanRemmen H, Richardson A. Effects of age and food restriction on oxidative DNA damage and antioxidant enzyme activities in the mouse aorta. Mech of Ageing and Dev 122: 1771-1786, 2001 https://doi.org/10.1016/S0047-6374(01)00298-6
- Hamilton CA, Miller WH, Al-Benna S, Brosnan MJ, Drummond RD, Mcbride MW, Dominiczak AF. Strategies to reduce oxidative stress in cardiovascular disease. Clin Sci 106: 219-234, 2004 https://doi.org/10.1042/CS20030379
- Hanley PJ, Daut J. KATP channels and preconditioning: a re-examination of the role of mitochondrial KATP channels and an overview of alternative mechanisms. J Mol Cell Cardiol 39: 17-50, 2005 https://doi.org/10.1016/j.yjmcc.2005.04.002
- Hinerfeld D, Traini MD, Veinberger RP, Cochran B, Doctrow SR, Harry J, Mellov S. Endogenous mitochondrial oxidative stress: neurodegeneration, proteomic analysis, specific respiratory chain defects, and efficacious antioxidant therapy in superoxide dismutase 2 null mice. J Neurochem 88: 657-667, 2004 https://doi.org/10.1046/j.1471-4159.2003.02195.x
- Hool LC. Reactive oxygen species in cardiac signaling: from mitochondria to plasma membrane ion channel. Clin Exp Pharmacol Physiol 33: 146-151, 2006 https://doi.org/10.1111/j.1440-1681.2006.04341.x
- Jin ZQ, Zhou HZ, Cecchini G, Gray MO, Karliner JS. Mn-SOD in mouse heart: acute responses to ischemic preconditioning and ischemia-reperfusion injury. Am J Physiol Heart Circ Physiol 288: 2986-2994, 2005 https://doi.org/10.1152/ajpheart.01144.2004
- Jolly SR, Kane WJ, Bailie MB, Abrams GD, Lucchesi BR. Canine myocardial reperfusion injury. Its reduction by the combined administration of superoxide and catalase. Circ Res 54: 277- 285, 1984 https://doi.org/10.1161/01.RES.54.3.277
- Kato R, Foex P. Myocardial protection by anesthetic agents against ischemia-reperfusion injury: an update for anesthesiologists. Can J Anesth 49: 777-791, 2002 https://doi.org/10.1007/BF03017409
- Kim HJ, Kim NR, Joo H, Youm JB, Park YS, Warda M, Kang SH, Thu VT, Khoa TM, Jin Han. Differential activation of Ras/Raf/MAPK pathway between heart and cerebral artery in isoproterenol-induced cardiac hypertrophy. Korean J Physiol Pharmacol 9: 299-304, 2005
- Kim NR, Lee YS, Kim HK, Joo H, Youm JB, Park WS, Warda M, Cuong DV, Han J. Potential biomarkers for ischemic heart damage identified in mitochondrial proteins by comparative proteomics. Proteomics 6: 1237-1249, 2006 https://doi.org/10.1002/pmic.200500291
- Kumar D, Lou H, Singal PK. Oxidative stress and apoptosis in heart dysfunction. Herz 27: 662-668, 2002 https://doi.org/10.1007/s00059-002-2430-3
- Li C, Jackson RM. Reactive species mechanisms of cellular hypoxia reoxygenation injury. Am J Physiol Cell Physiol 282: 227-241, 2002 https://doi.org/10.1152/ajpcell.00112.2001
- Li F, Hayes JK, Wong KC. Gene therapy: a novel method for the treatment of myocardial ischemia and reperfusion injury mini review. Stroke 35: 2676-2679, 2004 https://doi.org/10.1161/01.STR.0000143220.21382.fd
-
Liu H, McPherson BC, Yao Z. Preconditioning attenuates apoptosis and necrosis: role of protein kinase C and -
$\gamma$ isoforms. Am J Physiol Heart Circ Physiol 281: 404-410, 2001 https://doi.org/10.1152/ajpheart.2001.281.1.H404 - Lundberg KC, Szweda LI. Preconditioning prevents loss in mitochondrial function and release of cytochrome c during prolonged cardiac ischemia/reperfusion. Arch Biochem Biophys 453: 128-132, 2006
- Maulik N, Yoshida T, Das DK. Oxidative stress developed during the reperfusion of ischemic myocardium induces apoptosis. Free Radic Biol Med 24: 869-875, 1998 https://doi.org/10.1016/S0891-5849(97)00388-2
- Murry CE, Richard VJ, Jennings RB, Reimer KA. Preconditioning with ischemia: a delay of lethal cell injury in ischemic myocardium. Circulation 74: 1124-1136, 1986 https://doi.org/10.1161/01.CIR.74.5.1124
- Murry CE, Richard VJ, Reimer KA, Jennings RB. Ischemic preconditioning slow energy metabolism and delays ultrastructural damage during a sustained ischemic episode. Circ Res 66: 913- 931, 1990 https://doi.org/10.1161/01.RES.66.4.913
- Qian LP, Zhu SS, Cao JL, Zeng YM. Isoflurane preconditioning protects against ischemia-reperfusion injury partly by attenuating cytochrome c release from subsarcolemmal mitochondria in isolated rat hearts. Acta Pharmacol Sin 26: 813-820, 2005 https://doi.org/10.1111/j.1745-7254.2005.00117.x
- Qin F, Shite J, Liang CS. Antioxidants attenuate myocyte apoptosis and improve cardiac function in CHF: association with changes in MAPK pathways. Am J Physiol Heart Circ Physiol 285: 822- 832, 2003 https://doi.org/10.1152/ajpheart.00015.2003
- Shiki K, Hearse DJ. Preconditioning of ischemic myocardium: reperfusion-induced arrhythmias. Am J Physiol 22: 1470-1476, 1987
- Turner NA, Xia F, Azhar G, Zhang X, Liu L, Wei JY. Oxidative stress induces DNA fragmentation and caspase activation via the c-Jun NH2-terminal kinase pathway in H9c2 cardiac muscle cells. J Mol Cell Cardiol 30: 1789-1801, 1998 https://doi.org/10.1006/jmcc.1998.0743
- Wang D, Yang XP, Liu YH, Carretero OA, LaPointe MC. Reduction of myocardial infarct size by inhibition of inducible nitric oxide synthase. Am J Hypertens 12: 174-182, 1999
- Wei YH, Lee HC. Oxidative stress, mitochondrial DNA mutation, and impairment of antioxidant enzymes in aging. Proc Soc Exp Biol Med 217: 53-63, 1998
- Yellon DM, Downey JM. Preconditioning the myocardium: from cellular physiology to clinical cardiology. Physiol Rev 83: 1113- 1151, 2003 https://doi.org/10.1152/physrev.00009.2003
- Zhao Z, Corvera S, Halkos ME, Kerendi F. Inhibition of myocardial injury by ischemic postconditioning during reperfusion: comparison with ischemic preconditioning. Am J Physiol Heart Circ Physiol 285: 579-588, 2003 https://doi.org/10.1152/ajpheart.01064.2002