Reactive oxygen species released from mitochondria during brief hypoxia induce preconditioning in cardiomyocytes
Open accessAbstract
Reactive oxygen species (ROS) have been proposed to participate in the induction of cardiac preconditioning. However, their source and mechanism of induction are unclear. We tested whether brief hypoxia induces preconditioning by augmenting mitochondrial generation of ROS in chick cardiomyocytes. Cells were preconditioned with 10 min of hypoxia, followed by 1 h of simulated ischemia and 3 h of reperfusion. Preconditioning decreased cell death from 47 +/- 3% to 14 +/- 2%. Return of contraction was observed in 3/3 preconditioned versus 0/6 non-preconditioned experiments. During induction, ROS oxidation of the probe dichlorofluorescin (sensitive to H2O2) increased approximately 2.5-fold. As a substitute for hypoxia, the addition of H2O2 (15 micromol/liter) during normoxia also induced preconditioning-like protection. Conversely, the ROS signal during hypoxia was attenuated with the thiol reductant 2-mercaptopropionyl glycine, the cytosolic Cu,Zn-superoxide dismutase inhibitor diethyldithiocarbamic acid, and the anion channel inhibitor 4,4'-diisothiocyanato-stilbene-2,2'-disulfonate, all of which also abrogated protection. ROS generation during hypoxia was attenuated by myxothiazol, but not by diphenyleneiodonium or the nitric-oxide synthase inhibitor L-nitroarginine. We conclude that hypoxia increases mitochondrial superoxide generation which initiates preconditioning protection. Furthermore, mitochondrial anion channels and cytosolic dismutation to H2O2 may be important steps for oxidant induction of hypoxic preconditioning.
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Diazoxide and ischemic preconditioning-associated ROS production is attenuated by myxothiazol, indicating that the Qo site of complex III is the source.
“Importantly, diazoxide and ischemic preconditioning associated ROS production is attenuated by myxothiazol [132,134], which clearly indicates that the Q o site of complex III is the source.”
From Differential effects of complex II on mitochondrial ROS production and their relation to cardioprotective pre- and postconditioning (2013) · cites this paper as [134]
The rate of O2•− generation is chemically proportional by mass action to the O2 concentration times the rate of electron leak.
“The rate of O2•− generation is chemically proportional by mass action to the O2 concentration times the rate of electron leak (310)”
From Mitochondrial reactive oxygen species production in excitable cells: Modulators of mitochondrial and cell function (2009) · cites this paper as [310]
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Cites
Preconditioning with ischemia: a delay of lethal cell injury in ischemic myocardium.
Murry, C. E., Jennings, R. B., & Reimer, K. A. (1986) · Circulation · doi:10.1161/01.cir.74.5.1124 · Cited by 7,813 · see citing works
Angiotensin II stimulates NADH and NADPH oxidase activity in cultured vascular smooth muscle cells.
Griendling, K. K., Minieri, C. A., Ollerenshaw, J. D., & Alexander, R. W. (1994) · Circulation Research · doi:10.1161/01.res.74.6.1141 · Cited by 2,735 · see citing works
Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria
Turrens, J. F., & Boveris, A. (1980) · Biochemical Journal · doi:10.1042/bj1910421 · Cited by 1,601 · see citing works
Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria
Turrens, J. F., Alexandre, A., & Lehninger, A. L. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90293-0 · Cited by 1,214 · see citing works
Enzyme-independent formation of nitric oxide in biological tissues
Zweier, J. L., Wang, P., Samouilov, A., & Kuppusamy, P. (1995) · Nature Medicine · doi:10.1038/nm0895-804 · Cited by 788 · see citing works
Xia, Y., Dawson, V. L., Dawson, T. M., Snyder, S. H., & Zweier, J. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6770 · Cited by 718 · see citing works
Nitric Oxide and Cardiac Function
Kelly, R. A., Balligand, J., & Smith, T. W. (1996) · Circulation Research · doi:10.1161/01.res.79.3.363 · Cited by 710 · see citing works
Intracellular Signaling by Reactive Oxygen Species during Hypoxia in Cardiomyocytes
Duranteau, J., Chandel, N. S., Kulisz, A., Shao, Z., & Schumacker, P. T. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.19.11619 · Cited by 679 · see citing works
Self-citationIntracellular hydrogen peroxide and superoxide anion detection in endothelial cells
Carter, W. O., Naryanan, P. K., & Robinson, J. P. (1994) · Journal of Leukocyte Biology · doi:10.1002/jlb.55.2.253 · Cited by 636 · see citing works
HESS, M., & Manson, N. H. (1984) · Journal of Molecular and Cellular Cardiology · doi:10.1016/s0022-2828(84)80011-5 · Cited by 542 · see citing works
Ambrosio, G., Zweier, J. L., Duilio, C., Kuppusamy, P., Santoro, G., Elia, P. P., Tritto, I., Cirillo, P. L., Condorelli, M., & Chiariello, M. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)46660-9 · Cited by 515 · see citing works
Baines, C. P., Goto, M., & Downey, J. M. (1997) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.1996.0265 · Cited by 484 · see citing works
Thannickal, V. J., & Fanburg, B. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.51.30334 · Cited by 424 · see citing works
Gopalakrishna, R., & Anderson, W. B. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.17.6758 · Cited by 409 · see citing works
Hoek, T. L. V., Li, C., Shao, Z., Schumacker, P. T., & Becker, L. B. (1997) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.1997.0497 · Cited by 398 · see citing works
Self-citationMitochondria as a source of reactive oxygen species during reductive stress in rat hepatocytes
Dawson, T. L., Gores, G. J., Nieminen, A. L., Herman, B., & Lemasters, J. J. (1993) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1993.264.4.c961 · Cited by 346 · see citing works
Superoxide anion permeability of phospholipid membranes and chloroplast thylakoids
Takahashi, M., & Asada, K. (1983) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(83)90325-9 · Cited by 309 · see citing works
Oxygen Radicals Can Induce Preconditioning in Rabbit Hearts
Tritto, I., D’Andrea, D., Eramo, N., Scognamiglio, A., De Simone, C., Violante, A., Esposito, A., Chiariello, M., & Ambrosio, G. (1997) · Circulation Research · doi:10.1161/01.res.80.5.743 · Cited by 288 · see citing works
Wever, R. M. F., van Dam, T., van Rijn, H. J. M., de Groot, F. G., & Rabelink, T. J. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.7069 · Cited by 281 · see citing works
Lo, L., Koch, C. J., & Wilson, D. F. (1996) · Analytical Biochemistry · doi:10.1006/abio.1996.0144 · Cited by 242 · see citing works
Myxothiazol, a new inhibitor of the cytochrome b-c1 segment of the respiratory chain
Thierbach, G., & Reichenbach, H. (1981) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(81)90238-3 · Cited by 236 · see citing works
Activation of endothelial cell phospholipase D by hydrogen peroxide and fatty acid hydroperoxide.
Natarajan, V., Taher, M. M., Roehm, B., Parinandi, N. L., Schmid, H. H. O., Kiss, Z., & Garcia, J. G. N. (1993) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)54023-0 · Cited by 211 · see citing works
The Murine Voltage-dependent Anion Channel Gene Family
Sampson, M. J., Lovell, R. S., & Craigen, W. J. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.30.18966 · Cited by 198 · see citing works
Zhou, X., Zhai, X., & Ashraf, M. (1996) · Circulation · doi:10.1161/01.cir.93.6.1177 · Cited by 184 · see citing works
Vanden Hoek, T. L., Shao, Z., Li, C., Schumacker, P. T., & Becker, L. B. (1997) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.1997.0481 · Cited by 161 · see citing works
Self-citationTanaka, M., Fujiwara, H., Yamasaki, K., & Sasayama, S. (1994) · Cardiovascular Research · doi:10.1093/cvr/28.7.980 · Cited by 143 · see citing works
Lactate and P o 2 Modulate Superoxide Anion Production in Bovine Cardiac Myocytes
Mohazzab-H., K. M., Kaminski, P. M., & Wolin, M. S. (1997) · Circulation · doi:10.1161/01.cir.96.2.614 · Cited by 140 · see citing works
Strickler, J. H., Jacobson, K. A., & Liang, B. T. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118976 · Cited by 134 · see citing works
Larsson, R. L., & Cerutti, P. (1989) · PubMed · Cited by 129 · see citing works
Myocardial damage during ischaemia and reperfusion
Fabiani, R., Ceconi, C., Curello, S., Alfieri, O., & Visioli, O. (1993) · European Heart Journal · doi:10.1093/eurheartj/14.suppl_g.25 · Cited by 119 · see citing works
Reaction of copper-zinc superoxide dismutase with diethyldithiocarbamate.
Misra, H. P. (1979) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)86530-4 · Cited by 116 · see citing works
Endogenous production of superoxide by rabbit lungs: effects of hypoxia or metabolic inhibitors
Paky, A., Michael, J. R., Burke-Wolin, T., Wolin, M. S., & Gurtner, G. H. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.74.6.2868 · Cited by 97 · see citing works
Role of oxygen free radicals in ischemic and reperfused myocardium
Ferrari, R., Ceconi, C., Curello, S., Cargnoni, A., Pasini, E., Giuli, F. D., & Albertini, A. (1991) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/53.1.215s · Cited by 83 · see citing works
Evidence for nitric oxide generation in the cardiomyocytes: its augmentation by hypoxia
Kitakaze, M., Node, K., Komamura, K., Minamino, T., Inoue, M., Hori, M., & Kamada, T. (1995) · Journal of Molecular and Cellular Cardiology · doi:10.1016/s0022-2828(95)91335-1 · Cited by 74 · see citing works
The mitochondrial inner membrane anion channel is inhibited by DIDS
Beavis, A. D., & Davatol-Hag, H. (1996) · Journal of Bioenergetics and Biomembranes · doi:10.1007/bf02110652 · Cited by 62 · see citing works
Inhibition of DNA-ethidium bromide intercalation due to free radical attack upon DNA
Pr�tz, W. A. (1984) · Radiation and Environmental Biophysics · doi:10.1007/bf01326731 · Cited by 54 · see citing works
Ischaemic preconditioning is not mediated by oxygen derived free radicals in rats
Richard, V. J., Tron, C., & Thuillez, C. (1993) · Cardiovascular Research · doi:10.1093/cvr/27.11.2016 · Cited by 44 · see citing works
Developmental changes and control of xanthine dehydrogenases in developing chicks
Fisher, J. R., Curtis, J. L., & Woodward, W. D. (1967) · Developmental Biology · doi:10.1016/0012-1606(67)90028-0 · Cited by 44 · see citing works
Cardioprotection by nisoldipine: role of timing of administration
Ferrari, R., Curello, S., Ceconi, C., Cargnoni, A., Pasini, E., & Visioli, O. (1993) · European Heart Journal · doi:10.1093/eurheartj/14.9.1258 · Cited by 42 · see citing works
Osada, M., Takeda, S., SATO, T. A., Komori, S., & Tamura, K. (1994) · Japanese Circulation Journal-english Edition · doi:10.1253/jcj.58.259 · Cited by 29 · see citing works
Flagged first, then by citations
Research works printed but not linked: 4
- Xia, Y., Dawson, V. L., Dawson, T. M., Snyder, S. H., and Zweier, J. L. (1996) Proc. Natl. Acad. Sci. U. S. A. 93, 6770 -6774
- Gopalakrishna, R., and Anderson, W. B. (1989) Proc. Natl. Acad. Sci. U. S. A. 86, 6758 -6762
- Downey, J. M., and Cohen, M. V. (1996) in Ischaemia: Preconditioning and Adaptation (Marber, M. M., and Yellon, D. M., eds) pp. 21-34, UCL Molec- ular Pathology Series, BIOS Scientific Publishers Ltd., Oxford, United Kingdom
- Duranteau, J., Chandel, N. S., Kulisz, A., Shao, Z., and Schumacker, P. T. (1998) J. Biol. Chem. 273, in press
Cited by
Sorted by citations
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
Zorov, D. B., Juhaszova, M., & Sollott, S. J. (2014) · Physiological Reviews · doi:10.1152/physrev.00026.2013 · Cited by 5,383 · see citing works
Antioxidant enzymes and human diseases
MatÉs, J. M., Pérez-Gómez, C., & De Castro, I. N. (1999) · Clinical Biochemistry · doi:10.1016/s0009-9120(99)00075-2 · Cited by 2,099 · see citing works
Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury
Azzam, E. I., Jay‐Gerin, J., & Pain, D. (2011) · Cancer Letters · doi:10.1016/j.canlet.2011.12.012 · Cited by 1,611 · see citing works
Mechanisms of Cell Death in Oxidative Stress
Ryter, S. W., Kim, H. P., Hoetzel, A., Park, J. W., Nakahira, K., Wang, X., & Choi, A. M. K. (2006) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.9.49 · Cited by 1,262 · see citing works
Halestrap, A. P. (2003) · Cardiovascular Research · doi:10.1016/s0008-6363(03)00533-9 · Cited by 1,223 · see citing works
Mitochondria and reactive oxygen species
Kowaltowski, A. J., de Souza-Pinto, N. C., Castilho, R. F., & Vercesi, A. E. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.05.004 · Cited by 1,162 · see citing works
Guzy, R. D., & Schumacker, P. T. (2006) · Experimental Physiology · doi:10.1113/expphysiol.2006.033506 · Cited by 881 · see citing works
Self-citationNew concepts in reactive oxygen species and cardiovascular reperfusion physiology
Becker, L. C. (2003) · Cardiovascular Research · doi:10.1016/j.cardiores.2003.10.025 · Cited by 703 · see citing works
Self-citationHypoxia Tolerance in Reptiles, Amphibians, and Fishes: Life with Variable Oxygen Availability
Bickler, P. E., & Buck, L. T. (2007) · Annual Review of Physiology · doi:10.1146/annurev.physiol.69.031905.162529 · Cited by 687 · see citing works
Koumenis, C., Naczki, C., Koritzinsky, M., Rastani, S., Diehl, J. A., Sonenberg, N., Koromilas, A. E., & Wouters, B. G. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.21.7405-7416.2002 · Cited by 688 · see citing works
Reactive Oxygen Species in the Regulation of Synaptic Plasticity and Memory
Massaad, C. A., & Klann, E. (2011) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3208 · Cited by 635 · see citing works
A novel protective effect of erythropoietin in the infarcted heart
Parsa, C. J., Matsumoto, A., Kim, J. H., Riel, R. U., Pascal, L. S., Walton, G. B., Thompson, R. B., Petrofski, J. A., Annex, B. H., Stamler, J. S., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci18200 · Cited by 543 · see citing works
Molecular Mechanisms of Superoxide Production by the Mitochondrial Respiratory Chain
Dröse, S., & Brandt, U. (2012) · Advances in experimental medicine and biology · doi:10.1007/978-1-4614-3573-0_6 · Cited by 519 · see citing works
Aon, M. A., Cortassa, S., Marbán, E., & O'Rourke, B. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302673200 · Cited by 521 · see citing works
High glucose‐induced oxidative stress and mitochondrial dysfunction in neurons
Russell, J. W., Golovoy, D., Vincent, A. M., Mahendru, P., Olzmann, J. A., Mentzer, A., & Feldman, E. L. (2002) · The FASEB Journal · doi:10.1096/fj.01-1027com · Cited by 520 · see citing works
Tahara, E. B., Navarete, F. D. T., & Kowaltowski, A. J. (2009) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2009.02.008 · Cited by 479 · see citing works
Sarcolemmal Versus Mitochondrial ATP-Sensitive K+Channels and Myocardial Preconditioning
Gross, G. J., & Fryer, R. M. (1999) · Circulation Research · doi:10.1161/01.res.84.9.973 · Cited by 478 · see citing works
Stowe, D. F., & Camara, A. K. S. (2009) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2331 · Cited by 471 · see citing works
Mitochondrial Function, Biology, and Role in Disease
Murphy, E., Ardehali, H., Balaban, R. S., DiLisa, F., Dorn, G. W., Kitsis, R. N., Otsu, K., Ping, P., Rizzuto, R., Sack, M. N., et al. (2016) · Circulation Research · doi:10.1161/res.0000000000000104 · Cited by 459 · see citing works
Mammalian Oxygen Sensing, Signalling and Gene Regulation
Wenger, R. H. (2000) · Journal of Experimental Biology · doi:10.1242/jeb.203.8.1253 · Cited by 444 · see citing works
Hypoxic pulmonary vasoconstriction
Moudgil, R., Michelakis, E. D., & Archer, S. L. (2004) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00733.2004 · Cited by 452 · see citing works
Evidence for Mitochondrial K + Channels and Their Role in Cardioprotection
O'Rourke, B. P. (2004) · Circulation Research · doi:10.1161/01.res.0000117583.66950.43 · Cited by 444 · see citing works
Induction of HIF–1α in response to hypoxia is instantaneous
Jewell, U. R., Kvietikova, I., Scheid, A., Bauer, C., Wenger, R. H., & Gassmann, M. (2001) · The FASEB Journal · doi:10.1096/fj.00-0732fje · Cited by 443 · see citing works
Chen, Z., Chua, C. C., Ho, Y., Hamdy, R. C., & Chua, B. H. L. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.280.5.h2313 · Cited by 421 · see citing works
Hypoxia induces severe right ventricular dilatation and infarction in heme oxygenase-1 null mice
Yet, S., Perrella, M. A., Layne, M. D., Hsieh, C.-M., Maemura, K., Kobzik, L., Wiesel, P., Christou, H. A., Kourembanas, S., & Lee, M.-E. (1999) · Journal of Clinical Investigation · doi:10.1172/jci6163 · Cited by 407 · see citing works
Ischemia/Reperfusion Injury Revisited: An Overview of the Latest Pharmacological Strategies
Soares, R. O. D. S., Losada, D. M., Jordani, M. C., Évora, P. R. B., & Castro-e-Silva, O. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20205034 · Cited by 415 · see citing works
Hypoxia-induced reactive oxygen species formation in skeletal muscle
Clanton, T. L. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01298.2006 · Cited by 401 · see citing works
Diazoxide-Induced Cardioprotection Requires Signaling Through a Redox-Sensitive Mechanism
Forbes, R. A., Steenbergen, C., & Murphy, E. (2001) · Circulation Research · doi:10.1161/hh0801.089342 · Cited by 395 · see citing works
Liu, J., Tian, J., Haas, M., Shapiro, J. I., Askari, A., & Xie, Z. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002950200 · Cited by 391 · see citing works
The role of mitochondria in protection of the heart by preconditioning
Halestrap, A. P., Clarke, S. J., & Khaliulin, I. (2007) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2007.05.008 · Cited by 390 · see citing works
Raedschelders, K., Ansley, D. M., & Chen, D. D. Y. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.11.004 · Cited by 387 · see citing works
The mechanism of mitochondrial superoxide production by the cytochrome bc1 complex
Dröse, S., & Brandt, U. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m803236200 · Cited by 386 · see citing works
Redox-optimized ROS balance: A unifying hypothesis
Aon, M. A., Cortassa, S. C., & O'Rourke, B. P. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.02.016 · Cited by 376 · see citing works
Superoxide generation by complex III: From mechanistic rationales to functional consequences
Bleier, L., & Dröse, S. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.12.002 · Cited by 369 · see citing works
Oxidative Stress and Programmed Cell Death in Diabetic Neuropathy
Vincent, A. M., Brownlee, M., & Russell, J. W. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb02108.x · Cited by 362 · see citing works
Hypoxia Triggers Subcellular Compartmental Redox Signaling in Vascular Smooth Muscle Cells
Waypa, G. B., Marks, J. D., Guzy, R. D., Mungai, P. T., Schriewer, J. M., Đokić, D., & Schumacker, P. T. (2009) · Circulation Research · doi:10.1161/circresaha.109.206334 · Cited by 358 · see citing works
Self-citationJavadov, S. A., Clarke, S. J., Das, M., Griffiths, E. J., Lim, K. H. H., & Halestrap, A. P. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.034231 · Cited by 350 · see citing works
Myocardial KATPChannels in Preconditioning
O'Rourke, B. P. (2000) · Circulation Research · doi:10.1161/01.res.87.10.845 · Cited by 349 · see citing works
Mitochondria and ischemia–reperfusion injury of the heart: Fixing a hole
Lisa, F. D., & Bernardi, P. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.01.016 · Cited by 341 · see citing works
Manganese neurotoxicity and the role of reactive oxygen species
Martinez‐Finley, E. J., Gavin, C. E., Aschner, M., & Gunter, T. E. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.01.032 · Cited by 334 · see citing works
Garlid, K., Santos, P. D. D., Xie, Z., Costa, A. D. T., & Pauček, P. (2003) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/s0005-2728(03)00109-9 · Cited by 332 · see citing works
Xie, Z., Kometiani, P. A., Liu, J., Li, J., Shapiro, J. I., & Askari, A. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.27.19323 · Cited by 332 · see citing works
Goncalves, R. L. S., Quinlan, C. L., Perevoshchikova, I. V., Hey-Mogensen, M., & Brand, M. D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.619072 · Cited by 329 · see citing works
Keeley, T. P., & Mann, G. E. (2019) · Physiological Reviews · doi:10.1152/physrev.00041.2017 · Cited by 329 · see citing works
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Schulz, R. (2001) · Cardiovascular Research · doi:10.1016/s0008-6363(01)00384-4 · Cited by 327 · see citing works
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Gross, G. J., & Peart, J. N. (2003) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00421.2003 · Cited by 324 · see citing works
K<sub>ATP</sub> channel‐independent targets of diazoxide and 5‐hydroxydecanoate in the heart
Hanley, P. J., Mickel, M., Löffler, M., Brandt, U., & Daut, J. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.023960 · Cited by 320 · see citing works
Mitochondrial reactive oxygen species production and elimination
Nickel, A. G., Kohlhaas, M., & Maack, C. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2014.03.011 · Cited by 318 · see citing works
Preconditioning in Cardiomyocytes Protects by Attenuating Oxidant Stress at Reperfusion
Hoek, T. L. V., Becker, L. B., Shao, Z., Li, C., & Schumacker, P. T. (2000) · Circulation Research · doi:10.1161/01.res.86.5.541 · Cited by 312 · see citing works
Self-citationKim, J.-S., Jin, Y., & Lemasters, J. J. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00683.2005 · Cited by 310 · see citing works
Batandier, C., Guigas, B., Détaille, D., El-Mir, M. Y. A., Fontaine, E. M., Rigoulet, M., & Leverve, X. M. (2006) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-006-9003-8 · Cited by 306 · see citing works
Xiao, L., Pimentel, D. R., Wang, J., Singh, K., Colucci, W. S., & Sawyer, D. B. (2002) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00254.2001 · Cited by 300 · see citing works
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Kulisz, A., Chen, N., Chandel, N. S., Shao, Z., & Schumacker, P. T. (2002) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00326.2001 · Cited by 287 · see citing works
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Loor, G., & Schumacker, P. T. (2008) · Cell Death and Differentiation · doi:10.1038/cdd.2008.13 · Cited by 276 · see citing works
Self-citationMechanisms of Cardioprotection by Volatile Anesthetics
Tanaka, K., Ludwig, L. M., Kersten, J. R., Pagel, P. S., & Warltier, D. C. (2004) · Anesthesiology · doi:10.1097/00000542-200403000-00035 · Cited by 274 · see citing works
Kevin, L. G., Camara, A. K. S., Riess, M. L., Novalija, E., & Stowe, D. F. (2003) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00711.2002 · Cited by 272 · see citing works
Caspase 3 activation is essential for neuroprotection in preconditioning
McLaughlin, B., Hartnett, K. A., Erhardt, J. A., Legos, J. J., White, R. F., Barone, F. C., & Aizenman, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0232966100 · Cited by 271 · see citing works
The mitochondrial permeability transition pore as a target for preconditioning and postconditioning
Hausenloy, D. J., Ong, S., & Yellon, D. M. (2009) · Basic Research in Cardiology · doi:10.1007/s00395-009-0010-x · Cited by 268 · see citing works
Reis, J. F., Monteiro, V. S., Gomes, R. D. S., do Carmo, M. M., da Costa, G. V., Ribera, P. C., & Monteiro, M. C. (2016) · Journal of Translational Medicine · doi:10.1186/s12967-016-1076-5 · Cited by 265 · see citing works
Mitochondrial Ion Channels: Gatekeepers of Life and Death
O'Rourke, B. P., Cortassa, S. C., & Aon, M. A. (2005) · Physiology · doi:10.1152/physiol.00020.2005 · Cited by 254 · see citing works
Biochemical dysfunction in heart mitochondria exposed to ischaemia and reperfusion
Solaini, G., & Harris, D. A. (2005) · Biochemical Journal · doi:10.1042/bj20042006 · Cited by 248 · see citing works
Low-Energy Laser Irradiation Promotes Cellular Redox Activity
Lubart, R., Eichler, M., Lavi, R., Friedman, H., & Shainberg, A. (2005) · Photomedicine and Laser Surgery · doi:10.1089/pho.2005.23.3 · Cited by 248 · see citing works
Cai, Z., Zhong, H., Bosch‐Marcé, M., Fox-Talbot, K., Wang, L., Wei, C., Trush, M. A., & Semenza, G. L. (2007) · Cardiovascular Research · doi:10.1093/cvr/cvm035 · Cited by 244 · see citing works
Oxidative pathways in cardiovascular disease: roles, mechanisms, and therapeutic implications
Wattanapitayakul, S. K. (2001) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(00)00114-5 · Cited by 239 · see citing works
Suzuki, Y., Jain, V., Park, A.-M., & Day, R. M. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.01.008 · Cited by 239 · see citing works
Hermes‐Lima, M., Moreira, D. C., Rivera‐Ingraham, G. A., Giraud‐Billoud, M., Genaro‐Mattos, T. C., & Campos, E. G. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.07.156 · Cited by 241 · see citing works
Lecour, S., Smith, R. M., Woodward, B. D., Opie, L. H., Rochette, L., & Sack, M. N. (2002) · Journal of Molecular and Cellular Cardiology · doi:10.1006/jmcc.2002.1533 · Cited by 235 · see citing works
Renal ischemia–reperfusion injury: Renal dendritic cells loudly sound the alarm
Nelson, P.-J. (2007) · Kidney International · doi:10.1038/sj.ki.5002121 · Cited by 232 · see citing works
The role of mitochondria in ischemia/reperfusion injury
Jassem, W., Fuggle, S. V., Rela, M., Koo, D. D. H., & Heaton, N. D. (2002) · Transplantation · doi:10.1097/00007890-200202270-00001 · Cited by 231 · see citing works
A novel mitochondriotoxic small molecule that selectively inhibits tumor cell growth
Fantin, V. R., Berardi, M. J., Scorrano, L., Korsmeyer, S. J., & Leder, P. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00082-x · Cited by 228 · see citing works
ROS and NO trigger early preconditioning: relationship to mitochondrial K<sub>ATP</sub> channel
Lebuffe, G., Schumacker, P. T., Shao, Z.-H., Anderson, T., Iwase, H., & Vanden Hoek, T. L. (2003) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00706.2002 · Cited by 227 · see citing works
Self-citationCell death during ischemia: relationship to mitochondrial depolarization and ROS generation
Levraut, J., Iwase, H., Shao, Z. H., Hoek, T. L. V., & Schumacker, P. T. (2003) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00708.2002 · Cited by 226 · see citing works
Self-citationProtein Oxidative Modifications: Beneficial Roles in Disease and Health.
Cai, Z., & Yan, L. (2013) · PubMed · Cited by 226 · see citing works
Endothelial permeability and IL-6 production during hypoxia: role of ROS in signal transduction
Ali, M. H., Schlidt, S. A., Chandel, N. S., Hynes, K. L., Schumacker, P. T., & Gewertz, B. L. (1999) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1999.277.5.l1057 · Cited by 221 · see citing works
Self-citationCardioprotection: A radical view
Penna, C. R. R., Mancardi, D., Rastaldo, R., & Pagliaro, P. (2009) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2009.02.008 · Cited by 219 · see citing works
Lim, K. H. H., Javadov, S. A., Das, M., Clarke, S. J., Suleiman, M. S., & Halestrap, A. P. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.031484 · Cited by 219 · see citing works
HANLEY, P., & DAUT, J. (2005) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2005.04.002 · Cited by 218 · see citing works
Opening mitoKATPincreases superoxide generation from complex I of the electron transport chain
Andrukhiv, A., Costa, A. D. T., West, I. C., & Garlid, K. (2006) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00272.2006 · Cited by 216 · see citing works
Role of redox metabolism for adaptation of aquatic animals to drastic changes in oxygen availability
Welker, A. F., Moreira, D. C., Campos, E. G., & Hermes‐Lima, M. (2013) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2013.04.003 · Cited by 214 · see citing works
Acute oxidative stress and systemic Nrf2 activation by the ketogenic diet
Milder, J. B., Liang, L., & Patel, M. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.05.030 · Cited by 214 · see citing works
Mitochondrial oxidant stress triggers cell death in simulated ischemia–reperfusion
Loor, G., Kondapalli, J., Iwase, H., Chandel, N. S., Waypa, G. B., Guzy, R. D., Hoek, T. L. V., & Schumacker, P. T. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.12.008 · Cited by 214 · see citing works
Self-citationMitochondrial K channels in cell survival and death
Ardehali, H., & O'Rourke, B. P. (2005) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2004.12.003 · Cited by 211 · see citing works
Costa, A. D. T., Jakob, R., Costa, C. L., Andrukhiv, K., West, I. C., & Garlid, K. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600959200 · Cited by 210 · see citing works
Zhang, D. X., Chen, Y., Campbell, W. B., Zou, A.-P., Gross, G. J., & Li, P. (2001) · Circulation Research · doi:10.1161/hh2401.101752 · Cited by 203 · see citing works
Dröse, S. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2013.01.004 · Cited by 201 · see citing works
Mechanism of Cardioprotection by Early Ischemic Preconditioning
Yang, X., Cohen, M. V., & Downey, J. M. (2010) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-010-6236-x · Cited by 201 · see citing works
Crosstalk Between Calcium and Redox Signaling: From Molecular Mechanisms to Health Implications
Hidalgo, C., & Donoso, P. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1886 · Cited by 221 · see citing works
The direct physiological effects of mitoKATPopening on heart mitochondria
Costa, A. D. T., Quinlan, C. L., Andrukhiv, A., West, I. C., Jabůrek, M., & Garlid, K. (2005) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00794.2005 · Cited by 195 · see citing works
O 2 sensing, mitochondria and ROS signaling: The fog is lifting
Waypa, G. B., Smith, K. A., & Schumacker, P. T. (2016) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2016.01.002 · Cited by 190 · see citing works
Self-citationLo, L., & Chu, C. (2003) · Chemical Communications · doi:10.1039/b309393j · Cited by 191 · see citing works
Mechanism of Superoxide Generation by Neuronal Nitric-oxide Synthase
Pou, S., Keaton, L., Surichamorn, W., & Rosen, G. M. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.14.9573 · Cited by 190 · see citing works
Heme Oxygenase-1: Molecular Mechanisms of Gene Expression in Oxygen-Related Stress
Ryter, S. W., & Choi, A. M. K. (2002) · Antioxidants and Redox Signaling · doi:10.1089/15230860260220120 · Cited by 189 · see citing works
Khan, S. A., Salloum, F. N., Das, A., Xi, L., Vetrovec, G. W., & Kukreja, R. C. (2006) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2006.04.014 · Cited by 189 · see citing works
Lavi, R., Shainberg, A., Friedmann, H., Shneyvays, V., Rickover, O., Eichler, M., Kaplan, D., & Lubart, R. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303034200 · Cited by 187 · see citing works
Opening mitochondrial K ATP in the heart - what happens, and what does not happen
Garlid, K. D. (2000) · Basic Research in Cardiology · doi:10.1007/s003950070046 · Cited by 186 · see citing works
Salnikow, K., Su, W.-C., Blagosklonny, M. V., & Costa, M. (2000) · PubMed · Cited by 186 · see citing works
Iron Homeostasis in the Neonate
Collard, K. J. (2009) · PEDIATRICS · doi:10.1542/peds.2008-1047 · Cited by 182 · see citing works
Generator-specific targets of mitochondrial reactive oxygen species
Bleier, L., Wittig, I., Heide, H., Steger, M., Brandt, U., & Dröse, S. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.10.511 · Cited by 183 · see citing works
Use the Protonmotive Force: Mitochondrial Uncoupling and Reactive Oxygen Species
Berry, B. J., Trewin, A. J., Amitrano, A. M., Kim, M., & Wojtovich, A. P. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.03.025 · Cited by 175 · see citing works
- Authors
- Vanden Hoek, T. L., Becker, L. B., Shao, Z., Li, C., & Schumacker, P. T.
- Affiliations
- University of Chicago (US)
- Corresponding author
- Schumacker, Paul T.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1998-07
- Volume
- 273
- Issue
- 29
- Pages
- 18092-18098
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2145047965
- Cited by
- 721
- References
- 40
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 7 · 2023: 4 · 2022: 4 · 2021: 15 · 2020: 10 · 2019: 8 · 2018: 11 · 2017: 8 · 2016: 29 · 2015: 16 · 2014: 31 · 2013: 33 · 2012: 26
- FWCI
- 20.19
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5k08hl003779-02, HL35440)
- National Heart, Lung, and Blood Institute (HL 32646, HL-03779, R01HL035440, HL35440)
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Cardiac Ischemia and Reperfusion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Keywords
- reactive oxygen species, mitochondrial superoxide, hypoxia, cardioprotection, preconditioning, cardiomyocytes, ischemia-reperfusion injury, hydrogen peroxide, superoxide dismutase, DIDS, myxothiazol, nitric oxide synthase, cell death
- MeSH terms
- Animals, Cells, Cultured, Chick Embryo, Cytosol, Ditiocarb, Enzyme Inhibitors, Hydrogen Peroxide, Tiopronin, Methacrylates, Mitochondria, Heart, Myocardial Contraction, Onium Compounds, Superoxide Dismutase, Thiazoles, Cell Hypoxia, Cell Death, Reactive Oxygen Species, Nitric Oxide Synthase, Ischemic Preconditioning, Myocardial
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