Abstract
This study investigates the relation between myocardial oxygen consumption (MVO2), function, and high energy phosphates during severe hypoxia and reoxygenation in sheep in vivo. Graded hypoxia was performed in open-chested sheep to adjust PO2 to values where rapid depletion of energy stores occurred. Highly time-resolved 31P nuclear magnetic resonance spectroscopy enabled monitoring of myocardial phosphates throughout hypoxia and recovery with simultaneous MVO2 measurement. Sheep undergoing graded hypoxia (n = 5) with an arterial PO2 nadir of 13.4 +/- 0.5 mmHg, demonstrated maintained rates of oxygen consumption with large changes in coronary flow as phosphocreatine (PCr) decreased within 4 min to 40 +/- 7% of baseline. ATP utilization rate increased simultaneously 59 +/- 20%. Recovery was accompanied by marked increases in MVO2 from 2.0 +/- 0.5 to 7.2 +/- 1.9 mumol/g per min, while PCr recovery rate was 4.3 +/- 0.6 mumol/g per min. ATP decreased to 75 +/- 6% of baseline during severe hypoxia and did not recover. Sheep (n = 5) which underwent moderate hypoxia (PO2 maintained 25-35 mmHg for 10 min) did not demonstrate change in PCr or ATP. Functional and work assessment (n = 4) revealed that cardiac power increased during the graded hypoxia and was maintained through early reoxygenation. These studies show that (a) MVO2 does not decrease during oxygen deprivation in vivo despite marked and rapid decreases in high energy phosphates; (b) contractile function during hypoxia in vivo does not decrease during periods of PCr depletion and intracellular phosphate accumulation, and this may be related to marked increases in circulating catecholamines during global hypoxia. The measured creatine rephosphorylation rate is 34 +/- 11% of predicted (P < 0.01) calculated from reoxygenation parameters, which indicates that some mitochondrial respiratory uncoupling also occurs during the rephosphorylation period.
Full text
PDF








Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ambrosio G., Jacobus W. E., Bergman C. A., Weisman H. F., Becker L. C. Preserved high energy phosphate metabolic reserve in globally "stunned" hearts despite reduction of basal ATP content and contractility. J Mol Cell Cardiol. 1987 Oct;19(10):953–964. doi: 10.1016/s0022-2828(87)80568-0. [DOI] [PubMed] [Google Scholar]
- BERNE R. M., BLACKMON J. R., GARDNER T. H. Hypoxemia and coronary blood flow. J Clin Invest. 1957 Jul;36(7):1101–1106. doi: 10.1172/JCI103505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bernstein D., Teitel D. F. Myocardial and systemic oxygenation during severe hypoxemia in ventilated lambs. Am J Physiol. 1990 Jun;258(6 Pt 2):H1856–H1864. doi: 10.1152/ajpheart.1990.258.6.H1856. [DOI] [PubMed] [Google Scholar]
- Crompton M., Ellinger H., Costi A. Inhibition by cyclosporin A of a Ca2+-dependent pore in heart mitochondria activated by inorganic phosphate and oxidative stress. Biochem J. 1988 Oct 1;255(1):357–360. [PMC free article] [PubMed] [Google Scholar]
- Dhalla N. S., Yates J. C., Walz D. A., McDonald V. A., Olson R. E. Correlation between changes in the endogenous energy stores and myocardial function due to hypoxia in the isolated perfused rat heart. Can J Physiol Pharmacol. 1972 Apr;50(4):333–345. doi: 10.1139/y72-050. [DOI] [PubMed] [Google Scholar]
- Drummond G. I., Severson D. L. Cyclic nucleotides and cardiac function. Circ Res. 1979 Feb;44(2):145–153. doi: 10.1161/01.res.44.2.145. [DOI] [PubMed] [Google Scholar]
- Duchen M. R., McGuinness O., Brown L. A., Crompton M. On the involvement of a cyclosporin A sensitive mitochondrial pore in myocardial reperfusion injury. Cardiovasc Res. 1993 Oct;27(10):1790–1794. doi: 10.1093/cvr/27.10.1790. [DOI] [PubMed] [Google Scholar]
- Ferrari R., Ceconi C., Curello S., Cargnoni A., Condorelli E., Belloli S., Albertini A., Visioli O. Metabolic changes during post-ischaemic reperfusion. J Mol Cell Cardiol. 1988 Mar;20 (Suppl 2):119–133. doi: 10.1016/0022-2828(88)90337-9. [DOI] [PubMed] [Google Scholar]
- Ferrari R., Pedersini P., Bongrazio M., Gaia G., Bernocchi P., Di Lisa F., Visioli O. Mitochondrial energy production and cation control in myocardial ischaemia and reperfusion. Basic Res Cardiol. 1993 Sep-Oct;88(5):495–512. doi: 10.1007/BF00795415. [DOI] [PubMed] [Google Scholar]
- Fisher D. J., Heymann M. A., Rudolph A. M. Myocardial oxygen and carbohydrate consumption in fetal lambs in utero and in adult sheep. Am J Physiol. 1980 Mar;238(3):H399–H405. doi: 10.1152/ajpheart.1980.238.3.H399. [DOI] [PubMed] [Google Scholar]
- Hardy L., Clark J. B., Darley-Usmar V. M., Smith D. R., Stone D. Reoxygenation-dependent decrease in mitochondrial NADH:CoQ reductase (Complex I) activity in the hypoxic/reoxygenated rat heart. Biochem J. 1991 Feb 15;274(Pt 1):133–137. doi: 10.1042/bj2740133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heineman F. W., Eng J., Berkowitz B. A., Balaban R. S. NMR spectral analysis of kinetic data using natural lineshapes. Magn Reson Med. 1990 Mar;13(3):490–497. doi: 10.1002/mrm.1910130316. [DOI] [PubMed] [Google Scholar]
- Herrmann S. C., Feigl E. O. Adrenergic blockade blunts adenosine concentration and coronary vasodilation during hypoxia. Circ Res. 1992 Jun;70(6):1203–1216. doi: 10.1161/01.res.70.6.1203. [DOI] [PubMed] [Google Scholar]
- Kammermeier H., Roeb E., Jüngling E., Meyer B. Regulation of systolic force and control of free energy of ATP-hydrolysis in hypoxic hearts. J Mol Cell Cardiol. 1990 Jun;22(6):707–713. doi: 10.1016/0022-2828(90)91013-w. [DOI] [PubMed] [Google Scholar]
- Katz L. A., Swain J. A., Portman M. A., Balaban R. S. Intracellular pH and inorganic phosphate content of heart in vivo: a 31P-NMR study. Am J Physiol. 1988 Jul;255(1 Pt 2):H189–H196. doi: 10.1152/ajpheart.1988.255.1.H189. [DOI] [PubMed] [Google Scholar]
- Kentish J. C. The effects of inorganic phosphate and creatine phosphate on force production in skinned muscles from rat ventricle. J Physiol. 1986 Jan;370:585–604. doi: 10.1113/jphysiol.1986.sp015952. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kusachi S., Nishiyama O., Yasuhara K., Saito D., Haraoka S., Nagashima H. Right and left ventricular oxygen metabolism in open-chest dogs. Am J Physiol. 1982 Nov;243(5):H761–H766. doi: 10.1152/ajpheart.1982.243.5.H761. [DOI] [PubMed] [Google Scholar]
- Kusuoka H., Weisfeldt M. L., Zweier J. L., Jacobus W. E., Marban E. Mechanism of early contractile failure during hypoxia in intact ferret heart: evidence for modulation of maximal Ca2+-activated force by inorganic phosphate. Circ Res. 1986 Sep;59(3):270–282. doi: 10.1161/01.res.59.3.270. [DOI] [PubMed] [Google Scholar]
- Kypson J., Hait G. Myocardial metabolism and performance in hypoxia: effect of epinephrine. J Appl Physiol Respir Environ Exerc Physiol. 1978 Nov;45(5):791–796. doi: 10.1152/jappl.1978.45.5.791. [DOI] [PubMed] [Google Scholar]
- Lai F., Scheuer J. Early changes in myocardial hypoxia: relations between mechanical function, pH and intracellular compartmental metabolites. J Mol Cell Cardiol. 1975 Apr;7(4):289–303. doi: 10.1016/0022-2828(75)90086-3. [DOI] [PubMed] [Google Scholar]
- Lee J. C., Halloran K. H., Taylor J. F., Downing S. E. Coronary flow and myocardial metabolism in newborn lambs: effects of hypoxia and acidemia. Am J Physiol. 1973 Jun;224(6):1381–1387. doi: 10.1152/ajplegacy.1973.224.6.1381. [DOI] [PubMed] [Google Scholar]
- Mast F., Elzinga G. Oxidative and glycolytic ATP formation of rabbit papillary muscle in oxygen and nitrogen. Am J Physiol. 1990 Apr;258(4 Pt 2):H1144–H1150. doi: 10.1152/ajpheart.1990.258.4.H1144. [DOI] [PubMed] [Google Scholar]
- Matherne G. P., Headrick J. P., Berr S., Berne R. M. Metabolic and functional responses of immature and mature rabbit hearts to hypoperfusion, ischemia, and reperfusion. Am J Physiol. 1993 Jun;264(6 Pt 2):H2141–H2153. doi: 10.1152/ajpheart.1993.264.6.H2141. [DOI] [PubMed] [Google Scholar]
- Miyata H., Lakatta E. G., Stern M. D., Silverman H. S. Relation of mitochondrial and cytosolic free calcium to cardiac myocyte recovery after exposure to anoxia. Circ Res. 1992 Sep;71(3):605–613. doi: 10.1161/01.res.71.3.605. [DOI] [PubMed] [Google Scholar]
- Nishimura M., Takami H., Kaneko M., Nakano S., Matsuda H., Kurosawa K., Inoue T., Tagawa K. Mechanism of mitochondrial enzyme leakage during reoxygenation of the rat heart. Cardiovasc Res. 1993 Jun;27(6):1116–1122. doi: 10.1093/cvr/27.6.1116. [DOI] [PubMed] [Google Scholar]
- Noll T., Koop A., Piper H. M. Mitochondrial ATP-synthase activity in cardiomyocytes after aerobic-anaerobic metabolic transition. Am J Physiol. 1992 May;262(5 Pt 1):C1297–C1303. doi: 10.1152/ajpcell.1992.262.5.C1297. [DOI] [PubMed] [Google Scholar]
- Orchard C. H., Kentish J. C. Effects of changes of pH on the contractile function of cardiac muscle. Am J Physiol. 1990 Jun;258(6 Pt 1):C967–C981. doi: 10.1152/ajpcell.1990.258.6.C967. [DOI] [PubMed] [Google Scholar]
- Osbakken M., Mitchell M. D., Zhang D., Mayevsky A., Chance B. In vivo correlation of myocardial metabolism, perfusion, and mechanical function during increased cardiac work. Cardiovasc Res. 1991 Sep;25(9):749–756. doi: 10.1093/cvr/25.9.749. [DOI] [PubMed] [Google Scholar]
- Piper H. M., Noll T., Siegmund B. Mitochondrial function in the oxygen depleted and reoxygenated myocardial cell. Cardiovasc Res. 1994 Jan;28(1):1–15. doi: 10.1093/cvr/28.1.1. [DOI] [PubMed] [Google Scholar]
- Pool P. E., Covell J. W., Chidsey C. A., Braunwald E. Myocardial high energy phosphate stores in acutely induced hypoxic heart failure. Circ Res. 1966 Aug;19(2):221–229. doi: 10.1161/01.res.19.2.221. [DOI] [PubMed] [Google Scholar]
- Portman M. A., Heineman F. W., Balaban R. S. Developmental changes in the relation between phosphate metabolites and oxygen consumption in the sheep heart in vivo. J Clin Invest. 1989 Feb;83(2):456–464. doi: 10.1172/JCI113904. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Portman M. A. Measurement of unidirectional P(i)-->ATP flux in lamb myocardium in vivo. Biochim Biophys Acta. 1994 Apr 28;1185(2):221–227. doi: 10.1016/0005-2728(94)90213-5. [DOI] [PubMed] [Google Scholar]
- Portman M. A., Ning X. H. Developmental adaptations in cytosolic phosphate content and pH regulation in the sheep heart in vivo. J Clin Invest. 1990 Dec;86(6):1823–1828. doi: 10.1172/JCI114912. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robitaille P. M., Merkle H., Lew B., Path G., Hendrich K., Lindstrom P., From A. H., Garwood M., Bache R. J., Uğurbil K. Transmural high energy phosphate distribution and response to alterations in workload in the normal canine myocardium as studied with spatially localized 31P NMR spectroscopy. Magn Reson Med. 1990 Oct;16(1):91–116. doi: 10.1002/mrm.1910160110. [DOI] [PubMed] [Google Scholar]
- Rumsey W. L., Schlosser C., Nuutinen E. M., Robiolio M., Wilson D. F. Cellular energetics and the oxygen dependence of respiration in cardiac myocytes isolated from adult rat. J Biol Chem. 1990 Sep 15;265(26):15392–15402. [PubMed] [Google Scholar]
- Sako E. Y., Kingsley-Hickman P. B., From A. H., Foker J. E., Ugurbil K. ATP synthesis kinetics and mitochondrial function in the postischemic myocardium as studied by 31P NMR. J Biol Chem. 1988 Aug 5;263(22):10600–10607. [PubMed] [Google Scholar]
- Schaefer S., Schwartz G. G., Wisneski J. A., Trocha S. D., Christoph I., Steinman S. K., Garcia J., Massie B. M., Weiner M. W. Response of high-energy phosphates and lactate release during prolonged regional ischemia in vivo. Circulation. 1992 Jan;85(1):342–349. doi: 10.1161/01.cir.85.1.342. [DOI] [PubMed] [Google Scholar]
- Scheuer J. Myocardial metabolism in cardiac hypoxia. Am J Cardiol. 1967 Mar;19(3):385–392. doi: 10.1016/0002-9149(67)90452-3. [DOI] [PubMed] [Google Scholar]
- Schmidt-Ott S. C., Bletz C., Vahl C., Saggau W., Hagl S., Rüegg J. C. Inorganic phosphate inhibits contractility and ATPase activity in skinned fibers from human myocardium. Basic Res Cardiol. 1990 Jul-Aug;85(4):358–366. doi: 10.1007/BF01907128. [DOI] [PubMed] [Google Scholar]
- Schulz R., Guth B. D., Pieper K., Martin C., Heusch G. Recruitment of an inotropic reserve in moderately ischemic myocardium at the expense of metabolic recovery. A model of short-term hibernation. Circ Res. 1992 Jun;70(6):1282–1295. doi: 10.1161/01.res.70.6.1282. [DOI] [PubMed] [Google Scholar]
- Siegmund B., Koop A., Klietz T., Schwartz P., Piper H. M. Sarcolemmal integrity and metabolic competence of cardiomyocytes under anoxia-reoxygenation. Am J Physiol. 1990 Feb;258(2 Pt 2):H285–H291. doi: 10.1152/ajpheart.1990.258.2.H285. [DOI] [PubMed] [Google Scholar]
- Silverman H. S. Mitochondrial free calcium regulation in hypoxia and reoxygenation: relation to cellular injury. Basic Res Cardiol. 1993 Sep-Oct;88(5):483–494. doi: 10.1007/BF00795414. [DOI] [PubMed] [Google Scholar]
- Swain J. L., Sabina R. L., McHale P. A., Greenfield J. C., Jr, Holmes E. W. Prolonged myocardial nucleotide depletion after brief ischemia in the open-chest dog. Am J Physiol. 1982 May;242(5):H818–H826. doi: 10.1152/ajpheart.1982.242.5.H818. [DOI] [PubMed] [Google Scholar]
- Wittenberg B. A., Wittenberg J. B. Oxygen pressure gradients in isolated cardiac myocytes. J Biol Chem. 1985 Jun 10;260(11):6548–6554. [PubMed] [Google Scholar]
- van der Vusse G. J., Arts T., Glatz J. F., Reneman R. S. Transmural differences in energy metabolism of the left ventricular myocardium: fact or fiction. J Mol Cell Cardiol. 1990 Jan;22(1):23–37. doi: 10.1016/0022-2828(90)90969-9. [DOI] [PubMed] [Google Scholar]

