Skip to main content
Log in

Early ischemia-induced alterations of the outer mitochondrial membrane and the intermembrane space: A potential cause for altered energy transfer in cardiac muscle?

  • Published:
Molecular and Cellular Biochemistry Aims and scope Submit manuscript

Abstract

Our aim was to carefully analyse the time-dependent changes that affect the mitochondrial function of myocardial cells during and after an ischemic episode. To this end, variables characterizing mitochondrial function have been evaluated on myocardial samples from isolated rat hearts subjected to different conditions of ischemia. The technique of permeabilized fibers was used in order to evaluate the mitochondrial function whilst retaining intracellular structure.

The earliest alteration that could be detected was a decrease in the stimulatory effect of creatine on mitochondrial respiration. This alteration became more pronounced as the severity (or duration) of the ischemia increased. Afterwards, a significant decrease in the apparent Km of mitochondrial respiration for ADP also appeared, followed by a diminution of the maximal respiration rate which was partly restored by adding cytochrome c. Finally, for the most severe conditions of ischemia, the basal respiratory rate also increased. These observations are indicative of a sequence of alterations affecting first the intermembrane space, then the outer mitochondrial membrane, and finally the inner membrane. The discussion is focused on the very early alterations, that could not be detected using the conventional techniques of isolated mitochondria. We postulate that these alterations to the intermembrane space and outer mitochondrial membrane can induce disturbances both in the channelling of energy from the mitochondria, and on the signalling towards the mitochondria. The potential consequences on the regulation of the production of energy (ATP, PC) by the mitochondria are evoked.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Regitz V, Paulson DJ, Hodach RJ, Little SE, Shaper W, Shug AL: Mitochondrial damage during myocardial ischemia. Basic Res Cardiol 79: 207–217, 1984

    Google Scholar 

  2. Piper HM, Noll T, Siegmund B: Mitochondrial function in the oxygen depleted and reoxygenated myocardial cells. Cardiovasc Res 28: 1–15, 1994

    Google Scholar 

  3. Brdiczka D, Wallimann T: The importance of the outer mitochondrial compartment in regulation of energy metabolism. Mol Cell Biochem 133/134: 69–83, 1994

    Google Scholar 

  4. Brdiczka D: function of the outer mitochondrial compartment in regulation of energy metabolism. Biochim Biophys Acta 1187: 264–269, 1994

    Google Scholar 

  5. Brdiczka D: Contact site between mitochondrial envelope membrane. Structure and function in energy and protein transfer. Biochim Biophys Acta 1071: 291–312, 1991

    Google Scholar 

  6. Soboll S, Conrad A, Keller M, Hebisch S: The role of the mitochondrial creatine kinase system for myocardial function during ischemia and reperfusion. Biochim Biophys Acta 1100: 27–372, 1992

    Google Scholar 

  7. Gellerich FN, Khuchua ZA, Kuznetsov AV: Influence of the mito–chondrial outer membrane and the binding of creatine kinase to the mitochondrial inner membrane on the compartmentation of adenine nucleotides in the intermembrane space of rat heart mitochondria. Biochim Biophys Acta 1140: 327–334, 1993

    Google Scholar 

  8. Rauch U, Schulze K, Witzenbichler B, Schultheiss HP: Alteration of the cytosolic-mitochondrial distribution of high-energy phosphates during global myocardial ischemia may contribute to early contractile failure. Circ Res 75: 760–769, 1994

    Google Scholar 

  9. Saks VA, Kuznetsov AV, Khuchua ZA, Vasilyeva EV, Belikova YuO, Kesvatera T, Tiivel T: Control of cellular respiration in vivo by mitochondrial outer membrane and by creatine kinase. A new speculative hypothesis: Possible involvement of mitochondrial–cytoskeleton interactions. J Mol Cell Cardiol 27: 625–645, 1995

    Google Scholar 

  10. Wyss M, Smeitink J, Wevers RA, Wallimann T: Mitochondrial creatine kinase: A key enzyme of aerobic energy metabolism. Biochim Biophys Acta (Review) 1102: 119–166, 1992

    Google Scholar 

  11. Wallimann T, Wyss M, Brdiczka D, Nicolay K, Eppenberger HM: Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the ‘phosphocreatine circuit’ for cellular energy homeostasis. Biochem J 281: 21–40, 1992

    Google Scholar 

  12. Bittl JA, Weisfeldt ML, Jacobus WE: Creatine kinase of heart mitochondria. The progressive loss of enzyme activity during in vivo ischemia and its correlation to depressed myocardial function. J Biol Chem 260: 208–214, 1985

    Google Scholar 

  13. Veksler VI, Kuznetsov AV, Sharov VG, Kapelko VI, Saks VA: Mitochondrial respiratory parameters in cardiac tissue: a novel method for assessment by using saponin-skinned fibers. Biochim Biophys Acta 892: 191–196, 1987

    Google Scholar 

  14. Saks VA, Kapelko VI, Kupriyanov VV, Kuznetsov AV, Lakomkin VL, Veksler VI, Sharov VG, Javadov SA, Seppet EK, Kairane C: Quantitative evaluation of relationship between cardiac energy metabolism and postischemic recovery of contractile function. J Mol Cell Cardiol 21: 6778, 1989

    Google Scholar 

  15. Veksler VI, Khatkevich AN, Elizarova GV, Kapelko VI: Mitochondrial respiration in myocardial biopsy samples as a criterion of postischemic recovery of the cardiac contractility. Basic Res Cardiol 85: 307–314, 1990

    Google Scholar 

  16. Kay L, Daneshrad Z, Saks V, Rossi A: Alteration in the control of mitochondrial respiration by outer mitochondrial membrane and creatine during heart preservation. Cardiovasc Res 34: 547–556, 1997

    Google Scholar 

  17. Kay L, Saks V, Rossi A: Early alteration of energy transfer in myocardial ischemia. J Moll Cell Cardiol 29: 3399–3411, 1997

    Google Scholar 

  18. Saks VA, Vasileva EV, Belikova YuO, Kuznetsov AV, Lyapina S, Petrova L, Perov NA: Retarded diffusion of ADP in cardiomyocytes: Possible role of mitochondrial outer membrane and creatine kinase in cellular regulation of oxidative phosphorylation. Biochim Biophys Acta 1144: 134–148, 1993

    Google Scholar 

  19. Saks VA, Khuchua ZA, Vasilyeva EV, Belikova Yu, Kuznetsov AV: Metabolic compartmentation and substrate channelling in muscle cells. Role of coupled creatine kinases in in vivo regulation of cellular respiration-a synthesis. Mol Cell Biochem 133/134: 155–192, 1994

    Google Scholar 

  20. Saks V, Veksler VI, Kay L, Sikk P, Tiivel T, Tranqui L, Olivares J, Kuznetsov AV, Winkler K, Wiedemann F, Kunz W: Permeabilized cell and skinned fiber techniques in studies of mitochondrial function in vivo. Mol Cell Biochem, this volume

  21. Neubauer S, Horn M, Naumann A, Tian R, Hu K, Laser M, Friedrich J, Gaudron P, Schnackerz K, Ingwall JS, Erti G: Impairment of energy metabolism in intact residual myocardium of rat hearts with chronic myocardial infarction. J Clin Invest 95: 1092–1100, 1995

    Google Scholar 

  22. Neubauer S, Hamman BL, Perry SB, Bittl JA, Ingwall JS: Velocity of the creatine kinase reaction decreases in postischemic myocardium: A 31 P-NMR magnetization transfer study of the isolated ferret heart. Cir Res 63: 1–15, 1988

    Google Scholar 

  23. Mekhfi H, Veksler V, Mateo P, Maupoil V, Rochette L, Ventura-Clapier R: Creatine kinase is the main target of reactive oxygen species in cardiac myofibrils. Circ Res 78: 1016–1027, 1996

    Google Scholar 

  24. Yuan G, Kaneko M, Masuda H, Hon RB, Kobayashi A, Yamazaki N: Decrease in heart mitochondrial creatine kinase activity due to oxygen free radicals. Biochim Biophys Acta 1140: 78–84, 1992

    Google Scholar 

  25. Jennings RB, Reimer KA, Steenbergen C: Myocardial ischemia revisited. The osmolar load, membrane damage, and reperfusion. J Mol Cell Cardiol (Editorial Comment) 18: 769–780, 1986

    Google Scholar 

  26. Hall N, DeLuca M: The effect of inorganic phosphate on creatine kinase in rat heart mitochondria. Arch Biochem Biophys 229: 477–419, 1984

    Google Scholar 

  27. Vial C, Font B, Goldschmidt D, Gautheron DC: Dissociation and reassociation of creatine kinase with heart mitochondria: pH and phosphate dependence. Biochem Biophys Res Commun 88: 1352–1359, 1979

    Google Scholar 

  28. Di Lisa F, Bernardi P: Mitochondrial function as a determinant of recovery or death in cell response to injury. Mol Cell Biochem (this volume)

  29. Yang J, Liu X, Bhalla K, Kim CN, Ibrado AM, Cai J, Peng TI Jones DP, Wang X: Prevention of apoptosis by Bc1-2: Release of cytochrome c from mitochondria blocked. Science 275: 1129, 1997

    Google Scholar 

  30. Kapelko VI, Kupriyanov VV, Novikova NA, Lakomkim VL, Steinschneider AY, Severina MY, Veksler VI Saks VA: The cardiac contractile failure induced by chronic creatine and phosphocreatine deficiency. J Mol Cell Cardiol 20: 465–479, 1988

    Google Scholar 

  31. Zweier JL, Jacobus WE, Korecky B, Brandeis-Barry Y: Bioenergetic consequences of cardiac phosphocreatine depletion induced by creatine analogue feeding. J Biol Chem 266: 20296–20304, 1991

    Google Scholar 

  32. Fossel ET, Hoefeler H: Complete inhibition of creatine kinase in isolated perfused rat hearts. Am J Physiol 252 (Endocrinol Metab 15): E124–E130, 1987

    Google Scholar 

  33. Hamman BL, Bittl JA, Jacobus WE, Allen PD, Spencer RS, Tian R, Ingwall JS: Inhibition of the creatine kinase reaction decreases the contractile reserve of isolated rat hearts. Am J Physiol 269 (Heart Circ Physiol 38): H1030–H1036, 1995

    Google Scholar 

  34. Van Beek JHGM, Westerhof N: Response times of mitochondrial oxygen consumption to heart rate steps. Am J Physiol 260: H613–H625, 1991

    Google Scholar 

  35. Van Beek JHGM, Tian X, Zuurbier CJ, De Groot B, Van Echteld CJA, Eijgelshoven MHJ, Hak JB: The dynamic regulation of myocardial oxidative phosphorylation; analysis of the response time of oxygen consumption. Mol Cell Biochem, this volume

  36. Zuurbier CJ, Beek JHGM van: The dynamic control of mitochondrial oxygen consumption in isolated perfused rabbit heart is not affected by a short period of ischemia. J Physiol 479: 71–72P, 1994

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rossi, A., Kay, L. & Saks, V. Early ischemia-induced alterations of the outer mitochondrial membrane and the intermembrane space: A potential cause for altered energy transfer in cardiac muscle?. Mol Cell Biochem 184, 401–408 (1998). https://doi.org/10.1023/A:1006874825403

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006874825403

Navigation