Mitochondrial hexokinase and cardioprotection of the intact heart

被引:48
作者
Zuurbier, C. J. [1 ,2 ]
Smeele, K. M. A. [1 ,2 ]
Eerbeek, O. [1 ,2 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Anaesthesiol, LEICA, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Physiol, NL-1105 AZ Amsterdam, Netherlands
关键词
Mitochondria; Preconditioning; Heart; Hexokinase; Cell death; OXYGEN SPECIES GENERATION; DEPENDENT ANION CHANNELS; RESPONSE-TIME; CELL-DEATH; RAT-HEART; GLUCOSE; PHOSPHORYLATION; REPERFUSION; APOPTOSIS; ISCHEMIA;
D O I
10.1007/s10863-009-9209-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The interaction of hexokinase with mitochondria has emerged as a powerful mechanism in protecting many cell types against cell death. However, the role of mitochondrial hexokinase (mitoHK) in cardiac ischemia-reperfusion injury has as of yet received little attention. In this review we examine whether increased binding of hexokinase to the mitochondrion is also an integral component of cardioprotective signalling. We discuss observations in cardiac mitochondrial activation that directed us to the hypothesis of hexokinase cellular redistribution with reversible, cardioprotective ischemia, summarize the data showing that many cardioprotective interventions, such as ischemic preconditioning, insulin, morphine and volatile anesthetics, increase mitochondrial hexokinase binding within the intact heart, and discuss similarities between mitochondrial hexokinase association and ischemic preconditioning. Although most data indicate that mitochondrial hexokinase may indeed be an integral part of cardioprotection, a definitive proof for a causal relation between the amount of mitoHK and cardiac ischemia-reperfusion injury in the intact heart is eagerly awaited. When such relationship is indeed observed, the association of hexokinase with mitochondria will offer an opportunity to develop new therapies to combat ischemic cardiac diseases.
引用
收藏
页码:181 / 185
页数:5
相关论文
共 40 条
[1]
Hexokinase II Detachment from Mitochondria Triggers Apoptosis through the Permeability Transition Pore Independent of Voltage-Dependent Anion Channels [J].
Chiara, Federica ;
Castellaro, Diego ;
Marin, Oriano ;
Petronilli, Valeria ;
Brusilow, William S. ;
Juhaszova, Magdalena ;
Sollott, Steven J. ;
Forte, Michael ;
Bernardi, Paolo ;
Rasola, Andrea .
PLOS ONE, 2008, 3 (03)
[2]
Inhibition of mitochondrial permeability transition pore opening by ischemic preconditioning is probably mediated by reduction of oxidative stress rather than mitochondrial protein phosphorylation [J].
Clarke, Samantha J. ;
Khaliulin, Igor ;
Das, Manika ;
Parker, Joanne E. ;
Heesom, Kate J. ;
Halestrap, Andrew P. .
CIRCULATION RESEARCH, 2008, 102 (09) :1082-1090
[3]
Is a high glycogen content beneficial or detrimental to the ischemic rat heart? A controversy resolved [J].
Cross, HR ;
Opie, LH ;
Radda, GK ;
Clarke, K .
CIRCULATION RESEARCH, 1996, 78 (03) :482-491
[4]
Mitochondrial bound hexokinase activity as a preventive antioxidant Defense -: Steady-state ADP formation as a regulatory mechanism of membrane potential and reactive oxygen species generation in mitochondria [J].
da-Silva, WS ;
Gómez-Puyou, A ;
de Gómez-Puyou, MT ;
Moreno-Sanchez, R ;
De Felice, FG ;
de Meis, L ;
Oliveira, MF ;
Galina, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (38) :39846-39855
[5]
Garlid KD, 1997, CIRC RES, V81, P1072
[6]
The pathophysiology of mitochondrial cell death [J].
Green, DR ;
Kroemer, G .
SCIENCE, 2004, 305 (5684) :626-629
[7]
Ischemic preconditioning affects hexokinase activity and HKII in different subcellular compartments throughout cardiac ischemia-reperfusion [J].
Guerel, Ebru ;
Smeele, Kirsten M. ;
Eerbeek, Otto ;
Koeman, Anneke ;
Demirci, Cihan ;
Hollmann, Markus W. ;
Zuurbier, Coert J. .
JOURNAL OF APPLIED PHYSIOLOGY, 2009, 106 (06) :1909-1916
[8]
Role of STAT3 in ischemic preconditioning [J].
Hattori, R ;
Maulik, N ;
Otani, H ;
Zhu, L ;
Cordis, G ;
Engelman, RM ;
Siddiqui, MAQ ;
Das, DK .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (11) :1929-1936
[9]
Ischemic preconditioning protects by activating prosurvival kinases at reperfusion [J].
Hausenloy, DJ ;
Tsang, A ;
Mocanu, MM ;
Yellon, DM .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2005, 288 (02) :H971-H976
[10]
Metabolism of preconditioned myocardium: Effect of loss and reinstatement of cardioprotection [J].
Jennings, RB ;
Sebbag, L ;
Schwartz, LM ;
Crago, MS ;
Reimer, KA .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (09) :1571-1588