Mitochondrial membrane potential and ischemic neuronal death

被引:114
作者
Iijima, Takehiko [1 ]
机构
[1] Kyorin Univ, Sch Med, Dept Anesthesiol, Mitaka, Tokyo 1818611, Japan
关键词
apoptosis; necrosis; mitochondria; hyperpolarization; membrane potential; ATP; neuronal death; ischemia;
D O I
10.1016/j.neures.2006.04.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mitochondria are intracellular organelles in which high energy phosphate is produced. Ischemia causes depletion of the materials necessary to produce this phosphate and strongly affects the electron transport chain. Apoptosis commences during and after ischemia. As such, it is likely that a significant relationship exists between inactivation of electron transport and apoptosis. Mitochondrial membrane potential (MMP) reflects performance of the electron transport chain and can indicate a pathological disorder of this system. In an experimental setting, oxygen-glucose depletion (OGD) in neuronal cell culture has been employed to simulate an ischemic condition. The relationship between MMP and subsequent neuronal death during and after OGD has been examined. MMP dissipation and concomitant neuronal death have been reported, but recent studies have demonstrated mitochondrial hyperpolarization preceding neuronal death. The direction of MMP polarization depends on the extent of OGD. Long OGD results in depolarization, while shorter OGD induces hyperpolarization. Neurons are still viable during hyperpolarization, but the process may switch on the apoptotic cascade. Meanwhile, dissipation of MMP seems to be a consequence of severe energy deficit, leading to necrosis. MMP may be a marker of subsequent apoptosis, although a causal relationship remains to be determined. (c) 2006 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:234 / 243
页数:10
相关论文
共 47 条
[31]   Activation of mitochondrial, ATP-dependent potassium channels protects neurons against ischemia-induced death by a mechanism involving suppression of bax translocation and cytochrome c release [J].
Liu, D ;
Lu, CB ;
Wan, RQ ;
Auyeung, WW ;
Mattson, MP .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2002, 22 (04) :431-443
[32]   TEMPORAL PROFILE OF HEAT-SHOCK PROTEIN-70 SYNTHESIS IN ISCHEMIC TOLERANCE INDUCED BY PRECONDITIONING ISCHEMIA IN RAT HIPPOCAMPUS [J].
LIU, Y ;
KATO, H ;
NAKATA, N ;
KOGURE, K .
NEUROSCIENCE, 1993, 56 (04) :921-927
[33]  
LOPACHIN RM, 1995, J NEUROSCI, V15, P6735
[34]   Delayed ischemic preconditioning activates nuclear-encoded electron-transfer-chain gene expression in parallel with enhanced postanoxic mitochondrial respiratory recovery [J].
McLeod, CJ ;
Jeyabalan, AP ;
Minners, JO ;
Clevenger, R ;
Hoyt, RF ;
Sack, MN .
CIRCULATION, 2004, 110 (05) :534-539
[35]   PRECONDITIONING WITH ISCHEMIA - A DELAY OF LETHAL CELL INJURY IN ISCHEMIC MYOCARDIUM [J].
MURRY, CE ;
JENNINGS, RB ;
REIMER, KA .
CIRCULATION, 1986, 74 (05) :1124-1136
[36]   Mitochondrial hyperpolarization: a checkpoint of T-cell life, death and autoimmunity [J].
Perl, A ;
Gergely, P ;
Nagy, G ;
Koncz, A ;
Banki, K .
TRENDS IN IMMUNOLOGY, 2004, 25 (07) :360-367
[37]  
Poot M, 1999, CYTOMETRY, V35, P311, DOI 10.1002/(SICI)1097-0320(19990401)35:4<311::AID-CYTO3>3.3.CO
[38]  
2-5
[39]   Dissipation of potassium and proton gradients inhibits mitochondrial hyperpolarization and cytochrome c release during neural apoptosis [J].
Poppe, M ;
Reimertz, C ;
Düssmann, H ;
Krohn, AJ ;
Luetjens, CM ;
Böckelmann, D ;
Nieminen, AL ;
Kögel, D ;
Prehn, JHM .
JOURNAL OF NEUROSCIENCE, 2001, 21 (13) :4551-4563
[40]   J-AGGREGATE FORMATION OF A CARBOCYANINE AS A QUANTITATIVE FLUORESCENT INDICATOR OF MEMBRANE-POTENTIAL [J].
REERS, M ;
SMITH, TW ;
CHEN, LB .
BIOCHEMISTRY, 1991, 30 (18) :4480-4486