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
[1]   Stretch-induced injury alters mitochondrial membrane potential and cellular ATP in cultured astrocytes and neurons [J].
Ahmed, SM ;
Rzigalinski, BA ;
Willoughby, KA ;
Sitterding, HA ;
Ellis, EF .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (05) :1951-1960
[2]  
Back T, 2000, ANN NEUROL, V47, P485, DOI 10.1002/1531-8249(200004)47:4<485::AID-ANA12>3.3.CO
[3]  
2-#
[4]   APOPTOSIS AND NECROSIS - 2 DISTINCT EVENTS INDUCED, RESPECTIVELY, BY MILD AND INTENSE INSULTS WITH N-METHYL-D-ASPARTATE OR NITRIC-OXIDE SUPEROXIDE IN CORTICAL CELL-CULTURES [J].
BONFOCO, E ;
KRAINC, D ;
ANKARCRONA, M ;
NICOTERA, P ;
LIPTON, SA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7162-7166
[5]   Spontaneous changes in mitochondrial membrane potential in cultured neurons [J].
Buckman, JF ;
Reynolds, IJ .
JOURNAL OF NEUROSCIENCE, 2001, 21 (14) :5054-5065
[6]   Glucose deprivation and chemical hypoxia:: neuroprotection by P2 receptor antagonists [J].
Cavaliere, F ;
D'Ambrosi, N ;
Ciotti, MT ;
Mancino, G ;
Sancesario, G ;
Bernardi, G ;
Volonté, C .
NEUROCHEMISTRY INTERNATIONAL, 2001, 38 (03) :189-197
[7]   Reversible depolarization of in situ mitochondria by oxidative stress parallels a decrease in NAD(P)H level in nerve terminals [J].
Chinopoulos, C ;
Tretter, L ;
Adam-Vizi, V .
NEUROCHEMISTRY INTERNATIONAL, 2000, 36 (06) :483-488
[8]  
Chinopoulos C, 2000, J NEUROSCI, V20, P2094
[9]   Mitochondrial function as a determinant of recovery or death in cell response to injury [J].
Di Lisa, F ;
Bernardi, P .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 184 (1-2) :379-391
[10]  
Elimadi A, 1998, J PHARMACOL EXP THER, V286, P23