To die or to sleep, perhaps to dream

被引:11
作者
Gasic, GP
Nicotera, P
机构
[1] Univ Leicester, MRC, Toxicol Unit, Leicester LE1 911N, Leics, England
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Radiol,Athinoula Martinos Ctr Biomed Imaging, Boston, MA USA
关键词
apoptosis; excitotoxicity; neurodegenerative and psychiatric diseases; synaptic loss; neuronal dysfunction;
D O I
10.1016/S0378-4274(02)00487-3
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Establishing social contacts is the raison d'(e) over cap tre of neurons throughout their entire life span. To form and retain functional connections, neuronal differentiation and death are ruthlessly regulated in development and kept strictly under control in post-mitotic systems. Derangements in neural networks affect neuronal populations at large. Therefore, failure to retain synaptic connectivity is linked to dysfunction and often followed by neuronal death. Loss of neurons is a predominant feature of neurodegenerative disease. Nevertheless, neuronal cell death is not an obligate requirement for neural dysfunction at the level of distributed circuits or local circuits. Although more or less wide spread neuronal loss can occur after acute insults such as brain ischemia or invasion of the brain by pathogens, neuronal death is a hallmark of end-stage neurodegenerative and psychiatric disease. The relative contributions made by loss of synaptic connectivity versus cell death for these diseases are still debated. Here these processes are discussed in relation to acute and chronic CNS disorders. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:221 / 227
页数:7
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共 50 条
[1]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[2]  
Beilharz Erica J., 1995, Molecular Brain Research, V29, P1, DOI 10.1016/0169-328X(94)00217-3
[3]  
Bonfoco E, 1996, J NEUROCHEM, V67, P2484
[4]  
BONFOCO E, 1995, P NATL ACAD SCI USA, V92, P72162
[5]  
BREITER HC, 2002, UNPUB GEN CIRCUITRY
[6]   Strategies for neuroprotection with glutamate antagonists - Extrapolating from evidence taken from the first stroke and head injury studies [J].
Bullock, R .
NEUROPROTECTIVE AGENTS: CLINICAL AND EXPERIMENTAL ASPECTS, 1995, 765 :272-278
[7]   The lipid peroxidation product 4-hydroxy-2,3-nonenal increases AP-1-binding activity through caspase activation in neurons [J].
Camandola, S ;
Poli, G ;
Mattson, MP .
JOURNAL OF NEUROCHEMISTRY, 2000, 74 (01) :159-168
[8]   N-G-nitro-L-arginine methyl ester reduces necrotic but not apoptotic cell death induced by reversible focal ischemia in rat [J].
CharriautMarlangue, C ;
Margaill, I ;
Borrega, F ;
Plotkine, M ;
BenAri, Y .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 310 (2-3) :137-140
[9]   NGF AND BFGF PROTECT RAT HIPPOCAMPAL AND HUMAN CORTICAL-NEURONS AGAINST HYPOGLYCEMIC DAMAGE BY STABILIZING CALCIUM HOMEOSTASIS [J].
CHENG, B ;
MATTSON, MP .
NEURON, 1991, 7 (06) :1031-1041
[10]   Wiring optimization in cortical circuits [J].
Chklovskii, DB ;
Schikorski, T ;
Stevens, CF .
NEURON, 2002, 34 (03) :341-347