Pathogenesis of nigral cell death in Parkinson's disease

被引:126
作者
Przedborski, S
机构
[1] Columbia Univ, Dept Neurol, New York, NY 10032 USA
[2] Columbia Univ, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ, Ctr Neurobiol & Behav, New York, NY 10032 USA
关键词
Parkinson's disease; MPTP; neurodegeneration; pathogenesis;
D O I
10.1016/j.parkreldis.2004.10.012
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Parkinson's disease (PD) is primarily a sporadic condition which results mainly from the death of dopaminergic neurons in the substantia nigra. Its etiology remains enigmatic while its pathogenesis begins to be understood as a multifactorial cascade of deleterious factors. As of yet, most insights into PD pathogenesis are derived from toxic models of PD and show that the earlier cellular perturbations arising in dopaminergic neurons include oxidative stress and energy crisis. These alterations, rather than killing neurons, trigger subsequent death-related molecular pathways including elements of apoptosis. The fate of dopaminergic neurons in PD may also be influenced by additional factors such as excitotoxicity, emanating from the increased glutamatergic input from the subthalamic nucleus to the substantia nigra, and the glial response that arises in the striatum and the substantia nigra. In rare instances, PD can be familial, and those genetic forms have also provided clues to the pathogenesis of nigrostriatal dopaminergic neuron death including abnormalities in the mechanisms of protein folding and degradation as well as mitochondrial function. Although more remains to be elucidated about the pathogenic cascade in PD, the compilation of all of the aforementioned alterations starts to shed light on why and how nigral dopaminergic neurons may degenerate in this prominent disease, that is PD. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:S3 / S7
页数:5
相关论文
共 32 条
[1]  
[Anonymous], 2004, ADV MOL CEL
[2]   The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization [J].
Canet-Avilés, RM ;
Wilson, MA ;
Miller, DW ;
Ahmad, R ;
McLendon, C ;
Bandyopadhyay, S ;
Baptista, MJ ;
Ringe, D ;
Petsko, GA ;
Cookson, MR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (24) :9103-9108
[3]   MPTP-INDUCED ATP LOSS IN MOUSE-BRAIN [J].
CHAN, P ;
DELANNEY, LE ;
IRWIN, I ;
LANGSTON, JW ;
DIMONTE, D .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1992, 648 :306-308
[4]   S-nitrosylation of Parkin regulates ubiquitination and compromises Parkin's protective function [J].
Chung, KKK ;
Thomas, B ;
Li, XJ ;
Pletnikova, O ;
Troncoso, JC ;
Marsh, L ;
Dawson, VL ;
Dawson, TM .
SCIENCE, 2004, 304 (5675) :1328-1331
[5]   Impaired degradation of mutant α-synuclein by chaperone-mediated autophagy [J].
Cuervo, AM ;
Stefanis, L ;
Fredenburg, R ;
Lansbury, PT ;
Sulzer, D .
SCIENCE, 2004, 305 (5688) :1292-1295
[6]   Parkinson's disease: Mechanisms and models [J].
Dauer, W ;
Przedborski, S .
NEURON, 2003, 39 (06) :889-909
[7]  
Fahn S, 2000, MERRITTS NEUROLOGY, P679
[8]   1-METHYL-4-PHENYLPYRIDINIUM (MPP+) INDUCES NADH-DEPENDENT SUPEROXIDE FORMATION AND ENHANCES NADH-DEPENDENT LIPID-PEROXIDATION IN BOVINE HEART SUBMITOCHONDRIAL PARTICLES [J].
HASEGAWA, E ;
TAKESHIGE, K ;
OISHI, T ;
MURAI, Y ;
MINAKAMI, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :1049-1055
[9]  
HASTINGS TG, 1995, J NEUROCHEM, V64, P919
[10]   MELANIZED DOPAMINERGIC-NEURONS ARE DIFFERENTIALLY SUSCEPTIBLE TO DEGENERATION IN PARKINSONS-DISEASE [J].
HIRSCH, E ;
GRAYBIEL, AM ;
AGID, YA .
NATURE, 1988, 334 (6180) :345-348