Animal Models of Parkinson's Disease: Limits and Relevance to Neuroprotection Studies

被引:133
作者
Bezard, Erwan [1 ,2 ,3 ]
Yue, Zhenyu [4 ,5 ]
Kirik, Deniz [6 ]
Spillantini, Maria Grazia [7 ]
机构
[1] Univ Bordeaux, Inst Malad Neurodegenerat, UMR 5293, Bordeaux, France
[2] CNRS, Inst Malad Neurodegenerat, UMR 5293, Bordeaux, France
[3] Hop Pellegrin, Ctr Hosp Univ, Dept Clin Neurophysiol, F-33076 Bordeaux, France
[4] Mt Sinai Sch Med, Friedman Brain Inst, Dept Neurol, New York, NY USA
[5] Mt Sinai Sch Med, Friedman Brain Inst, Dept Neurosci, New York, NY USA
[6] Lund Univ, Dept Expt Med Sci, Brain Repair & Imaging Neural Syst Unit, Lund, Sweden
[7] Univ Cambridge, Dept Clin Neurosci, Cambridge Ctr Brain Repair, Cambridge, England
基金
瑞典研究理事会; 欧洲研究理事会; 美国国家卫生研究院;
关键词
6-OHDA; MPTP; alpha-synuclein; LRRK2; neurodegeneration; dopamine; viral vectors; HUMAN ALPHA-SYNUCLEIN; VECTOR-MEDIATED OVEREXPRESSION; NIGROSTRIATAL DOPAMINE SYSTEM; TRANSGENIC MOUSE MODEL; SUBSTANTIA-NIGRA; LEWY BODIES; RAT MODEL; MICE LACKING; STRIATAL DOPAMINE; CLINICAL-TRIALS;
D O I
10.1002/mds.25108
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Over the last two decades, significant strides has been made toward acquiring a better knowledge of both the etiology and pathogenesis of Parkinson's disease (PD). Experimental models are of paramount importance to obtain greater insights into the pathogenesis of the disease. Thus far, neurotoxin-based animal models have been the most popular tools employed to produce selective neuronal death in both in vitro and in vivo systems. These models have been commonly referred to as the pathogenic models. The current trend in modeling PD revolves around what can be called the disease gene-based models or etiologic models. The value of utilizing multiple models with a different mechanism of insult rests on the premise that dopamine-producing neurons die by stereotyped cascades that can be activated by a range of insults, from neurotoxins to downregulation and overexpression of disease-related genes. In this position article, we present the relevance of both pathogenic and etiologic models as well as the concept of clinically relevant designs that, we argue, should be utilized in the preclinical development phase of new neuroprotective therapies before embarking into clinical trials. (C) 2012 Movement Disorder Society
引用
收藏
页码:61 / 70
页数:10
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