Increased sensitivity to MPTP in human α-synuclein A30P transgenic mice

被引:77
作者
Nieto, María
Gil-Bea, Francisco J.
Dalfó, Esther
Cuadrado, Mar
Cabodevilla, Felipe
Sanchez, Belén
Catena, Silvia
Sesma, Teresa
Ribe, Elena
Ferrer, Isidro
Ramirez, María J.
Gomez-Isla, Teresa [1 ]
机构
[1] Univ Navarra, Dept Neurol & Neurosurg, Clin Univ Navarra, Navarra, Spain
[2] Univ Navarra, Dept Pharmacol, Navarra, Spain
[3] Bellvitge Hosp, Inst Neuropatol, Serv Anat Patol, Lhospitalet De Llobregat, Spain
[4] Univ Barcelona, Hosp Llobregat, Unitat Neuropatol Expt, Barcelona, Spain
关键词
MPTP; rotenone; synuclein; transgenic mice; Parkinson's disease; Lewy body; tyrosine hydroxylase; substantia nigra; dopamine;
D O I
10.1016/j.neurobiolaging.2005.04.010
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
In addition to genetic factors, environmental factors have long been suspected to contribute to the pathogenesis of Parkinson's disease (PD). We investigated the possible interaction between genetic factors and neurotoxins by testing whether alpha-synuclein A30P Tg5093 transgenic mice show increased sensitivity to secondary toxic insults like 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) or rotenone. While sensitivity to chronic treatment with rotenone was not enhanced in the Tg5093 line, chronic treatment with 80 or 150 mg/kg MPTP resulted in increased deterioration of the nigrostriatal dopaminergic system as assessed by quantitation of nigral tyrosine hydroxylase (TH) positive neurons and striatal dopamine (DA) levels in Tg5093 mice when compared to non-transgenic littermate controls. Thus, the results of this study demonstrate a role for the overexpression of mutant human a-synuclein A30P in increased vulneravility of DA neurons to MPTR (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:848 / 856
页数:9
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