Paraquat and Parkinson's disease

被引:211
|
作者
Berry, C. [2 ]
La Vecchia, C. [3 ,4 ]
Nicotera, P. [1 ]
机构
[1] Deutsch Zentrum Neurodegenerat Erkrankungen, D-53175 Bonn, Germany
[2] Univ London, London E1 4NS, England
[3] Ist Richerche Farmacol Mario Negri, I-20156 Milan, Italy
[4] Univ Milan, Ist Stat Med Biometria, I-20133 Milan, Italy
来源
CELL DEATH AND DIFFERENTIATION | 2010年 / 17卷 / 07期
关键词
neurodegeneration; pesticides; parkinsonism; neurons; microglia; ENVIRONMENTAL RISK-FACTORS; REQUIRING PROLONGED OBSERVATION; NEURONAL CELL-DEATH; ALPHA-SYNUCLEIN; OXIDATIVE STRESS; HERBICIDE PARAQUAT; PESTICIDE EXPOSURE; COMPLEX-I; TOXICITY; DESIGN;
D O I
10.1038/cdd.2009.217
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As evidence emerges that complex gene alterations are involved in the onset of Parkinson's disease (PD), the role of environmental chemicals in the pathogenesis of this disease becomes intensely debated. Although it is undisputed that acute exposure to certain chemicals such as 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is sufficient to cause human parkinsonism, the evidence that the risk for PD increases because of environmental exposure is generally weaker. Several studies have suggested that pesticide exposure and life in rural areas are significant risks factors for PD. Among other pesticides, paraquat (PQ) has been linked to PD by epidemiological studies and experimental work in rodents, in which it causes lesions in the substantia nigra, pars compacta. However, the evidence that human exposure to the chemical results in an increased risk for PD is rather limited and based on insufficient epidemiological data. This review critically analyses the evidence that implicates PQ in parkinsonism and discusses the limitations of chemical modelling of PD. Cell Death and Differentiation (2010) 17, 1115-1125; doi:10.1038/cdd.2009.217; published online 22 January 2010
引用
收藏
页码:1115 / 1125
页数:11
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