Agrochemicals, α-synuclein, and Parkinson's Disease

Document Type

Article

Publication Date

2013

Keywords

α-synuclein, Parkinson’s Disease, Environmental Toxin, Misfolding, Fibrillation, Intrinsically Disordered Protein, Pesticide, Agrochemical

Digital Object Identifier (DOI)

https://doi.org/10.1007/s12035-012-8333-2

Abstract

Epidemiological, population-based case-control, and experimental studies at the molecular, cellular, and organism levels revealed that exposure to various environmental agents, including a number of structurally different agrochemicals, may contribute to the pathogenesis of Parkinson's disease (PD) and several other neurodegenerative disorders. The role of genetic predisposition in PD has also been increasingly acknowledged, driven by the identification of a number of disease-related genes [e.g., α-synuclein, parkin, DJ-1, ubiquitin C-terminal hydrolase isozyme L1 (UCH-L1), and nuclear receptor-related factor 1]. Therefore, the etiology of this multifactorial disease is likely to involve both genetic and environmental factors. Various neurotoxicants, including agrochemicals, have been shown to elevate the levels of α-synuclein expression in neurons and to promote aggregation of this protein in vivo. Many agrochemicals physically interact with α-synuclein and accelerate the fibrillation and aggregation rates of this protein in vitro. This review analyzes some of the aspects linking α-synuclein to PD, provides brief structural and functional descriptions of this important protein, and represents some data connecting exposure to agrochemicals with α-synuclein aggregation and PD pathogenesis.

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Yes

Citation / Publisher Attribution

Molecular Neurobiology, v. 47, issue 2, p. 598-612

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