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Oral Exposure to Paraquat Triggers Earlier Expression of Phosphorylated ?-Synuclein in the Enteric Nervous System of A53T Mutant Human ?-Synuclein Transgenic Mice.


ABSTRACT: The misfolded ?-synuclein protein, phosphorylated at serine 129 (pSer129 ?-syn), is the hallmark of Parkinson disease (PD). Detected also in the enteric nervous system (ENS), it supports the recent theory that PD could start in the gut, rather than the brain. In a previous study, using a transgenic mouse model of human synucleinopathies expressing the A53T mutant ?-synuclein (TgM83), in which a neurodegenerative process associated with ?-synuclein occurs spontaneously in the brain, we have shown earlier onset of pSer129 ?-syn in the ENS. Here, we used this model to study the impact of paraquat (PQ) a neurotoxic herbicide incriminated in PD in agricultural workers) on the enteric pSer129 ?-syn expression in young mice. Orally delivered in the drinking water at 10?mg/kg/day for 6-8?weeks, the impact of PQ was measured in a time-dependent manner on weight, locomotor abilities, pSer129 ?-syn, and glial fibrillary acidic protein (GFAP) expression levels in the ENS. Remarkably, pSer129 ?-syn was detected in ENS earlier under PQ oral exposure and enteric GFAP expression was also increased. These findings bring additional support to the theory that neurotoxic agents such as PQ initiate idiopathic PD after oral delivery.

SUBMITTER: Naudet N 

PROVIDER: S-EPMC5939863 | biostudies-other | 2017 Dec

REPOSITORIES: biostudies-other

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Oral Exposure to Paraquat Triggers Earlier Expression of Phosphorylated α-Synuclein in the Enteric Nervous System of A53T Mutant Human α-Synuclein Transgenic Mice.

Naudet Nicolas N   Antier Emilie E   Gaillard Damien D   Morignat Eric E   Lakhdar Latifa L   Baron Thierry T   Bencsik Anna A  

Journal of neuropathology and experimental neurology 20171201 12


The misfolded α-synuclein protein, phosphorylated at serine 129 (pSer129 α-syn), is the hallmark of Parkinson disease (PD). Detected also in the enteric nervous system (ENS), it supports the recent theory that PD could start in the gut, rather than the brain. In a previous study, using a transgenic mouse model of human synucleinopathies expressing the A53T mutant α-synuclein (TgM83), in which a neurodegenerative process associated with α-synuclein occurs spontaneously in the brain, we have shown  ...[more]

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