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Valproic Acid Regulates alpha-Synuclein Expression through JNK Pathway in Rat Primary Astrocytes
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-202360
Biblioteca responsável: WPRO
ABSTRACT
Although the role of alpha-synuclein aggregation on Parkinson's disease is relatively well known, the physiological role and the regulatory mechanism governing the expression of alpha-synuclein are unclear yet. We recently reported that alpha-synuclein is expressed and secreted from cultured astrocytes. In this study, we investigated the effect of valproic acid (VPA), which has been suggested to provide neuroprotection by increasing alpha-synuclein in neuron, on alpha-synuclein expression in rat primary astrocytes. VPA concentration-dependently increased the protein expression level of alpha-synuclein in cultured rat primary astrocytes with concomitant increase in mRNA expression level. Likewise, the level of secreted alpha-synuclein was also increased by VPA. VPA increased the phosphorylation of Erk1/2 and JNK and pretreatment of a JNK inhibitor SP600125 prevented the VPA-induced increase in alpha-synuclein. Whether the increased alpha-synuclein in astrocytes is involved in the reported neuroprotective effects of VPA awaits further investigation.
Assuntos

Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Doença de Parkinson / Fosforilação / Acetilação / RNA Mensageiro / Astrócitos / Ácido Valproico / Fármacos Neuroprotetores / Sistema de Sinalização das MAP Quinases / Alfa-Sinucleína / Neurônios Limite: Animais Idioma: Inglês Revista: Biomolecules & Therapeutics Ano de publicação: 2013 Tipo de documento: Artigo
Texto completo: Disponível Base de dados: WPRIM (Pacífico Ocidental) Assunto principal: Doença de Parkinson / Fosforilação / Acetilação / RNA Mensageiro / Astrócitos / Ácido Valproico / Fármacos Neuroprotetores / Sistema de Sinalização das MAP Quinases / Alfa-Sinucleína / Neurônios Limite: Animais Idioma: Inglês Revista: Biomolecules & Therapeutics Ano de publicação: 2013 Tipo de documento: Artigo
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