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Valproic Acid Regulates α-Synuclein Expression through JNK Pathway in Rat Primary Astrocytes

Although the role of α-synuclein aggregation on Parkinson’s disease is relatively well known, the physiological role and the regulatory mechanism governing the expression of α-synuclein are unclear yet. We recently reported that α-synuclein is expressed and secreted from cultured astrocytes. In this...

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Detalles Bibliográficos
Autores principales: Kim, Jung Nam, Kim, Min Kyeong, Cho, Kyu Suk, Choi, Chang Soon, Park, Seung Hwa, Yang, Sung-Il, Joo, So Hyun, Park, Jin Hee, Bahn, Geonho, Shin, Chan Young, Lee, He-Jin, Han, Seol-Heui, Kwon, Kyoung Ja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830121/
https://www.ncbi.nlm.nih.gov/pubmed/24265868
http://dx.doi.org/10.4062/biomolther.2013.006
Descripción
Sumario:Although the role of α-synuclein aggregation on Parkinson’s disease is relatively well known, the physiological role and the regulatory mechanism governing the expression of α-synuclein are unclear yet. We recently reported that α-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 α-synuclein in neuron, on α-synuclein expression in rat primary astrocytes. VPA concentrationdependently increased the protein expression level of α-synuclein in cultured rat primary astrocytes with concomitant increase in mRNA expression level. Likewise, the level of secreted α-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 α-synuclein. Whether the increased α-synuclein in astrocytes is involved in the reported neuroprotective effects of VPA awaits further investigation.