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Inhibition of sPLA(2)-IIA Prevents LPS-Induced Neuroinflammation by Suppressing ERK1/2-cPLA(2)α Pathway in Mice Cerebral Cortex

Neuroinflammation is involved in various central nervous system (CNS) disorders, including brain infections, ischemia, trauma, stroke, and degenerative CNS diseases. In the CNS inflammation, secretory phospholipase A(2)-IIA (sPLA(2)-IIA) acts as a mediator, resulting in the generation of the precurs...

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Detalles Bibliográficos
Autores principales: Xiang, Yanxiao, Chen, Lin, Liu, Huiqing, Liu, Xiaoqian, Wei, Xinbing, Sun, Baozhu, Wang, Tian, Zhang, Xiumei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793966/
https://www.ncbi.nlm.nih.gov/pubmed/24130900
http://dx.doi.org/10.1371/journal.pone.0077909
Descripción
Sumario:Neuroinflammation is involved in various central nervous system (CNS) disorders, including brain infections, ischemia, trauma, stroke, and degenerative CNS diseases. In the CNS inflammation, secretory phospholipase A(2)-IIA (sPLA(2)-IIA) acts as a mediator, resulting in the generation of the precursors of pro-inflammatory lipid mediators, such as prostaglandins (PGs) and leukotrienes (LTs). However, the role of sPLA(2)-IIA in neuroinflammation is more complicated and remains unclear yet. In the present study, we investigated the effect of sPLA(2)-IIA inhibition by specific inhibitor SC-215 on the inflammation in LPS-induced mice cerebral cortex and primary astrocytes. Our results showed that the inhibition of sPLA(2)-IIA alleviated the release of PGE(2) by suppressing the activation of ERK1/2, cPLA(2)α, COX-2 and mPGES-1. These findings demonstrated that sPLA(2)-IIA showed the potential to regulate the neuroinflammation in vivo and in vitro, indicating that sPLA(2)-IIA might be a novel target for the treatment of acute neuroinflammation.