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Long non-coding RNA BC168687 small interfering RNA reduces high glucose and high free fatty acid-induced expression of P2X(7) receptors in satellite glial cells

Purinergic signaling contributes to inflammatory and immune responses. The activation of the P2X purinoceptor 7 (P2X(7)) in satellite glial cells (SGCs) may be an essential component in the promotion of inflammation and neuropathic pain. Long non-coding RNAs (lncRNAs) are involved in multiple physio...

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Detalles Bibliográficos
Autores principales: Liu, Cheng-Long, Deng, Ze-Yu, Du, Er-Rong, Xu, Chang-Shui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866030/
https://www.ncbi.nlm.nih.gov/pubmed/29436679
http://dx.doi.org/10.3892/mmr.2018.8601
Descripción
Sumario:Purinergic signaling contributes to inflammatory and immune responses. The activation of the P2X purinoceptor 7 (P2X(7)) in satellite glial cells (SGCs) may be an essential component in the promotion of inflammation and neuropathic pain. Long non-coding RNAs (lncRNAs) are involved in multiple physiological and pathological processes. The aim of the present study was to investigate the effects of a small interfering RNA for the lncRNA BC168687 on SGC P2X(7) expression in a high glucose and high free fatty acids (HGHF) environment. It was demonstrated that BC168687 small interfering (si)RNA downregulated the co-expression of the P2X(7) and glial fibrillary acidic protein and P2X(7) mRNA expression. Additionally, HGHF may activate the mitogen-activated protein kinase signaling pathway by increasing the release of nitric oxide and reactive oxygen species in SGCs. Taken together, these results indicate that silencing BC168687 expression may downregulate the increased expression of P2X(7) receptors in SGCs induced by a HGHF environment.