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Acute meningitis in rats is associated with decreased levels of miR132 and miR146a

INTRODUCTION: The pathogenesis of bacterial meningitis due to Streptococcus pneumoniae is still unclear. Despite early treatment with antibiotics, its morbidity and mortality is still high. MATERIAL AND METHODS: Streptococcus pneumoniae induced rat meningitis models were taken and divided into 2 gro...

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Detalles Bibliográficos
Autores principales: Jagoo, Mubareka, He, Fang, Peng, Jing, Yin, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439992/
https://www.ncbi.nlm.nih.gov/pubmed/26155141
http://dx.doi.org/10.5114/ceji.2014.45941
Descripción
Sumario:INTRODUCTION: The pathogenesis of bacterial meningitis due to Streptococcus pneumoniae is still unclear. Despite early treatment with antibiotics, its morbidity and mortality is still high. MATERIAL AND METHODS: Streptococcus pneumoniae induced rat meningitis models were taken and divided into 2 groups; control (C) and meningitis (M). Western blot was used to detect toll like receptor 4 (TLR4), tumor necrosis factor α (TNF-α), interleukin 1B (IL1B), nuclear factor κB (NFκB) and real time polymerase chain reaction were used to detect the expression of miR146a, miR132, respectively. RESULTS: We found that the expressions of TLR4, TNF-α, IL1B, NFκB were all up-regulated in the acute stage of bacterial meningitis when compared to the control group. While for the post transcription factors, miR146a and miR132, the opposite was observed. They were down-regulated in the meningitis group. CONCLUSIONS: miR146a and miR132 may take part in the pathogenesis of SP bacterial meningitis as well as the TLR4- NFκB- TNF-α/IL1B signal transduction pathway.