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Tetracycline Inhibits Local Inflammation Induced by Cerebral Ischemia via Modulating Autophagy

BACKGROUND: Tetracycline exerts neuroprotection via suppressing the local inflammation induced by cerebral ischemia. However, the underlying mechanism is not completely clear. METHODOLOGY/PRINCIPAL FINDINGS: The mRNA and protein expressions of tumor necrosis factor α and interleukin 6 and the number...

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Detalles Bibliográficos
Autores principales: Jiang, Yongjun, Zhu, Juehua, Wu, Li, Xu, Gelin, Dai, Jianwu, Liu, Xinfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492486/
https://www.ncbi.nlm.nih.gov/pubmed/23144925
http://dx.doi.org/10.1371/journal.pone.0048672
Descripción
Sumario:BACKGROUND: Tetracycline exerts neuroprotection via suppressing the local inflammation induced by cerebral ischemia. However, the underlying mechanism is not completely clear. METHODOLOGY/PRINCIPAL FINDINGS: The mRNA and protein expressions of tumor necrosis factor α and interleukin 6 and the number of activated microglia were measured to detect the inflammatory process in the ischemic hemisphere. The key proteins of nuclear factor kappa B pathway and the binding activity of nuclear factor kappa B were also measured. Two key components of autophagy, Beclin 1 and LC3, were detected by western blotting. Pretreatment with tetracycline inhibited the mRNA and protein expressions of tumor necrosis factor α and interleukin 6 and decreased the numbers of activated and phagocytotic microglia. Tetracycline down regulated the total and phosphorylated expressions of IKK, IκB and p65 (P<0.05). The autophagy inhibitor, 3-methyladenine, inhibited inflammation and activation of nuclear factor kappa B pathway. The levels of Beclin 1 and LC3 were decreased by 3-methyladenine and tetracycline. CONCLUSIONS/SIGNIFICANCE: Our data suggested that pretreatment of tetracycline may inhibit autophagy in the ischemic stroke brain and then suppress the inflammatory process via inhibiting the activation of nuclear factor kappa B pathway.