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地塞米松可预防实验性细菌性脑膜炎共培养模型中 LPS 诱导的小胶质细胞激活和星形胶质细胞损伤。

Dexamethasone prevents LPS-induced microglial activation and astroglial impairment in an experimental bacterial meningitis co-culture model.

机构信息

Department of Neuroanatomy and Molecular Brain Research, Ruhr- University Bochum, Universitätsstrasse 150, 44780 Bochum, Germany.

出版信息

Brain Res. 2010 May 6;1329:45-54. doi: 10.1016/j.brainres.2010.03.012. Epub 2010 Mar 15.

Abstract

We analyzed the effect of dexamethasone on gram-negative bacteria derived lipopolysaccharide (LPS) induced inflammation in astroglial/microglial co-cultures. At the cellular level the microglial phenotype converted to an activated type after LPS incubation. Furthermore, LPS compromised functional astroglial properties like membrane resting potential, intracellular coupling and connexin 43 (Cx43) expression. This change in Cx43 expression was not due to a downregulation of Cx43 mRNA expression. Morphological and functional changes were accompanied by a time-dependent release of inflammation related cytokines. Co-incubation of dexamethasone with LPS prevented these LPS-induced changes within our glial co-culture model. The ability of dexamethasone to reconstitute astrocytic properties and to decrease microglial activation in vitro could be one possible explanation for the beneficial effects of dexamethasone in the treatment of acute bacterial meningitis in vivo.

摘要

我们分析了地塞米松对星形胶质细胞/小胶质细胞共培养物中革兰氏阴性菌来源的脂多糖 (LPS) 诱导炎症的影响。在细胞水平上,LPS 孵育后小胶质细胞表型转化为激活型。此外,LPS 损害了功能性星形胶质细胞的特性,如膜静息电位、细胞内偶联和连接蛋白 43 (Cx43) 的表达。Cx43 表达的这种变化不是由于 Cx43 mRNA 表达的下调。形态和功能的变化伴随着与炎症相关细胞因子的时间依赖性释放。地塞米松与 LPS 共同孵育可防止我们的神经胶质细胞共培养模型中发生这些 LPS 诱导的变化。地塞米松在体外重建星形胶质细胞特性和减少小胶质细胞激活的能力可能是地塞米松在治疗体内急性细菌性脑膜炎方面有益作用的一个可能解释。

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