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Resolvin D1 and E1 promote resolution of inflammation in microglial cells in vitro

机译:Resolvin D1和E1促进体外小胶质细胞炎症的消退

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Sustained inflammation in the brain together with microglia activation can lead to neuronal damage. Hence limiting brain inflammation and activation of microglia is a real therapeutic strategy for inflammatory disease. Resolvin D1 (RvD1) and resolvin El (RvE1) derived from n-3 long chain polyunsaturated fatty acids are promising therapeutic compounds since they actively turn off the systemic inflammatory response. We thus evaluated the anti-inflammatory activities of RvD1 and RvE1 in microglia cells in vitro. BV2 cells were pre-incubated with RvD1 or RvE1 before lipopolysaccharide (LPS) treatment. RvD1 and RvE1 both decreased LPS-induced proinflammatory cytokines (TNF-alpha, IL-6 and IL-1 beta) gene expression, suggesting their proresolutive activity in microglia. However, the mechanisms involved are distinct as RvE1 regulates NF kappa B signaling pathway and RvD1 regulates miRNAs expression. Overall, our findings support that pro-resolving lipids are involved in the resolution of brain inflammation and can be considered as promising therapeutic agents for brain inflammation. (C) 2015 Elsevier Inc. All rights reserved.
机译:大脑中持续的炎症以及小胶质细胞的活化会导致神经元损伤。因此,限制脑部炎症和小胶质细胞的激活是炎症性疾病的真正治疗策略。衍生自n-3个长链多不饱和脂肪酸的Resolvin D1(RvD1)和Resolvin El(RvE1)是有前途的治疗化合物,因为它们会主动关闭全身炎症反应。因此,我们在体外评估了小胶质细胞中RvD1和RvE1的抗炎活性。在脂多糖(LPS)处理之前,将BV2细胞与RvD1或RvE1预孵育。 RvD1和RvE1均降低LPS诱导的促炎细胞因子(TNF-α,IL-6和IL-1 beta)基因表达,表明它们在小胶质细胞中具有前溶活性。但是,所涉及的机制是截然不同的,因为RvE1调节NFκB信号通路,而RvD1调节miRNA的表达。总体而言,我们的研究结果支持促脂类药物参与解决脑部炎症,可以被认为是治疗脑部炎症的有前途的治疗剂。 (C)2015 Elsevier Inc.保留所有权利。

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