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Betulinic Acid Inhibits Lps-Induced Mmp-9 Expression by Suppressing Nf-Kb Activation in Bv2 Microglial Cells

机译:通过抑制BV2微胶质细胞中的NF-KB活化,桦木酸抑制LPS诱导的MMP-9表达

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The objective of the present study was to evaluate anti-inflammatory effects of betulinic acid on lipopolysaccharide (LPS)-stimulated BV2 microglial cells. Pretreatment of betulinic acid significantly attenuated LPS-induced NO production and protein expression of iNOS. Betulinic acid also significantly suppressed LPS-induced release and expression of cytokines such as TNF-oc and IL-1β. Furthermore, betulinic acid significantly suppressed LPS-induced MMP-9 expression, which has been suggested to play an important role in the migration of activated microglia. In order to understand the possible mechanism by which betulinic acid suppresses LPS-induced cytokine production and migration of microglia, the role of NF-kB, a major proinflammatory transcription factor, was examined. Betulinic acid significantly suppressed LPS-induced degradation of IkB, which retains NF-kB in the cytoplasm. Therefore, nuclear translocation of NF-kB upon LPS stimulation was significantly suppressed bybetulinic acid. Taken together, the present study for the first time demonstrates thatbetulinic acid possesses anti-inflammatory activity and inhibition of microglial migration through the suppression of nuclear translocation of NF-kB in BV2 microglial cells.
机译:本研究的目的是评估桦木酸对脂多糖(LPS)刺激的B​​V2微胶质细胞的抗炎作用。预处理桦木酸显着减弱LPS诱导的NO inos的生产和蛋白质表达。桦木酸也显着抑制了LPS诱导的释放和细胞因子的表达,例如TNF-OC和IL-1β。此外,桦木酸显着抑制了LPS诱导的MMP-9表达,这提出了在活化的微胶质植物的迁移中起重要作用。为了了解桦木酸抑制LPS诱导的细胞因子产生和微胶质细胞迁移的可能机制,检查了NF-KB的作用,主要的促炎症转录因子。桦木酸显着抑制IKB的LPS诱导的降解,其在细胞质中保留NF-KB。因此,NF-KB对LPS刺激的核转位显着抑制百乙酸。在一起,本研究首次证明了通过抑制BV2微胶质细胞NF-KB的核易位具有抗炎酸具有抗炎活性和微胶质迁移的抑制。

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