Department of Molecular Medicine and Tissue Injury Defense Research Center, Ewha Womans University Medical School, Mok-6-dong 911-1, Yangchun-Ku, Seoul, 158-710, South Korea.
Department of Life and Nanopharmaceutical Sciences, College of Pharmacy, Kyung Hee University, Seoul, Republic of Korea.
J Neuroimmune Pharmacol. 2016 Jun;11(2):294-305. doi: 10.1007/s11481-016-9657-x. Epub 2016 Feb 22.
Tangeretin, a flavonoid from citrus fruit peels, has been proven to play an important role in anti-inflammatory responses and neuroprotective effects in several disease models, but further study is necessary for elucidating the detailed mechanisms of these effects. In this study, we examined the anti-inflammatory effect of tangeretin in lipopolysaccharide (LPS)-stimulated microglia. We first observed that tangeretin inhibited LPS-induced production of nitric oxide, tumor necrosis factor alpha, interleukin (IL)-6, and IL-1β, as well as LPS-induced mRNA expression of inducible nitric oxide synthases and cytokines. Additionally, we found that the activities, mRNA levels, and protein levels of matrix metalloproteinase (MMP)-3 and MMP-8 were inhibited, while the expression of tissue inhibitor of metalloproteinase-2 was enhanced by tangeretin in LPS-stimulated microglia. Further mechanistic study showed that tangeretin suppressed LPS-induced phosphorylation of mitogen-activated protein kinases and Akt. Also, tangeretin inhibited nuclear factor-κB by upregulating sirtuin 1 and 5'-adenosine monophosphate-activated protein kinase. We further demonstrated the antioxidant effect of tangeretin by showing that tangeretin inhibited reactive oxygen species production and p47(phox) phosphorylation, while enhancing the expression of heme oxygenase-1 and the DNA binding activity of nuclear factor-erythroid 2-related factor 2 to the antioxidant response element in LPS-stimulated microglia. Taken together, the results of the present study demonstrate that tangeretin possesses a potent anti-inflammatory and antioxidant effect in microglia.
蜜橘素是一种存在于柑橘类果皮中的类黄酮,已被证明在几种疾病模型中具有抗炎反应和神经保护作用,但为了阐明这些作用的详细机制,还需要进一步研究。在这项研究中,我们研究了蜜橘素对脂多糖(LPS)刺激的小胶质细胞的抗炎作用。我们首先观察到,蜜橘素抑制了 LPS 诱导的一氧化氮、肿瘤坏死因子-α、白细胞介素(IL)-6 和 IL-1β的产生,以及 LPS 诱导的诱导型一氧化氮合酶和细胞因子的 mRNA 表达。此外,我们发现,蜜橘素抑制了 LPS 刺激的小胶质细胞中基质金属蛋白酶(MMP)-3 和 MMP-8 的活性、mRNA 水平和蛋白水平,同时增强了组织金属蛋白酶抑制剂-2 的表达。进一步的机制研究表明,蜜橘素通过抑制丝裂原活化蛋白激酶和 Akt 的磷酸化来抑制 LPS 诱导的核因子-κB。此外,蜜橘素通过上调 Sirtuin 1 和 5'-单磷酸腺苷激活蛋白激酶来抑制核因子-κB。我们通过显示蜜橘素抑制活性氧物种的产生和 p47(phox)磷酸化,同时增强血红素加氧酶-1 的表达和核因子-红细胞 2 相关因子 2 到 LPS 刺激的小胶质细胞中抗氧化反应元件的 DNA 结合活性,进一步证明了蜜橘素的抗氧化作用。综上所述,本研究结果表明,蜜橘素在小胶质细胞中具有强大的抗炎和抗氧化作用。