a School of Allied Health Sciences , Walailak University , Nakhon Si Thammarat , Thailand.
b Department of Chemistry, School of Science , University of Phayao , Phayao , Thailand.
Immunopharmacol Immunotoxicol. 2018 Feb;40(1):43-51. doi: 10.1080/08923973.2017.1405437. Epub 2017 Dec 4.
Immune dysregulation has been implicated in the pathogenesis of many diseases. Macrophages play a crucial role contributing to the onset, progression, and resolution of inflammation. Macrophage inflammatory mediators are of considerable interest as potential targets to treat inflammatory diseases.
The present study was conducted to elucidate the anti-inflammatory mechanism of 2',4-dihydroxy-3',4',6'-trimethoxychalcone (1), the major chalcone isolated from Chromolaena odorata (L.) R.M.King & H.Rob, against lipopolysaccharide (LPS)-induced inflammation in RAW 264.7 macrophages.
Cell viability, nitric oxide (NO), and proinflammatory cytokines of LPS-activated RAW 264.7 cells were measured by MTT, Griess, and ELISA assays, respectively. Cell lysates were subjected to Western blotting for investigation of protein expression.
Treatment with the major chalcone 1 significantly attenuated the production of NO and proinflammatory cytokines, tumor necrosis factor-α, interleukin-1β, and interleukin-6 in a dose-dependent manner. The chalcone suppressed nuclear factor-κB (NF-κB) stimulation by preventing activation of inhibitor κB kinase (IKK) α/β, degradation of inhibitor κB (IκB) α, and translocation of p65 NF-κB into the nucleus. Additionally, the chalcone markedly repressed the phosphorylation of p38 mitogen-activated protein kinase (MAPK), but no further inhibition was detected for c-Jun N-terminal activated kinases or extracellular regulated kinases. Thus, suppression of NF-κB and p38 MAPK activation may be the core mechanism underlying the anti-inflammatory activity of 2',4-dihydroxy-3',4',6'-trimethoxychalcone (1).
These findings provide evidence that 2',4-dihydroxy-3',4',6'-trimethoxychalcone (1) possesses anti-inflammatory activity via targeting proinflammatory macrophages. This anti-inflammatory chalcone is a promising compound for reducing inflammation.
免疫失调与许多疾病的发病机制有关。巨噬细胞在炎症的发生、发展和消退中起着至关重要的作用。巨噬细胞炎症介质是治疗炎症性疾病的潜在靶点,具有重要意义。
本研究旨在阐明从 Chromolaena odorata (L.) R.M.King & H.Rob 中分离得到的主要查尔酮 2',4-二羟基-3',4',6'-三甲氧基查尔酮(1)对脂多糖(LPS)诱导的 RAW 264.7 巨噬细胞炎症的抗炎机制。
通过 MTT、Griess 和 ELISA 测定分别测定细胞活力、一氧化氮(NO)和 LPS 激活的 RAW 264.7 细胞中的促炎细胞因子。细胞裂解物进行 Western 印迹分析以研究蛋白表达。
用主要查尔酮 1 处理可显著抑制 NO 和促炎细胞因子(肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6)的产生,呈剂量依赖性。该查尔酮通过抑制 IκB 激酶(IKK)α/β 的激活、IκBα 的降解和 p65 NF-κB 向核内转位来抑制核因子-κB(NF-κB)的刺激。此外,查尔酮还显著抑制 p38 丝裂原活化蛋白激酶(MAPK)的磷酸化,但对 c-Jun N 端激活激酶或细胞外调节激酶没有进一步抑制作用。因此,抑制 NF-κB 和 p38 MAPK 的激活可能是 2',4-二羟基-3',4',6'-三甲氧基查尔酮(1)抗炎活性的核心机制。
这些发现为 2',4-二羟基-3',4',6'-三甲氧基查尔酮(1)通过靶向促炎巨噬细胞发挥抗炎活性提供了证据。这种抗炎查尔酮是减少炎症的有前途的化合物。