Cho Jun Hwi, Kim Dae Hyun, Lee Jong Suk, Seo Mi-Suk, Kim Mi Eun, Lee Jun Sik
Department of Life Science, Immunology Research Lab, BK21-Plus Research Team for Bioactive Control Technology, College of Natural Sciences, Chosun University, Dong-gu, Gwangju 61452, Korea.
Biocenter, Gyeonggido Business & Science Accelerator (GBSA), Suwon 16229, Gyeonggi-do, Korea.
Curr Issues Mol Biol. 2022 Nov 3;44(11):5416-5426. doi: 10.3390/cimb44110367.
Previously, we reported that () is a brown algae species that exerts anti-inflammatory activity toward murine macrophages. However, the anti-neuroinflammatory effects and the mechanism of on microglia cells are still unknown. We investigated the anti-neuroinflammatory effects of extract on microglia in vitro and in vivo. In the present study, we found that was not cytotoxic to BV-2 microglia cells and it significantly decreased lipopolysaccharide (LPS)-induced NO production. Moreover, also diminished the protein expression of iNOS, COX-2, and cytokine production, including IL-1β, TNF-α, and IL-6, on LPS-stimulated microglia activation. elicited anti-neuroinflammatory effects by inhibiting phosphorylation of p38 MAPK and NF-κB. In addition, inhibited astrocytes and microglia activation in LPS-challenged mice brain. Therefore, these results suggested that exerted anti-neuroinflammatory effects on LPS-stimulated microglia cell activation by inhibiting neuroinflammatory factors and NF-κB signaling.
此前,我们报道过()是一种对小鼠巨噬细胞具有抗炎活性的褐藻物种。然而,(该褐藻物种)对小胶质细胞的抗神经炎症作用及其机制仍不清楚。我们研究了(该褐藻物种)提取物在体外和体内对小胶质细胞的抗神经炎症作用。在本研究中,我们发现(该褐藻物种提取物)对BV - 2小胶质细胞无细胞毒性,且能显著降低脂多糖(LPS)诱导的一氧化氮(NO)生成。此外,(该褐藻物种提取物)还能减少LPS刺激的小胶质细胞活化过程中诱导型一氧化氮合酶(iNOS)、环氧化酶 - 2(COX - 2)的蛋白表达以及细胞因子的产生,包括白细胞介素 - 1β(IL - 1β)、肿瘤坏死因子 - α(TNF - α)和白细胞介素 - 6(IL - 6)。(该褐藻物种提取物)通过抑制p38丝裂原活化蛋白激酶(p38 MAPK)和核因子κB(NF - κB)的磷酸化发挥抗神经炎症作用。此外,(该褐藻物种提取物)抑制了LPS刺激的小鼠脑内星形胶质细胞和小胶质细胞的活化。因此,这些结果表明(该褐藻物种提取物)通过抑制神经炎症因子和NF - κB信号传导,对LPS刺激的小胶质细胞活化发挥抗神经炎症作用。