Department of Biochemistry, School of Medicine, China Medical University, Taichung 40402, Taiwan.
Institute of Translational Medicine and New Drug Development, China Medical University, Taichung 40402, Taiwan.
Nutrients. 2022 Dec 19;14(24):5402. doi: 10.3390/nu14245402.
Macrophages and microglia are highly versatile cells that can be polarized into M1 and M2 phenotypes in response to diverse environmental stimuli, thus exhibiting different biological functions. In the central nervous system, activated resident macrophages and microglial cells trigger the production of proinflammatory mediators that contribute to neurodegenerative diseases and psychiatric disorders. Therefore, modulating the activation of macrophages and microglia by optimizing the inflammatory environment is beneficial for disease management. Several naturally occurring compounds have been reported to have anti-inflammatory and neuroprotective properties. Zerumbone is a phytochemical sesquiterpenoid and also a cyclic ketone isolated from Zingiber zerumbet Smith. In this study, we found that zerumbone effectively reduced the expression of lipocalin-2 in macrophages and microglial cell lines. Lipocalin-2, also known as neutrophil gelatinase-associated lipocalin (NGAL), has been characterized as an adipokine/cytokine implicated in inflammation. Moreover, supplement with zerumbone inhibited reactive oxygen species production. Phagocytic activity was decreased following the zerumbone supplement. In addition, the zerumbone supplement remarkably reduced the production of M1-polarization-associated chemokines CXC10 and CCL-2, as well as M1-polarization-associated cytokines interleukin (IL)-6, IL-1β, and tumor necrosis factor-α. Furthermore, the expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 and the production of NO were attenuated in macrophages and microglial cells supplemented with zerumbone. Notably, we discovered that zerumbone effectively promoted the production of the endogenous antioxidants heme oxygenase-1, glutamate-cysteine ligase modifier subunit, glutamate-cysteine ligase catalytic subunit, and NAD(P)H quinone oxidoreductase-1 and remarkably enhanced IL-10, a marker of M2 macrophage polarization. Endogenous antioxidant production and M2 macrophage polarization were increased through activation of the AMPK/Akt and Akt/GSK3 signaling pathways. In summary, this study demonstrated the protective role of zerumbone in maintaining M1 and M2 polarization homeostasis by decreasing inflammatory responses and enhancing the production of endogenous antioxidants in both macrophages and microglia cells. This study suggests that zerumbone can be used as a potential therapeutic drug for the supplement of neuroinflammatory diseases.
巨噬细胞和小胶质细胞是多功能细胞,它们可以在不同的环境刺激下极化成为 M1 和 M2 表型,从而表现出不同的生物学功能。在中枢神经系统中,激活的常驻巨噬细胞和小胶质细胞会触发促炎介质的产生,从而导致神经退行性疾病和精神障碍。因此,通过优化炎症环境来调节巨噬细胞和小胶质细胞的激活,有利于疾病的管理。一些天然存在的化合物具有抗炎和神经保护作用。生姜烯酮是一种植物化学倍半萜类化合物,也是从姜黄中分离出来的环状酮。在这项研究中,我们发现生姜烯酮能有效降低巨噬细胞和小胶质细胞系中脂联素-2 的表达。脂联素-2 也被称为中性粒细胞明胶酶相关脂质运载蛋白(NGAL),是一种被认为与炎症有关的脂肪细胞/细胞因子。此外,生姜烯酮的补充抑制了活性氧的产生。吞噬活性在补充生姜烯酮后下降。此外,生姜烯酮的补充显著降低了 M1 极化相关趋化因子 CXCL10 和 CCL-2 以及 M1 极化相关细胞因子白细胞介素(IL)-6、IL-1β 和肿瘤坏死因子-α的产生。此外,在补充生姜烯酮的巨噬细胞和小胶质细胞中,诱导型一氧化氮合酶(iNOS)和环氧化酶-2 的表达以及 NO 的产生均减弱。值得注意的是,我们发现生姜烯酮能有效地促进血红素加氧酶-1、谷胱甘肽半胱氨酸连接酶修饰亚基、谷胱甘肽半胱氨酸连接酶催化亚基和 NAD(P)H 醌氧化还原酶-1 的内源性抗氧化剂的产生,并显著增加了 IL-10,这是 M2 巨噬细胞极化的标志。通过激活 AMPK/Akt 和 Akt/GSK3 信号通路,增加了内源性抗氧化剂的产生和 M2 巨噬细胞极化。总之,这项研究表明,生姜烯酮通过降低炎症反应和增强巨噬细胞和小胶质细胞中内源性抗氧化剂的产生,在维持 M1 和 M2 极化平衡方面发挥了保护作用。这项研究表明,生姜烯酮可用作神经炎症性疾病补充治疗的潜在药物。