Ishida Momoko, Takekuni Chihiro, Nishi Kosuke, Sugahara Takuya
Graduate School of Agriculture, Ehime University, 3-5-7 Tarumi, Matsuyama, Ehime, 790-8566, Japan.
Food and Health Sciences Research Center, Ehime University, Matsuyama, Ehime, 790-8566, Japan.
Cytotechnology. 2019 Jun 12;71(4):797-807. doi: 10.1007/s10616-019-00323-4.
Kawachi-bankan (Citrus maxima) is one of the citruses produced in Ehime, Japan. Although health functions of flavonoids and carotenoids in citrus peel have been studied very well, those of water-soluble substances in the peel have not been focused. We herein indicated the anti-inflammatory effect of Kawachi-bankan peel aqueous extract (KPE) in vitro and in vivo. KPE significantly inhibited the production of inflammatory cytokines such as interleukin (IL)-6 and tumor necrosis factor (TNF)-α by LPS-stimulated RAW264.7 cells without cytotoxicity. KPE also significantly inhibited the mRNA expression levels of IL-6 and TNF-α in the cells, suggesting that KPE inhibits the production of inflammatory cytokines by suppressing the gene expression levels. Immunoblot analysis revealed that KPE shows an anti-inflammatory effect on macrophages through the suppression of the phosphorylation of p38 and the translocation of NF-κB into nucleus. The oral administration of KPE inhibited the serum levels of inflammatory cytokines and improved the survival rate in systemic inflammatory response syndrome (SIRS) model mice. Our experiments using a cell line suggested that KPE inhibits the production of inflammatory cytokines by macrophages in hyperinflammatory state. In addition, experiments in vivo showed that the oral administration of KPE inhibited the serum levels of inflammatory cytokines and improved the survival rate in SIRS model mice. Our findings indicated that KPE contributes to alleviating of a hyperinflammatory response.
河内文旦(Citrus maxima)是日本爱媛县产的柑橘之一。尽管柑橘皮中黄酮类化合物和类胡萝卜素的健康功能已得到充分研究,但果皮中水溶性物质的健康功能尚未受到关注。我们在此指出了河内文旦皮水提取物(KPE)在体外和体内的抗炎作用。KPE显著抑制脂多糖刺激的RAW264.7细胞产生炎性细胞因子,如白细胞介素(IL)-6和肿瘤坏死因子(TNF)-α,且无细胞毒性。KPE还显著抑制细胞中IL-6和TNF-α的mRNA表达水平,表明KPE通过抑制基因表达水平来抑制炎性细胞因子的产生。免疫印迹分析显示,KPE通过抑制p38磷酸化和NF-κB向细胞核的转位,对巨噬细胞发挥抗炎作用。口服KPE可抑制全身炎症反应综合征(SIRS)模型小鼠血清中炎性细胞因子水平,并提高其存活率。我们使用细胞系进行的实验表明,KPE可抑制处于高炎症状态的巨噬细胞产生炎性细胞因子。此外,体内实验表明,口服KPE可抑制SIRS模型小鼠血清中炎性细胞因子水平,并提高其存活率。我们的研究结果表明,KPE有助于减轻高炎症反应。