Institute of Biochemistry and Molecular Biology, National Yang-Ming University, No.155, Sec.2, Linong Street, Taipei, 11221 Taiwan, ROC.
Int Immunopharmacol. 2011 Dec;11(12):2159-66. doi: 10.1016/j.intimp.2011.09.013. Epub 2011 Oct 11.
Many different kinds of fermented food are consumed daily in Taiwan, such as stinky tofu, suan-tsai, and fu-tsai. We have previously reported the diversity of lactic acid bacteria (LAB) at different stages of fermentation in the production of suan-tsai and fu-tsai. In this study, the anti-inflammatory and immunomodulatory activities of Lactobacillus plantarum K68 (K68) isolated from fu-tsai were evaluated. K68 significantly inhibited the production of tumor necrosis factor-α (TNF-α) and prostaglandin E(2) (PGE(2)) in lipopolysaccharide (LPS)-induced murine macrophage RAW 264.7 cells and stimulated interferon-γ (IFN-γ) production in human peripheral blood mononuclear cells (hPBMCs). Additionally, orally administered K68 ameliorated dextran sulfate sodium (DSS)-induced ulcerative colitis (UC) in BALB/c mice. Both the disease activity index (DAI) and histological scores (HIS) showed that the severity of UC was significantly reduced by oral administration of K68. Furthermore, the production of pro inflammatory cytokines TNF-α, interleukin-1β (IL-1β), and interleukin-6 (IL-6) was significantly reduced in K68-administered group. Colonic mRNA expression levels of TNF-α, cyclooxygenase-2 (COX-2), forkhead box P3 (Foxp3), suppressors of cytokine signaling 3 (SOCS3), and toll like receptor 4 (TLR4), were also reduced in the K68-administered group. These results suggest that K68 exhibits anti-inflammatory and immunomodulatory activities that ameliorate DSS-induced experimental colitis.
台湾地区民众日常食用的发酵食品种类繁多,如臭豆腐、酸菜、福菜等。我们之前的研究报告了酸菜和福菜发酵过程中不同阶段的乳酸菌(LAB)多样性。在这项研究中,我们评估了从福菜中分离出的植物乳杆菌 K68(K68)的抗炎和免疫调节活性。K68 显著抑制脂多糖(LPS)诱导的鼠源巨噬细胞 RAW 264.7 细胞中肿瘤坏死因子-α(TNF-α)和前列腺素 E(PGE(2))的产生,并刺激人外周血单核细胞(hPBMCs)中干扰素-γ(IFN-γ)的产生。此外,口服 K68 可改善葡聚糖硫酸钠(DSS)诱导的 BALB/c 小鼠溃疡性结肠炎(UC)。疾病活动指数(DAI)和组织学评分(HIS)均表明,口服 K68 可显著减轻 UC 的严重程度。此外,在 K68 给药组中,促炎细胞因子 TNF-α、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的产生也显著减少。K68 给药组结肠 TNF-α、环氧化酶-2(COX-2)、叉头框 P3(Foxp3)、细胞因子信号转导抑制因子 3(SOCS3)和 Toll 样受体 4(TLR4)的 mRNA 表达水平也降低。这些结果表明,K68 具有抗炎和免疫调节活性,可改善 DSS 诱导的实验性结肠炎。