Organization of Advanced Science and Technology, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.
Int Immunopharmacol. 2009 Nov;9(12):1444-51. doi: 10.1016/j.intimp.2009.08.018. Epub 2009 Sep 5.
Probiotics have been used to treat human gastrointestinal inflammations including inflammatory bowel disease (IBD). However, the exact mechanisms by which probiotics act to protect against intestinal inflammation have yet to be fully elucidated. The aim of this study was to evaluate anti-inflammatory effects of Lactococcus lactis subsp. cremoris FC using in vivo and in vitro inflammation models. Colitis was induced in C57BL/6 mice by administration of 3% dextran sulfate sodium to drinking water. In the cellular level assessment, a gut inflammation model with the co-culture system consisting Caco-2 cells and RAW264.7 cells stimulated by LPS was used. Administration of L. lactis subsp. cremoris FC significantly ameliorated shortening of colon length and histological score of the colon in DSS-induce colitis mice. In addition, the treatment of L. lactis subsp. cremoris FC improved the aberrant mRNA expression in inflamed tissue near to control level through notable suppression of TNF-alpha (P<0.05), IFN-gamma (P<0.05), IL-6, iNOS, and MIP-2 mRNA expression. In addition, in a gut inflammation model, treatment with L. lactis subsp. cremoris FC resulted in significant down-regulation of IL-8 mRNA expression in Caco-2 cells and inhibition of NF-kappaB nuclear translocation in RAW264.7 cells. Our findings indicate that administration of L. lactis subsp. cremoris FC improves negative effects of DSS-induced colitis in mice through the inhibition of inflammatory cell infiltration.
益生菌已被用于治疗人类胃肠道炎症,包括炎症性肠病(IBD)。然而,益生菌预防肠道炎症的确切机制尚未完全阐明。本研究旨在评估副干酪乳杆菌亚种。乳脂 FC 使用体内和体外炎症模型的抗炎作用。通过在饮用水中给予 3%葡聚糖硫酸钠诱导 C57BL/6 小鼠结肠炎。在细胞水平评估中,使用由 LPS 刺激的 Caco-2 细胞和 RAW264.7 细胞共培养系统的肠道炎症模型。副干酪乳杆菌亚种。乳脂 FC 的给药显著改善了 DSS 诱导的结肠炎小鼠结肠长度缩短和结肠组织学评分。此外,通过显著抑制 TNF-α(P<0.05)、IFN-γ(P<0.05)、IL-6、iNOS 和 MIP-2 mRNA 表达,将副干酪乳杆菌亚种。乳脂 FC 的治疗使炎症组织中异常的 mRNA 表达接近对照水平得到改善。此外,在肠道炎症模型中,副干酪乳杆菌亚种。乳脂 FC 的治疗导致 Caco-2 细胞中 IL-8 mRNA 表达的显著下调和 RAW264.7 细胞中 NF-κB 核易位的抑制。我们的研究结果表明,副干酪乳杆菌亚种。乳脂 FC 的给药通过抑制炎症细胞浸润改善 DSS 诱导的结肠炎对小鼠的负面影响。