Huang Xingxi, Hu Jutuan, Zhang Heng, Li Ji, Zhu Xi, Liu Yangyang, Liang Yunxiang, Mei Yuxia
State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, People's Republic of China.
Microbiol Spectr. 2023 Mar 28;11(2):e0437022. doi: 10.1128/spectrum.04370-22.
Effects of Clostridium butyricum and chitooligosaccharides (COS), singly and in synbiotic combination, were evaluated in a C57BL/6 mouse model of dextran sulfate (DSS)-induced acute ulcerative colitis (UC). Treatment with C. butyricum and/or COS ameliorated UC symptoms , and the strongest effects were observed for the combination in terms of reduced mortality rates and disease activity indices, increased body weight and colon length, and improved histological features. The C. butyricum and COS combination achieved the following: (i) regulated levels of inflammation-related cytokines (tumor necrosis factor alpha [TNF-α], interleukin-1β [IL-1β], IL-6, IL-10) and had a stronger anti-inflammatory effect than either component alone, based on inhibition of Toll-like receptor 4 (TLR-4)/NF-κB/MAPK signaling pathway activation; (ii) enhanced intestinal barrier function by restoring levels of tight junction proteins (occludin, claudin-1, ZO-1) and MUC2; (iii) increased abundance and diversity of beneficial bacteria (gut microbiota) and reduced levels of pathogenic bacteria; and (iv) enhanced production of short-chain fatty acids. Our findings indicate that the synbiotic C. butyricum and COS combination has strong potential as a therapeutic adjuvant for UC. Ulcerative colitis (UC), an idiopathic intestinal disease characterized by continuous remission/relapse inflammatory cycles in the colonic mucosal layer, has strong adverse effects on patients' quality of life and considerable costs for health care systems. Probiotics, prebiotics, and synbiotics are regarded as potential therapeutic agents for UC, in terms of safety and efficacy. In this study, we present detailed evaluation of effects in a DSS-induced UC mouse model of a synbiotic composed of Clostridium butyricum and COS (molecular weight [MW], 2,500 Da). We found that synergistic (synbiotic) action of the C. butyricum and COS combination is more effective than either factor alone for prevention and/or therapy of UC by regulating gut microbiota and intestinal barrier function. Our findings indicate that C. butyricum and COS in combination has strong potential for development as anti-UC therapeutic drugs or adjuvant agents in pharmaceutical, food, and livestock industries. Highlights include the following. (i) The C. butyricum and COS combination ameliorated clinical UC symptoms and improved colonic morphology. (ii) The C. butyricum and COS combination displayed strong anti-inflammatory and antioxidant effects. (iii) The C. butyricum and COS combination enhanced expression of tight junction proteins. (iv) The C. butyricum and COS combination inhibited the TRL-4/NF-κB/MAPK signaling pathway. (v) The C. butyricum and COS combination modulated gut microbiota abundance and composition.
在葡聚糖硫酸钠(DSS)诱导的急性溃疡性结肠炎(UC)的C57BL/6小鼠模型中,评估了丁酸梭菌和壳寡糖(COS)单独及合生元组合的效果。用丁酸梭菌和/或COS治疗可改善UC症状,就降低死亡率和疾病活动指数、增加体重和结肠长度以及改善组织学特征而言,组合显示出最强的效果。丁酸梭菌和COS组合实现了以下几点:(i)调节炎症相关细胞因子(肿瘤坏死因子α [TNF-α]、白细胞介素-1β [IL-1β]、IL-6、IL-10)的水平,并且基于对Toll样受体4(TLR-4)/核因子κB(NF-κB)/丝裂原活化蛋白激酶(MAPK)信号通路激活的抑制,具有比单独任何一种成分更强的抗炎作用;(ii)通过恢复紧密连接蛋白(闭合蛋白、Claudin-1、闭锁小带蛋白-1)和MUC2的水平来增强肠道屏障功能;(iii)增加有益细菌(肠道微生物群)的丰度和多样性并降低病原菌水平;以及(iv)增强短链脂肪酸的产生。我们的研究结果表明,丁酸梭菌和COS的合生元组合作为UC的治疗佐剂具有强大潜力。溃疡性结肠炎(UC)是一种特发性肠道疾病,其特征在于结肠黏膜层中持续的缓解/复发炎症周期,对患者的生活质量有严重不利影响,并给医疗保健系统带来相当大的成本。就安全性和有效性而言,益生菌、益生元和合生素被视为UC的潜在治疗剂。在本研究中,我们详细评估了由丁酸梭菌和COS(分子量 [MW],2500 Da)组成的合生元在DSS诱导的UC小鼠模型中的效果。我们发现,丁酸梭菌和COS组合的协同(合生元)作用在通过调节肠道微生物群和肠道屏障功能预防和/或治疗UC方面比单独任何一个因素都更有效。我们的研究结果表明,丁酸梭菌和COS组合在制药、食品和畜牧业中作为抗UC治疗药物或佐剂具有强大的开发潜力。要点如下:(i)丁酸梭菌和COS组合改善了临床UC症状并改善了结肠形态。(ii)丁酸梭菌和COS组合显示出强大的抗炎和抗氧化作用。(iii)丁酸梭菌和COS组合增强了紧密连接蛋白的表达。(iv)丁酸梭菌和COS组合抑制了TRL-4/NF-κB/MAPK信号通路。(v)丁酸梭菌和COS组合调节了肠道微生物群的丰度和组成。