结肠炎
炎症性肠病
下调和上调
失调
溃疡性结肠炎
促炎细胞因子
超氧化物歧化酶
双歧杆菌
化学
抗氧化剂
肿瘤坏死因子α
肠道菌群
药理学
微生物学
免疫学
乳酸菌
内科学
炎症
医学
生物
生物化学
疾病
基因
发酵
作者
Jin Xu,Chuankang Tang,Ahmad Ud Din,Yu Lu,Xiaoyu Ma,Tao Zhang,Jiaqi Wu,Du Zuoqin,Pei Luo,Jianbo Wu
标识
DOI:10.1016/j.biopha.2023.114562
摘要
Ulcerative colitis (UC) is one common chronic inflammatory bowel disease that causes severe side effects, and expensive treatment limits effective and sustained treatment of UC. Fructooligosaccharide was isolated from Polygonatum Cyrtonema Hua (PFOS) and exhibits anti-inflammatory effects. Therefore, we are curious whether PFOS could be used for the treatment of UC. PFOS was introduced via intragastric gavage to C57BL/6 J mice exposed to acute colitis induced by DSS. The results showed that doses of PFOS at 2 and 5 mg/kg/day alleviated the DSS-induced histopathological damage and improved intestinal barrier function. qPCR analysis revealed that PFOS exerted a significant downregulation of pro-inflammatory cytokines (TNF-α, IL-1β, and IL-6) and upregulation of antioxidant genes, including superoxide dismutase1 (SOD1), glutathion peroxidase2 (GPX2), and nuclear factor erythroid 2 related factor2 (Nrf2). Furthermore, PFOS suppressed the DSS-induced disruption of the mucosal barrier by downregulating MMP13. Moreover, using 16 S rRNA gene-based microbiota analysis, PFOS could selectively enhance the growth of probiotics, including Bifidobacterium, Alloprevofella, and Alistipes. Our findings indicated that PFOS attenuated DSS-induced colitis in mice, suggesting that PFOS might be used as an efficacious supplement for reducing inflammatory bowel disease.
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