Bifico relieves irritable bowel syndrome by regulating gut microbiota dysbiosis and inflammatory cytokines

肠道菌群 双歧杆菌 肠易激综合征 失调 乳酸菌 生物 益生菌 丁酸盐 厚壁菌 免疫学 微生物学 内科学 医学 细菌 生物化学 16S核糖体RNA 发酵 遗传学
作者
Yanlin Zhou,Fan Zhang,Li-Qi Mao,Tongfei Feng,Kaijie Wang,Maosheng Xu,Bin Lv,Xi Wang
出处
期刊:European journal of nutrition [Springer Science+Business Media]
卷期号:62 (1): 139-155 被引量:17
标识
DOI:10.1007/s00394-022-02958-0
摘要

Abstract Purpose Gut microbiota dysbiosis, a core pathophysiology of irritable bowel syndrome (IBS), is closely related to immunological and metabolic functions. Gut microbiota-based therapeutics have been recently explored in several studies. Bifico is a probiotic cocktail widely used in gastrointestinal disorders which relate to the imbalance of gut microbiota. However, the efficacy and potential mechanisms of Bifico treatment in IBS remains incompletely understood. Methods Adopting a wrap restraint stress (WRS) -induced IBS mice model. Protective effect of Bifico in IBS mice was examined through abdominal withdrawal reflex (AWR) scores. 16S rDNA, 1 H nuclear magnetic resonance ( 1 H-NMR) and western blot assays were performed to analyze alterations of gut microbiota, microbiome metabolites and inflammatory cytokines, respectively. Results Bifico could decrease intestinal visceral hypersensitivity. Although gut microbiota diversity did not increase, composition of gut microbiota was changed after treatment of Bifico, which were characterized by an increase of Proteobacteria phylum and Actinobacteria phylum, Muribaculum genus, Bifidobacterium genus and a decrease of Parabacteroides genus, Sutterella genus and Lactobacillus genus. Moreover, Bifico elevated the concentration of short-chain fatty acids (SCFAs) and reduced protein levels of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α). From further Spearman’s correlation analysis, Bifidobacterium genus were positively correlated with SCFAs including propionate, butyrate, valerate and negatively correlated with IL-6 and TNF-α. Conclusion Bifico could alleviate symptoms of IBS mice through regulation of the gut microbiota, elevating production of SCFAs and reducing the colonic inflammatory response.

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