Impact of short-chain fatty acid supplementation on gut inflammation and microbiota composition in a murine colitis model

某种肠道细菌 肠道菌群 丁酸盐 阿克曼西亚 生物 结肠炎 微生物学 炎症 盲肠 流式细胞术 TLR5型 乳酸菌 免疫学 食品科学 发酵 生态学 TLR2型 TLR4型
作者
Jae Gon Lee,Ji‐Young Lee,A-reum Lee,Su Vin Jo,Chan Hyuk Park,Dong Soo Han,Chang Soo Eun
出处
期刊:Journal of Nutritional Biochemistry [Elsevier BV]
卷期号:101: 108926-108926 被引量:79
标识
DOI:10.1016/j.jnutbio.2021.108926
摘要

Short-chain fatty acids (SCFAs) play a pivotal role in maintaining intestinal homeostasis. We aimed to investigate the effects of SCFA supplementation on gut inflammation and microbiota composition in a murine colitis model. Mice were fed with sodium butyrate or a mixture of SCFAs in the drinking water for 2 weeks, followed by 2% dextran sulfate sodium (DSS) for 7 d. After euthanasia, mouse colons were extracted to examine histological findings. Flow cytometry of the mouse colon tissues was performed to assess T cell differentiation. Changes in gut microbiota were assessed by high-throughput sequencing of the mouse feces. There were no significant differences in weight change, colonic length, or histologic inflammation score between the DSS, butyrate, and SCFA mix groups. However, flow cytometry revealed that both the expression of CD4+Foxp3+ regulatory T cells and of IL-17-producing T cells were increased in the butyrate and SCFA mix groups. Microbial compositions of the butyrate and SCFA mix groups were significantly different from those of the control and DSS groups in principal coordinate analysis. Relative abundances of the phyla Verrucomicrobia and Proteobacteria, species Akkermansia muciniphila and Escherichia fergusonii were increased in the butyrate and SCFA mix groups. Genera Roseburia and Lactobacillus showed a negative correlation with the degree of colitis, whereas genera Escherichia and Mucispirillum showed a positive correlation. SCFA supplementation did not result in a significant reduction in colon inflammation, but it promoted both regulatory T cell and IL-17-producing T cell expression, and increased both protective and aggressive gut microbiota.
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