| Literature DB >> 36246281 |
Chuanli Yang1,2, Xinshu Bai3, Tianjiao Hu3, Xin Xue3, Xiaohu Su3, Xuan Zhang3, Teng Wu3, Mingxia Zhang4, Xiaobing Shen1,2, Xiushan Dong3.
Abstract
Functional constipation is a common functional gastrointestinal disease. In our previous study, we found that the gut microbiota structure was disordered and the level of phenylalanine (Phe) in serum was decreased in constipated women. We conducted the present study to elucidate the role of Phe in remodeling the composition of gut microbiota and the relationship between gut microbiota and serum metabolites. Here, we demonstrated that Phe treatment significantly enhanced intestinal motility, suppressed inflammatory responses, and prevented intestinal barrier damage in rats with loperamide (Lop)-induced constipation. By metagenomic sequencing, the disbalanced gut microbial profile was analyzed in constipated rats. Phe treatment reversed changes in the abundance of several gut bacteria at the phylum, genus, and species levels. Further, we observed distinct metabolic patterns in constipated rats through targeted metabolomics and identified constipation-related gut microbial species linked to changes in circulating neurotransmitter metabolites. The abundances of species s_Lactobacillus murinus, s_Enterococcus italicus, s_Lactobacillus animalis, s_Lactobacillus apodemi, s_Enterococcus faecalis, and s_Lactobacillus backii were positively correlated with L-asparagine, L-Glutamic acid, Putrescine, and Spermidine levels. The abundances of s_Lactobacillus johnsonii and s_Butyricimonas virosa were negatively correlated with L-asparagine, L-Glutamic acid, Putrescine, and Spermidine levels. Taken together, our findings suggest that Phe can ameliorate the development of Lop-induced constipation in rats by remodeling the gut microbial community structure and changing metabolite levels.Entities:
Keywords: constipation; gut microbiota; metabolomics; metagenomics; neurotransmitter; phenylalanine
Year: 2022 PMID: 36246281 PMCID: PMC9561758 DOI: 10.3389/fmicb.2022.1018008
Source DB: PubMed Journal: Front Microbiol ISSN: 1664-302X Impact factor: 6.064