scholarly journals Baitouweng Tang ameliorates DSS-induced ulcerative colitis through the regulation of the gut microbiota and bile acids via pathways involving FXR and TGR5

2021 ◽  
Vol 137 ◽  
pp. 111320
Author(s):  
Yong-li Hua ◽  
Ya-qian Jia ◽  
Xiao-song Zhang ◽  
Zi-wen Yuan ◽  
Peng Ji ◽  
...  
2021 ◽  
Vol 27 (24) ◽  
pp. 3609-3629
Author(s):  
Zhen-Huan Yang ◽  
Fang Liu ◽  
Xiao-Ran Zhu ◽  
Fei-Ya Suo ◽  
Zi-jun Jia ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lena Öhman ◽  
Anders Lasson ◽  
Anna Strömbeck ◽  
Stefan Isaksson ◽  
Marcus Hesselmar ◽  
...  

AbstractPatients with ulcerative colitis (UC) have an altered gut microbiota composition, but the microbial relationship to disease activity needs to be further elucidated. Therefore, temporal dynamics of the fecal microbial community during remission and flare was determined. Fecal samples were collected at 2–6 time-points from UC patients during established disease (cohort EST) and at diagnosis (cohort NEW). Sampling range for cohort EST was 3–10 months and for cohort NEW 36 months. Relapses were monitored for an additional three years for cohort EST. Microbial composition was assessed by Genetic Analysis GA-map Dysbiosis Test, targeting ≥ 300 bacteria. Eighteen patients in cohort EST (8 with maintained remission and 10 experiencing a flare), provided 71 fecal samples. In cohort NEW, 13 patients provided 49 fecal samples. The microbial composition showed no clustering related to disease activity in any cohort. Microbial dissimilarity was higher between than within patients for both cohorts, irrespective of presence of a flare. Microbial stability within patients was constant over time with no major shift in overall composition nor modification in the abundance of any specific species. Microbial composition was not affected by intensified medical treatment or linked to future disease course. Thus in UC, the gut microbiota is highly stable irrespective of disease stage, disease activity or treatment escalation. This suggests that prolonged dietary interventions or repeated fecal transplantations are needed to be able to induce permanent alterations of the gut microbiota.


2021 ◽  
Vol 97 ◽  
pp. 107683
Author(s):  
Yongzhi Hua ◽  
Ruiqi Liu ◽  
Min Lu ◽  
Xueneng Guan ◽  
Suyang Zhuang ◽  
...  

Author(s):  
Sarah Rotondo‐Trivette ◽  
Beibei Wang ◽  
Christopher Gayer ◽  
Riddhi Parsana ◽  
Yihui Luan ◽  
...  

2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Samah O Noor ◽  
Karyn Ridgway ◽  
Louise Scovell ◽  
E Katherine Kemsley ◽  
Elizabeth K Lund ◽  
...  

2015 ◽  
Vol 162 ◽  
pp. 7-13 ◽  
Author(s):  
Mingzhang Guo ◽  
Shuo Ding ◽  
Changhui Zhao ◽  
Xinxi Gu ◽  
Xiaoyun He ◽  
...  

Theranostics ◽  
2021 ◽  
Vol 11 (17) ◽  
pp. 8570-8586
Author(s):  
Lingjun Tong ◽  
Haining Hao ◽  
Zhe Zhang ◽  
Youyou Lv ◽  
Xi Liang ◽  
...  

Author(s):  
Jiake Yu ◽  
Hu Zhang ◽  
Liya Chen ◽  
Yufei Ruan ◽  
Yiping Chen ◽  
...  

Children with nonalcoholic fatty liver disease (NAFLD) display an altered gut microbiota compared with healthy children. However, little is known about the fecal bile acid profiles and their association with gut microbiota dysbiosis in pediatric NAFLD. A total of 68 children were enrolled in this study, including 32 NAFLD patients and 36 healthy children. Fecal samples were collected and analyzed by metagenomic sequencing to determine the changes in the gut microbiota of children with NAFLD, and an ultra-performance liquid chromatography coupled to tandem mass spectrometry (UPLC-MS/MS) system was used to quantify the concentrations of primary and secondary bile acids. The associations between the gut microbiota and concentrations of primary and secondary bile acids in the fecal samples were then analyzed. We found that children with NAFLD exhibited reduced levels of secondary bile acids and alterations in bile acid biotransforming-related bacteria in the feces. Notably, the decrease in Eubacterium and Ruminococcaceae bacteria, which express bile salt hydrolase and 7α-dehydroxylase, was significantly positively correlated with the level of fecal lithocholic acid (LCA). However, the level of fecal LCA was negatively associated with the abundance of the potential pathogen Escherichia coli that was enriched in children with NAFLD. Pediatric NAFLD is characterized by an altered profile of gut microbiota and fecal bile acids. This study demonstrates that the disease-associated gut microbiota is linked with decreased concentrations of secondary bile acids in the feces. The disease-associated gut microbiota likely inhibits the conversion of primary to secondary bile acids.


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