Evidence map›Paper›PMID 36759174›Full record

ArticleLife science alliance2023

Tannins amount determines whether tannase-containing bacteria are probiotic or pathogenic in IBD.

Qiuyue He, Kenan Guo, Lulu Wang, Fei Xie, Qingyuan Zhao, Xianhong Jiang, Zhongming He, Peng Wang, Shiqiang Li, Yan Huang and 9 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 2 countries.

Qiuyue HeDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Kenan GuoDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Lulu WangDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Fei XieDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Qingyuan ZhaoDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Xianhong JiangDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Zhongming HeDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Peng WangDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Shiqiang LiDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Yan HuangDepartment of Pharmaceutics, College of Pharmacy, Army Medical University, Chongqing, China.
Cong ZhangDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Rongjuan HuangDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Yang LiuDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Fengchao WangState Key Laboratory of Trauma, Burns and Combined Injury, Institute of Combined Injury, Chongqing Engineering Research Center for Nanomedicine, College of Preventive Medicine, Army Medical University, Chongqing, China.
Xiaoyang ZhouDepartment of Biological Safety, Army Medical University, Chongqing, China.
Rong NiuDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China.
Tao ZuoGuangdong Institute of Gastroenterology, The Sixth Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Yong WangDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China yongw7528@hotmail.com lcg20050502@aliyun.com.ORCID https://orcid.org/0000-0001-8659-3684
Chuangen LiDepartment of Laboratory Animal Science, Army Medical University, Chongqing, China yongw7528@hotmail.com lcg20050502@aliyun.com.ORCID https://orcid.org/0000-0002-1977-4298
Army Medical University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of dietary tannin in inflammatory bowel disease (IBD) is still not clear. Therefore, we aim to study the effect of TA in the progression of IBD. Dextran sulphate sodium (DSS)-induced model was used to mimic IBD. Metagenomics and metabolomics were performed to study the alteration of intestinal microbiota and metabolites. NCM460 and THP-1 cells were used for in vitro study. The amount of TA was associated with the outcomes of DSS-induced IBD as evidenced by in vivo and in vitro studies. Metabolomic and metagenomic analyses revealed that TA-induced enrichment of microbial metabolite gallic acid (GA) was responsible for the action of TA. Mechanistically, protective dose of GA promoted colonic mucus secretion to suppress bacterial infection and that it ameliorated DSS-induced epithelial damage by inhibiting p53 signaling, whereas toxic dose of GA directly caused epithelial damage by promoting cell cycle arrest. Therapeutic experiment showed protective dose of GA-promoted recovery of DSS-induced colonic inflammation. The role of tannase-containing bacteria can be transformed under different conditions in IBD progression.

Indexed as

ColitisInflammatory Bowel DiseasesProbioticsBacteriaCarboxylic Ester HydrolasesHumansTanninsCarboxylic Ester HydrolasestannaseTannins

Identifiers

PMID36759174
PMCPMC9911794
OpenAlexW4319719251

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.