Evidence map›Paper›PMID 39707318›Full record

ArticleJournal of translational medicine2024

Conjugated bile acids alleviate acute pancreatitis through inhibition of TGR5 and NLRP3 mediated inflammation.

Zi-Yi Zhang, Xiu-Liu Guo, Jing-Tian-Yi Liu, Yi-Jie Gu, Xing-Wei Ji, Shu Zhu, Jin-Yan Xie, Feng Guo

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Expanding bile acid diversityNatural product reports · 2026
    Review
  2. Article
  3. Article
  4. Review
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  7. Article
  8. Article
  9. Review
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  12. [Research progress on the microbiota-immune-metabolism axis in childhood obesity-related asthma].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    Review
  13. 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

8 authors.

Zi-Yi ZhangKey Laboratory of Animal Virology of Ministry of Agriculture, Center for Veterinary Sciences, Zhejiang University, Hangzhou, People's Republic of China.
Xiu-Liu GuoDepartment of Critical Care Medicine, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China.
Jing-Tian-Yi LiuKey Laboratory of Animal Virology of Ministry of Agriculture, Center for Veterinary Sciences, Zhejiang University, Hangzhou, People's Republic of China.
Yi-Jie GuState Key Laboratory of Pathogen and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, People's Republic of China.
Xing-Wei JiKey Laboratory of Animal Virology of Ministry of Agriculture, Center for Veterinary Sciences, Zhejiang University, Hangzhou, People's Republic of China.
Shu ZhuKey Laboratory of Animal Virology of Ministry of Agriculture, Center for Veterinary Sciences, Zhejiang University, Hangzhou, People's Republic of China.
Jin-Yan XieDepartment of Critical Care Medicine, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China. xiejinyan1110@zju.edu.cn.
Feng GuoDepartment of Critical Care Medicine, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, People's Republic of China. 3408003@zju.edu.cn.

Funding

Co-construction science and technology program of Zhejiang Traditional Chinese Medicine Administration GZY-ZJ-KJ-24032Natural Science Foundation of Zhejiang Province LZ24H030002Science and Technology Program of Zhejiang Province 2024C03201
6 · The paper itself

Abstract

introductionSevere acute pancreatitis (SAP) is a crucial gastrointestinal disease characterized by systemic inflammatory responses and persistent multiple organ failure. The role of bile acids (BAs) in diverse inflammatory diseases is increasingly recognized as crucial, but the underlying role of BA conjugation remains elusive.

objectivesOur study aim to investigate the potential role of conjugated bile acids in SAP and reveal the molecular mechanisms underlying its regulatory effects. We hypothesized that taurochenodeoxycholic acid (TCDCA) and glycochenodeoxycholic acid (GCDCA) could protect SAP through inhibiting the activation of NLRP3 inflammasomes via the TGR5 pathway in macrophages.

methodsTo test our hypothesis, we used BA-CoA: amino acid N-acyltransferase knockout (Baat

resultsBA-CoA: Amino acid N-acyltransferase knockout (Baat

conclusionConjugated bile acids significantly inhibit NLRP3 inflammasome activation by activating TGR5 pathway, thereby alleviating pancreatic immunopathology. The results provide new insights into the variability of clinical outcomes and paves the way for developing more effective therapeutic interventions for AP.

Indexed as

Bile Acids and SaltsInflammationMice, KnockoutNLR Family, Pyrin Domain-Containing 3 ProteinPancreatitisReceptors, G-Protein-CoupledAcute DiseaseAnimalsDisease Models, AnimalHumansInflammasomesMacrophagesMaleMiceMice, Inbred C57BLBile Acids and SaltsGpbar1 protein, mouseInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseReceptors, G-Protein-CoupledAcute pancreatitisBile acidNLRP3 inflammasomeTCDCATGR5

Identifiers

PMID39707318
PMCPMC11662532

What OpenQuestion holds

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Registered trials

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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.