Evidence map›Paper›PMID 37712266›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2023

[Acetylcorynoline relieves 2, 4, 6-trinitrobenesulfonic acid-induced Crohn's disease-like colitis in mice by regulating intestinal epithelial cell apoptosis].

Q Li, J Huang, Y Sun, Y Xu, L Wang, X Zhang, Y Wang, Z Geng, X Song, L Zuo and 2 more

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 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
–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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. [Cimifugin ameliorates Crohn's disease-like colitis in mice by modulating Th-cell immune balanceNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
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

12 authors.

Q LiClinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
J HuangClinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
Y SunDepartment of Laboratory Medicine, Bengbu Medical College, Bengbu 233030, China.
Y XuDepartment of Laboratory Medicine, Bengbu Medical College, Bengbu 233030, China.
L WangDepartment of Gastrointestinal Surgery, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
X ZhangCentral Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
Y WangClinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
Z GengCentral Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
X SongCentral Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
L ZuoDepartment of Gastrointestinal Surgery, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
J LiClinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
J HuClinical Laboratory, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the effect of acetylcorynoline for relieving 2, 4, 6-trinitrobenzenesulfonic acid (TNBS)-induced Crohn's disease (CD)-like colitis in mice and explore the underlying mechanism.

methodsMale C57BL/6 mice were subjected to TNBS treatment to establish models of TNBS-induced CD-like colitis, followed by treatment with saline or 10, 20, or 40 mg/kg acetylcorynoline by gavage. The protective effect of acetylcorynoline against colitis was evaluated by monitoring body weight changes, measurement of DAI and colon length, and histological examination. The colon tissues and cultured colon organoids treated with LPS and acetylcorynoline were examined for expressions of tight junction proteins and apoptosis-related proteins using immunofluorescence assay, Western blotting, and TUNEL staining. The mechanism of acetylcorynoline-induced inhibition of intestinal epithelial cell apoptosis was predicted by network pharmacology and verified by Western blotting.

resultsAcetylcorynoline treatment significantly alleviated weight loss and colon length shortening and reduced DAI score and inflammation score in TNBS mice (

conclusionAcetylcorynoline protects against TNBS-induced CDlike colitis in mice possibly by suppressing the activation of the PI3K/AKT signaling pathway, thereby inhibiting apoptosis of the intestinal epithelial cells.

Indexed as

ColitisCrohn DiseaseAnimalsApoptosisbcl-2-Associated X ProteinBerberine AlkaloidsClaudin-1Epithelial CellsMaleMiceMice, Inbred C57BLPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktacetylcorynolinebcl-2-Associated X ProteinBerberine AlkaloidsClaudin-1Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktacetylcorynolineCrohn's diseaseintestinal epithelial cell apoptosisPI3K/AKT

Identifiers

PMID37712266
PMCPMC10505581

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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.