Evidence map›Paper›PMID 23681475›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2013

Paradoxical regulation of ChAT and nNOS expression in animal models of Crohn's colitis and ulcerative colitis.

John H Winston, Qingjie Li, Sushil K Sarna

Abstract readComparative Study
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Enteric Nervous System Damage by Food Contaminants: A Pathway to Neurodegeneration?Comprehensive reviews in food science and food safety · 2026
    Pooled it
  2. Article
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  6. Review
  7. Review
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  15. Review
  16. Altered Caecal Neuroimmune Interactions in the Neuroligin-3Frontiers in cellular neuroscience · 2020
    Article
  17. Article
  18. Article
  19. Nitrergic Enteric Neurons in Health and Disease-Focus on Animal Models.International journal of molecular sciences · 2019
    Review
  20. 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

3 authors at 1 institution in 1 country.

John H WinstonDivision of Gastroenterology, Dept. of Internal Medicine, The Univ. of Texas Medical Branch at Galveston, 8.104 Medical Research Bldg., Galveston, TX 77555-1064. jhwinsto@utmb.edu.
Qingjie Li
Sushil K Sarna
The University of Texas Medical Branch at Galveston · US

Funding

CONTROL OF COLONIC MOTILITY IN HEALTH AND DISEASER01DK032346 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI SARNA, SUSHIL K · 1986 to 2012
$4.0M
NIDDK NIH HHS DK-32346NIDDK NIH HHS R01 DK032346
6 · The paper itself

Abstract

Morphological and functional changes in the enteric nervous system (ENS) have been reported in inflammatory bowel disease. We examined the effects of inflammation on the expression of choline acetyltransferase (ChAT) and nNOS in the muscularis externae of two models of colonic inflammation, trinitrobenzene sulfonic acid (TNBS)-induced colitis, which models Crohn's disease-like inflammation, and DSS-induced colitis, which models ulcerative Colitis-like inflammation. In TNBS colitis, we observed significant decline in ChAT, nNOS, and protein gene product (PGP) 9.5 protein and mRNA levels. In DSS colitis, ChAT and PGP9.5 were significantly upregulated while nNOS levels did not change. The nNOS dimer-to-monomer ratio decreased significantly in DSS- but not in TNBS-induced colitis. No differences were observed in the percentage of either ChAT (31 vs. 33%)- or nNOS (37 vs. 41%)-immunopositive neurons per ganglia or the mean number of neurons per ganglia (55 ± 5 vs. 59 ± 5, P > 0.05). Incubation of the distal colon muscularis externae in vitro with different types of inflammatory mediators showed that cytokines decreased ChAT and nNOS expression, whereas H₂O₂, a component of oxidative stress, increased their expression. NF-κB inhibitor MG-132 did not prevent the IL-1β-induced decline in either ChAT or nNOS expression. These findings showed that TNBS- and DSS-induced inflammation differentially regulates the expression of two critical proteins expressed in the colonic myenteric neurons. These differences are likely due to the exposure of the myenteric plexus neurons to different combinations of Th1-type inflammatory mediators and H₂O₂ in each model.

Indexed as

AcetylcholineAnimalsBlotting, WesternCholine O-AcetyltransferaseColitis, UlcerativeColonCrohn DiseaseCytokinesDextran SulfateDisease Models, AnimalDose-Response Relationship, DrugGene Expression Regulation, EnzymologicHydrogen PeroxideInflammation MediatorsLeupeptinsMaleAcetylcholinebenzyloxycarbonylleucyl-leucyl-leucine aldehydeCholine O-AcetyltransferaseCytokinesDextran SulfateHydrogen PeroxideInflammation MediatorsLeupeptinsNF-kappa BNitric OxideNitric Oxide Synthase Type INos1 protein, ratRNA, MessengerTrinitrobenzenesulfonic AcidUbiquitin ThiolesteraseUCHL1 protein, ratcholine acetyltransferaseenteric neuronsmotilityneuronal nitric oxide synthasesmooth muscle

Identifiers

PMID23681475
PMCPMC3891212
OpenAlexW1973829975

What OpenQuestion holds

Textmetadata
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.