Evidence map›Paper›PMID 18493729›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2008

Targeting endocannabinoid degradation protects against experimental colitis in mice: involvement of CB1 and CB2 receptors.

Martin A Storr, Catherine M Keenan, Dominik Emmerdinger, Hong Zhang, Birol Yüce, Andrei Sibaev, Federico Massa, Nancy E Buckley, Beat Lutz, Burkhard Göke and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

79 citing papers in PubMed, 166 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. The Impact of the CBMolecules (Basel, Switzerland) · 2024
    Review
  6. Review
  7. Cannabinoids in the Modulation of Oxidative Signaling.International journal of molecular sciences · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Role of the Endocannabinoid System in the Regulation of Intestinal Homeostasis.Cellular and molecular gastroenterology and hepatology · 2022
    Review
  14. Review
  15. Review
  16. Comorbid anxiety-like behavior in a rat model of colitis is mediated by an upregulation of corticolimbic fatty acid amide hydrolase.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
  17. Review
  18. Review
  19. Article
  20. Article

19 more citing papers are in PubMed but not listed here.

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

13 authors at 5 institutions in 4 countries.

Martin A StorrDivision of Gastroenterology, Department of Medicine, University of Calgary, Calgary, Alberta, Canada. mstorr@ucalgary.ca
Catherine M Keenan
Dominik Emmerdinger
Hong Zhang
Birol Yüce
Andrei Sibaev
Federico Massa
Nancy E Buckley
Beat Lutz
Burkhard Göke
Stephan Brand
Kamala D Patel
Keith A Sharkey
Ludwig-Maximilians-Universität München · DEUniversity of Calgary · CACalifornia State Polytechnic University · USJohannes Gutenberg University Mainz · DENeurocentre Magendie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endocannabinoid (EC) system mediates protection against intestinal inflammation. In this study, we investigated the effects of blocking EC degradation or cellular reuptake in experimental colitis in mice. Mice were treated with trinitrobenzene-sulfonic acid in presence and absence of the fatty acid amide hydrolase (FAAH) blocker URB597, the EC membrane transport inhibitor VDM11, and combinations of both. Inflammation was significantly reduced in the presence of URB597, VDM11, or both as evaluated by macroscopic damage score, myeloperoxidase levels, and colon length. These effects were abolished in CB(1)- and CB(2)-receptor-gene-deficient mice. Quantitative reverse transcription polymerase chain reaction after induction of experimental colitis by different pathways showed that expression of FAAH messenger RNA (mRNA) is significantly reduced in different models of inflammation early in the expression of colitis, and these return to control levels as the disease progresses. Genomic DNA from 202 patients with Crohn's disease (CD) and 206 healthy controls was analyzed for the C385A polymorphism in the FAAH gene to address a possible role in humans. In our groups, the C385A polymorphism was equally distributed in patients with CD and healthy controls. In conclusion, drugs targeting EC degradation offer therapeutic potential in the treatment of inflammatory bowel diseases. Furthermore, reduction of FAAH mRNA expression is involved in the pathophysiological response to colitis.

Indexed as

EndocannabinoidsAmidohydrolasesAnimalsArachidonic AcidsBenzamidesCannabinoid Receptor ModulatorsCarbamatesColitisCrohn DiseaseDisease Models, AnimalFatty Acid Amide HydrolasesHumansMiceMice, Inbred C57BLPolymorphism, GeneticReceptor, Cannabinoid, CB1AmidohydrolasesArachidonic AcidsBenzamidesCannabinoid Receptor ModulatorsCarbamatescyclohexyl carbamic acid 3'-carbamoylbiphenyl-3-yl esterEndocannabinoidsFatty Acid Amide HydrolasesN-(2-methyl-3-hydroxyphenyl)-5,8,11,14-eicosatetraenamideReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2RNA, MessengerTrinitrobenzenesulfonic Acid

Identifiers

PMID18493729
OpenAlexW2113468310

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.