Evidence map›Paper›PMID 24530133›Full record

ArticleJournal of Crohn's & colitis2014

Experimental colitis in mice is attenuated by changes in the levels of endocannabinoid metabolites induced by selective inhibition of fatty acid amide hydrolase (FAAH).

M Sałaga, A Mokrowiecka, P K Zakrzewski, A Cygankiewicz, E Leishman, M Sobczak, H Zatorski, E Małecka-Panas, R Kordek, M Storr and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of Crohn's & colitis, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
12.7field-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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. The Impact of the CBMolecules (Basel, Switzerland) · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Role of the Endocannabinoid System in the Regulation of Intestinal Homeostasis.Cellular and molecular gastroenterology and hepatology · 2022
    Review
  13. 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. Article
  18. Article
  19. Review
  20. Cannabinoids in Medicine: Cancer, Immunity, and Microbial Diseases.International journal of molecular sciences · 2020
    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

13 authors at 4 institutions in 3 countries.

M SałagaDepartment of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
A MokrowieckaDepartment of Digestive Tract Diseases, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
P K ZakrzewskiDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
A CygankiewiczDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
E LeishmanDepartment of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, IN, USA.
M SobczakDepartment of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
H ZatorskiDepartment of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
E Małecka-PanasDepartment of Digestive Tract Diseases, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
R KordekDepartment of Pathology, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
M StorrDepartment of Medicine, Division of Gastroenterology, Ludwig Maximilians University of Munich, Munich, Germany.
W M KrajewskaDepartment of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
H B BradshawDepartment of Psychological and Brain Sciences, Gill Center for Biomolecular Science, Indiana University, Bloomington, IN, USA.
J FichnaDepartment of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland. Electronic address: jakub.fichna@umed.lodz.pl.
Medical University of Lodz · PLUniversity of Łódź · PLIndiana University Bloomington · USLudwig-Maximilians-Universität München · DE

Funding

Microglial activation by N-arachidonoyl glycineR21DA032150 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI BRADSHAW, HEATHER BRYTE · 2011 to 2012
$424k
NIDA NIH HHS R21 DA032150
6 · The paper itself

Abstract

BACKGROUND AND

aimsPharmacological treatment and/or maintenance of remission in inflammatory bowel diseases (IBD) is currently one of the biggest challenge in the field of gastroenterology. Available therapies are mostly limited to overcoming the symptoms, but not the cause of the disease. Recently, the endocannabinoid system has been proposed as a novel target in the treatment of IBD. Here we aimed to assess the anti-inflammatory action of the novel fatty acid amide hydrolase (FAAH) inhibitor PF-3845 and its effect on the endocannabinoid and related lipid metabolism during the course of experimental colitis.

methodsWe used two models of experimental colitis in mice (TNBS- and DSS-induced) and additionally, we employed LC/MS/MS spectrometry to determine the changes in biolipid levels in the mouse colon during inflammation.

resultsWe showed that the FAAH inhibitor PF-3845 reduced experimental TNBS-induced colitis in mice and its anti-inflammatory action is associated with altering the levels of selected biolipids (arachidonic and oleic acid derivatives, prostaglandins and biolipids containing glycine in the mouse colon).

conclusionsWe show that FAAH is a promising pharmacological target and the FAAH-dependent biolipids play a major role in colitis. Our results highlight and promote therapeutic strategy based on targeting FAAH-dependent metabolic pathways in order to alleviate intestinal inflammation.

Indexed as

AmidohydrolasesAnimalsCannabinoidsColitis, UlcerativeDisease Models, AnimalDose-Response Relationship, DrugFatty Acid Amide HydrolasesIndolesInjections, IntraperitonealMaleMiceMice, Inbred C57BLPiperidinesPyrazolesPyridinesReceptor, Cannabinoid, CB1AM 251AmidohydrolasesCannabinoidsFatty Acid Amide HydrolasesIndolesiodopravadolinePF 3845PiperidinesPyrazolesPyridinesReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Experimental colitisFatty acid amide hydrolase;Inflammatory bowel diseases;Intestinal inflammation;PF-3845;

Identifiers

PMID24530133
PMCPMC4136976
OpenAlexW2134888297

What OpenQuestion holds

Textmetadata
LicenceTDM
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.