Evidence map›Paper›PMID 24395090›Full record

ArticleJournal of molecular neuroscience : MN2014

Inhibition of vasoactive intestinal polypeptide (VIP) induces resistance to dextran sodium sulfate (DSS)-induced colitis in mice.

John P Vu, Mulugeta Million, Muriel Larauche, Leon Luong, Joshua Norris, James A Waschek, Charalabos Pothoulakis, Joseph R Pisegna, Patrizia M Germano

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
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  10. Review
  11. Immunomodulatory Roles of PACAP and VIP: Lessons from Knockout Mice.Journal of molecular neuroscience : MN · 2018
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. The Role of Neuropeptides in Mouse Models of Colitis.Journal of molecular neuroscience : MN · 2016
    Review
  18. Article
  19. 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

9 authors at 2 institutions in 1 country.

John P VuCURE/Digestive Diseases Research Center, Department of Medicine, David Geffen School of Medicine, University of California at Los Angeles and VA Greater Los Angeles Health Care System, Los Angeles, CA, USA.
Mulugeta Million
Muriel Larauche
Leon Luong
Joshua Norris
James A Waschek
Charalabos Pothoulakis
Joseph R Pisegna
Patrizia M Germano
University of California, Los Angeles · USVA Greater Los Angeles Healthcare System · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
Modulation of Colonic Response to Stress by Peripheral CRF2 ReceptorsR01DK078676 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MULUGETA, MILLION · 2008 to 2016
$2.2M
Modulation of Colonic Epithelial Permeability by Sex HormonesK01DK088937 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LARAUCHE, MURIEL · 2011 to 2015
$647k
NCI NIH HHS P30 CA016042NIDDK NIH HHS DK-41301NIDDK NIH HHS K01 DK088937NIDDK NIH HHS P30 DK041301NIDDK NIH HHS R01 DK-078676NIDDK NIH HHS R01 DK078676
6 · The paper itself

Abstract

VIP is highly expressed in the colon and regulates motility, vasodilatation, and sphincter relaxation. However, its role in the development and progress of colitis is still controversial. Our aim was to determine the participation of VIP on dextran sodium sulfate (DSS)-induced colonic mucosal inflammation using VIP(-/-) and WT mice treated with VIP antagonists. Colitis was induced in 32 adult VIP(-/-) and 14 age-matched WT litter-mates by giving 2.5 % DSS in the drinking water. DSS-treated WT mice were injected daily with VIP antagonists, VIPHyb (n = 22), PG 97-269 (n = 9), or vehicle (n = 31). After euthanasia, colons were examined; colonic cytokines mRNA were quantified. VIP(-/-) mice were remarkably resistant to DSS-induced colitis compared to WT. Similarly, DSS-treated WT mice injected with VIPHyb (1 μM) or PG 97-269 (1 nM) had significantly reduced clinical signs of colitis. Furthermore, colonic expression of IL-1ϐ, TNF-α, and IL-6 was significantly lower in VIP(-/-) and VIPHyb or PG 97-269 compared to vehicle-treated WT. Genetic deletion of VIP or pharmacological inhibition of VIP receptors resulted in resistance to colitis. These data demonstrate a pro-inflammatory role for VIP in murine colitis and suggest that VIP antagonists may be an effective clinical treatment for human inflammatory bowel diseases.

Indexed as

AnimalsColitisCytokinesDextran SulfateGene DeletionInterleukinsIntestinal MucosaMaleMiceMice, Inbred C57BLNeurotensinRecombinant Fusion ProteinsRNA, MessengerTumor Necrosis Factor-alphaVasoactive Intestinal PeptideCytokinesDextran SulfateInterleukinsNeurotensinRecombinant Fusion ProteinsRNA, MessengerTumor Necrosis Factor-alphaVasoactive Intestinal Peptide(VIP-neurotensin) hybrid antagonist

Identifiers

PMID24395090
PMCPMC4114158
OpenAlexW1975203713

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.