Evidence map›Paper›PMID 17409121›Full record

ArticleGut2007

Experimental acute pancreatitis in PAP/HIP knock-out mice.

Meritxell Gironella, Emma Folch-Puy, Aude LeGoffic, Stéphane Garcia, Laurence Christa, Andrew Smith, Luis Tebar, Stephen P Hunt, Rosemary Bayne, Andrew J H Smith and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Gut, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 84 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Myeloid-specific dopamine DBritish journal of pharmacology · 2020
    Article
  12. Review
  13. Article
  14. Article
  15. Reg3 Proteins as Gut Hormones?Endocrinology · 2019
    Review
  16. Review
  17. Up-regulation ofBiochemistry and biophysics reports · 2017
    Article
  18. Article
  19. Article
  20. Mechanisms of interleukin-22's beneficial effects in acute pancreatitis.World journal of gastrointestinal pathophysiology · 2016
    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 5 institutions in 3 countries.

Meritxell GironellaINSERM, U.624, Marseille, France.
Emma Folch-Puy
Aude LeGoffic
Stéphane Garcia
Laurence Christa
Andrew Smith
Luis Tebar
Stephen P Hunt
Rosemary Bayne
Andrew J H Smith
Jean-Charles Dagorn
Daniel Closa
Juan L Iovanna
Inserm · FRUniversity of Edinburgh · GBInstitut d'Investigacions Biomèdiques de Barcelona · ESUniversity College London · GBHôpital Necker-Enfants Malades · FR

Funding

Medical Research Council G0000865
6 · The paper itself

Abstract

BACKGROUND AND

aimsPAP/HIP was first reported as an additional pancreatic secretory protein expressed during the acute phase of pancreatitis. It was shown in vitro to be anti-apoptotic and anti-inflammatory. This study aims to look at whether PAP/HIP plays the same role in vivo.

methodsA model of caerulein-induced pancreatitis was used to compare the outcome of pancreatitis in PAP/HIP(-/-) and wild-type mice.

resultsPAP/HIP(-/-) mice showed the normal phenotype at birth and normal postnatal development. Caerulein-induced pancreatic necrosis was, however, less severe in PAP/HIP(-/-) mice than in wild-type mice, as judged by lower amylasemia and lipasemia levels and smaller areas of necrosis. On the contrary, pancreas from PAP/HIP(-/-) mice was more sensitive to apoptosis, in agreement with the anti-apoptotic effect of PAP/HIP in vitro. Surprisingly, pancreatic inflammation was more extensive in PAP/HIP(-/-) mice, as judged from histological parameters, increased myeloperoxidase activity and increased pro-inflammatory cytokine expression. This result, in apparent contradiction with the limited necrosis observed in these mice, is, however, in agreement with the anti-inflammatory function previously reported in vitro for PAP/HIP. This is supported by the observation that activation of the STAT3/SOCS3 pathway was strongly decreased in the pancreas of PAP/HIP(-/-) mice and by the reversion of the apoptotic and inflammatory phenotypes upon administration of recombinant PAP/HIP to PAP/HIP(-/-) mice.

conclusionThe anti-apoptotic and anti-inflammatory functions described in vitro for PAP/HIP have physiological relevance in the pancreas in vivo during caerulein-induced pancreatitis.

Indexed as

Acute DiseaseAnimalsApoptosisAutoantigensCeruletideDisease Models, AnimalLithostathineMiceMice, KnockoutNecrosisPancreasPancreatitisPancreatitis-Associated ProteinsPhenotypeProteinsSTAT3 Transcription FactorAutoantigensCeruletideLithostathinePancreatitis-Associated ProteinsProteinsReg1 protein, mouseReg3b protein, mouseRegIII protein, mouseRegII protein, mouseSocs3 protein, mouseStat3 protein, mouseSTAT3 Transcription FactorSuppressor of Cytokine Signaling 3 ProteinSuppressor of Cytokine Signaling Proteins

Identifiers

PMID17409121
PMCPMC1955488
OpenAlexW2170619545

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.