Evidence map›Paper›PMID 19033539›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2009

Protective role of angiotensin II type 2 receptor signaling in a mouse model of pancreatic fibrosis.

Barbara Ulmasov, Zekuan Xu, Laura H Tetri, Tadashi Inagami, Brent A Neuschwander-Tetri

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Article
  2. Angiotensin receptor signaling and prostate tumor growth in mice.Journal of experimental therapeutics & oncology · 2017
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. The Angiotensin II Type 2 Receptor in Brain Functions: An Update.International journal of hypertension · 2012
    Article
  12. Review
  13. Article
  14. LOX-1 and angiotensin receptors, and their interplay.Cardiovascular drugs and therapy · 2011
    Review
  15. Article
  16. New insights into angiotensin receptor actions: from blood pressure to aging.Current opinion in nephrology and hypertension · 2011
    Review
  17. Article
  18. 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

5 authors.

Barbara UlmasovDepartment of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO 63110, USA.
Zekuan Xu
Laura H Tetri
Tadashi Inagami
Brent A Neuschwander-Tetri

Funding

Molecular mechanisms of pancreatic fibrogenesisR01DK061992 · NIDDK · SAINT LOUIS UNIVERSITY · PI NEUSCHWANDER-TETRI, BRENT A · 2004 to 2007
$1.0M
NIDDK NIH HHS R01-DK-61992
6 · The paper itself

Abstract

The renin-angiotensin system contributes to pathological processes in a variety of organs. In the pancreas, blocking the angiotensin II (AII) type 1 receptor (AT1) attenuates pancreatic fibrogenesis in animal models of pancreatitis. Because the role of the AII type 2 receptor (AT2) in modulating pancreatic injury is unknown we investigated the role of AT2 in pancreatic injury and fibrosis. Pancreatic fibrosis was induced by repetitive cerulein administration in C57BL/6 wild-type (WT) or AT2-deficient (AT2-/-) mice and assessed by morphology and gene expression at 10 days. There was no difference between WT and AT2-/- mice in the degree of acute pancreatic injury as assessed by amylase release at 9 and 12 h and by histological examination of the pancreas at 12 h. In contrast, parenchymal atrophy and fibrosis were more pronounced in AT2-/- mice compared with WT mice at 10 days. Fibrosis was accompanied by activation of pancreatic stellate cells (PSC) evaluated by Western blot analysis for alpha-smooth muscle actin and by immunocytochemistry; PSC activation was further increased in AT2-/- mice compared with WT mice. The level of pancreatic transforming growth factor-beta1 mRNA and protein after repetitive cerulein treatment was higher in AT2-/- mice than in WT mice. Our results demonstrate that, in contrast to AT1 receptor signaling, AT2 receptor signaling modulates protective antifibrogenic effects in a mouse model of cerulein-induced pancreatic fibrogenesis. We propose that the effects of AII on injury-induced pancreatic fibrosis may be determined by the balance between AT1 and AT2 receptor signaling.

Indexed as

Signal TransductionActinsAcute DiseaseAmylasesAngiotensinsAnimalsCeruletideCollagenDisease Models, AnimalFemaleFibrosisMaleMiceMice, Inbred C57BLMice, KnockoutPancreasActinsAmylasesAngiotensinsCeruletideCollagenReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2RNA, MessengerTransforming Growth Factor beta1

Identifiers

PMID19033539
PMCPMC2643909

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.