Evidence map›Paper›PMID 26495793›Full record

ArticlePancreas

Synthetic Triterpenoid RTA dh404 (CDDO-dhTFEA) Ameliorates Acute Pancreatitis.

Lourdes Robles, Nosratola D Vaziri, Shiri Li, Yuichi Masuda, Chie Takasu, Mizuki Takasu, Kelly Vo, Seyed H Farzaneh, Michael J Stamos, Hirohito Ichii

Abstract read
In one paragraph

Article in Pancreas. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Antioxidant Therapy in Pancreatitis.Antioxidants (Basel, Switzerland) · 2021
    Review
  3. Review
  4. Review
  5. Bardoxolone methyl analog attenuates proteinuria-induced tubular damage by modulating mitochondrial function.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  6. 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

10 authors at 1 institution in 1 country.

Lourdes RoblesFrom the Departments of Surgery and Medicine, University of California, Irvine, Orange, CA.
Nosratola D Vaziri
Shiri Li
Yuichi Masuda
Chie Takasu
Mizuki Takasu
Kelly Vo
Seyed H Farzaneh
Michael J Stamos
Hirohito Ichii
University of California, Irvine · US

Funding

Institute for Clinical and Translational ScienceUL1TR000153 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$12.1M
Institute for Clinical and Translational ScienceKL2TR000147 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$940k
NCATS NIH HHS KL2 TR000147
6 · The paper itself

Abstract

objectivesNuclear factor-erythroid-2-related factor (Nrf2) is a ubiquitous transcriptional factor that regulates expression of cellular antioxidant and detoxifying molecules. This study was undertaken to test the hypothesis that administration of the Nrf2 activator (dh404) may attenuate acute pancreatitis.

methodsRats were treated with dh404 (1 mg/kg) 24 hours before induction of pancreatitis and for 3 days thereafter. Pancreatitis was induced with L-arginine (600 mg/100 g) or cerulein (40 μg/kg). Pancreases were processed for histology and malondialdehyde, whereas serum was analyzed for amylase. Islet extracted human pancreatic tissue from organ donors were used for in vitro studies. The tissues were incubated with dh404 at 0, 250, and 500 nM for 30 minutes, 60 minutes, 12 hours, and 24 hours. Nuclear factor-erythroid-2-related factor nuclear translocation and expression of Nrf2's target genes and inflammatory mediators were determined.

resultsThe dh404-treated rat pancreases demonstrated significantly less infiltration of inflammatory cells, destruction of acinar architecture, perilobar edema, and necrosis. Serum amylase and pancreatic malondialdehyde in the dh404-treated rats were significantly lower. dh404-treated human pancreatic tissue showed a significantly higher expression of antioxidant enzymes, lower expression of inflammatory mediators, and greater viability against oxidative stress.

conclusionAdministration of dh404 attenuates acute pancreatitis by lowering oxidative stress and reducing proinflammatory mediators.

Indexed as

Active Transport, Cell NucleusAcute DiseaseAmylasesAnimalsArginineBlotting, WesternCatalaseCell NucleusCeruletideCytokinesDose-Response Relationship, DrugHumansInflammation MediatorsLipopolysaccharidesMalondialdehydeNF-E2-Related Factor 2AmylasesArginineCatalaseCeruletideCytokinesdh404 compoundInflammation MediatorsLipopolysaccharidesMalondialdehydeNfe2l2 protein, ratNF-E2-Related Factor 2Oleanolic AcidSuperoxide Dismutase

Identifiers

PMID26495793
PMCPMC5847282
OpenAlexW1890005850

What OpenQuestion holds

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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.