Evidence map›Paper›PMID 17724800›Full record

ArticleWorld journal of gastroenterology2007

Therapeutic proteasome inhibition in experimental acute pancreatitis.

Tamás Letoha, Liliána Z Fehér, László Pecze, Csaba Somlai, Ilona Varga, József Kaszaki, Gábor Tóth, Csaba Vizler, László Tiszlavicz, Tamás Takács

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

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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.

Tamás LetohaDepartment of Medical Chemistry, University of Szeged, Dom ter 8, H-6720, Szeged, Hungary. tletoha@yahoo.com
Liliána Z Fehér
László Pecze
Csaba Somlai
Ilona Varga
József Kaszaki
Gábor Tóth
Csaba Vizler
László Tiszlavicz
Tamás Takács
University of Szeged · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo establish the therapeutic potential of proteasome inhibition, we examined the therapeutic effects of MG132 (Z-Leu-Leu-Leu-aldehyde) in an experimental model of acute pancreatitis.

methodsPancreatitis was induced in rats by two hourly intraperitoneal (ip) injections of cholecystokinin octapeptide (CCK; 2 x 100 microg/kg) and the proteasome inhibitor MG132 (10 mg/kg ip) was administered 30 min after the second CCK injection. Animals were sacrificed 4 h after the first injection of CCK.

resultsAdministering the proteasome inhibitor MG132 (at a dose of 10 mg/kg, ip) 90 min after the onset of pancreatic inflammation induced the expression of cell-protective 72 kDa heat shock protein (HSP72) and decreased DNA-binding of nuclear factor-kappaB (NF-kappaB). Furthermore MG132 treatment resulted in milder inflammatory response and cellular damage, as revealed by improved laboratory and histological parameters of pancreatitis and associated oxidative stress.

conclusionOur findings suggest that proteasome inhibition might be beneficial not only for the prevention, but also for the therapy of acute pancreatitis.

Indexed as

Proteasome InhibitorsAcute DiseaseAnimalsBody WeightCholecystokininCysteine Proteinase InhibitorsCytokinesHSP72 Heat-Shock ProteinsLeupeptinsMaleNF-kappa BOrgan SizeOxidative StressPancreasPancreatitisPeroxidasebenzyloxycarbonylleucyl-leucyl-leucine aldehydeCholecystokininCysteine Proteinase InhibitorsCytokinesHSP72 Heat-Shock ProteinsLeupeptinsNF-kappa BPeroxidaseProteasome Inhibitors

Identifiers

PMID17724800
PMCPMC4611577
OpenAlexW142993847

What OpenQuestion holds

Textmetadata
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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.