Evidence map›Paper›PMID 32403397›Full record

ArticleBiomolecules2020

Transient Expression of Reck Under Hepatic Ischemia/Reperfusion Conditions Is Associated with Mapk Signaling Pathways.

Andrea Ferrigno, Laura G Di Pasqua, Giuseppina Palladini, Clarissa Berardo, Roberta Verta, Plinio Richelmi, Stefano Perlini, Debora Collotta, Massimo Collino, Mariapia Vairetti

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Changes in Glutathione Content in Liver Diseases: An Update.Antioxidants (Basel, Switzerland) · 2021
    Review
  8. 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 2 institutions in 1 country.

Andrea FerrignoDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
Laura G Di PasquaDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
Giuseppina PalladiniDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
Clarissa BerardoDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
Roberta VertaDepartment of Drug Science and Technology, University of Turin, 10125 Turin, Italy.
Plinio RichelmiDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
Stefano PerliniDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
Debora CollottaDepartment of Drug Science and Technology, University of Turin, 10125 Turin, Italy.
Massimo CollinoDepartment of Drug Science and Technology, University of Turin, 10125 Turin, Italy.
Mariapia VairettiDepartment of Internal Medicine and Therapeutics, University of Pavia, 27100 Pavia, Italy.
University of Pavia · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we demonstrated the involvement of matrix metalloproteinases (MMPs) in hepatic ischemia/reperfusion (I/R) injury. Our aim is to evaluate the impact of reperfusion on I/R-related changes in RECK, an MMP modulator, and mitogen-activated protein kinase (MAPKs) pathways (ERK, p38, and JNK). Male Wistar rats were either subjected to 60 min partial-hepatic ischemia or sham-operated. After a 60 min or 120 min reperfusion, liver samples were collected for analysis of MMP-2 and MMP-9 by zymography and RECK, TIMP-1, and TIMP-2 content, MAPKs activation (ERK1/2, JNK1/2, and p38), as well as iNOS and eNOS by Western blot. Serum enzymes AST, ALT, and alkaline-phosphatase were quantified. A transitory decrease in hepatic RECK and TIMPs was associated with a transitory increase in both MMP-2 and MMP-9 activity and a robust activation of ERK1/2, JNK1/2, and p38 were detected at 60 min reperfusion. Hepatic expression of iNOS was maximally upregulated at 120 min reperfusion. An increase in eNOS was detected at 120 min reperfusion. I/R evoked significant hepatic injury in a time-dependent manner. These findings provide new insights into the underlying molecular mechanisms of reperfusion in inducing hepatic injury: a transitory decrease in RECK and TIMPs and increases in both MAPK and MMP activity suggest their role as triggering factors of the organ dysfunction.

Indexed as

MAP Kinase Signaling SystemAnimalsGPI-Linked ProteinsLiverMaleMatrix MetalloproteinasesNitric Oxide Synthase Type IINitric Oxide Synthase Type IIIRats, WistarReperfusion InjuryTissue Inhibitor of MetalloproteinasesTumor Suppressor ProteinsGPI-Linked ProteinsMatrix MetalloproteinasesNitric Oxide Synthase Type IINitric Oxide Synthase Type IIIReck protein, ratTissue Inhibitor of MetalloproteinasesTumor Suppressor ProteinseNOSiNOS.ischemia/reperfusionMAPKsmatrix metalloproteinaseRECK

Identifiers

PMID32403397
PMCPMC7277810
OpenAlexW3022888936

What OpenQuestion holds

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LicenceCC BY
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.