Evidence map›Paper›PMID 32977437›Full record

ArticleInternational journal of molecular sciences2020

Cardioprotective Effect of Novel Matrix Metalloproteinase Inhibitors.

Kamilla Gömöri, Tamara Szabados, Éva Kenyeres, Judit Pipis, Imre Földesi, Andrea Siska, György Dormán, Péter Ferdinandy, Anikó Görbe, Péter Bencsik

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Novel Roles of MT1-MMP and MMP-2: Beyond the Extracellular Milieu.International journal of molecular sciences · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. The Synergistic Effects ofDrug design, development and therapy · 2021
    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.

Kamilla GömöriCardiovascular Research Group, Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0001-9793-3138
Tamara SzabadosCardiovascular Research Group, Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.
Éva KenyeresCardiovascular Research Group, Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.
Judit PipisPharmahungary Group, H-6722 Szeged, Hungary.
Imre FöldesiDepartment of Laboratory Medicine, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0002-3329-8136
Andrea SiskaDepartment of Laboratory Medicine, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.
György DormánTargetex Biosciences, H-2120 Dunakeszi, Hungary.
Péter FerdinandyPharmahungary Group, H-6722 Szeged, Hungary.
Anikó GörbeCardiovascular Research Group, Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.
Péter BencsikCardiovascular Research Group, Department of Pharmacology and Pharmacotherapy, Faculty of Medicine, University of Szeged, H-6720 Szeged, Hungary.ORCID 0000-0003-1936-6232
University of Szeged · HUSemmelweis University · HU

Funding

Hungarian National Research, Development and Innovation Office TÉT_15_IN-1-2016-0068, GINOP-2.3.2-15-2016-00040, NVKP 16-1-2016-0017
6 · The paper itself

Abstract

backgroundWe recently developed novel matrix metalloproteinase-2 (MMP-2) inhibitor small molecules for cardioprotection against ischemia/reperfusion injury and validated their efficacy in ischemia/reperfusion injury in cardiac myocytes. The aim of the present study was to test our lead compounds for cardioprotection in vivo in a rat model of acute myocardial infarction (AMI) in the presence or absence of hypercholesterolemia, one of the major comorbidities affecting cardioprotection.

methodsNormocholesterolemic adult male

resultsMMPI-1154 at 1 µmol/kg, MMPI-1260 at 3 µmol/kg and ischemic preconditioning (IPC) as the positive control reduced infarct size significantly; however, this effect was not seen in hypercholesterolemic animals. MVO in hypercholesterolemic animals decreased by IPC only.

conclusionsThis is the first demonstration that MMPI-1154 and MMPI-1260 showed a dose-dependent infarct size reduction in an in vivo rat AMI model; however, single doses that showed the most efficacy in normocholesterolemic animals were abolished by hypercholesterolemia. The further development of these promising cardioprotective MMPIs should be continued with different dose ranges in the study of hypercholesterolemia and other comorbidities.

Indexed as

Cardiotonic AgentsMatrix Metalloproteinase InhibitorsAnimalsDisease Models, AnimalHypercholesterolemiaMaleMyocardial InfarctionMyocardial Reperfusion InjuryRatsRats, WistarCardiotonic AgentsMatrix Metalloproteinase Inhibitorsacute myocardial infarctioncardioprotectioncardiovascular comorbidityhypercholesterolemiamatrix metalloproteinase inhibitorMMP-2thiazole and imidazole carboxylic acid derivatives

Identifiers

PMID32977437
PMCPMC7582346
OpenAlexW3088593180

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.