Evidence map›Paper›PMID 31369209›Full record

ArticleJournal of cellular and molecular medicine2019

Telmisartan cardioprotects from the ischaemic/hypoxic damage through a miR-1-dependent pathway.

Maria Consiglia Trotta, Bartolo Ferraro, Antonietta Messina, Iacopo Panarese, Eliana Gulotta, Giovanni Francesco Nicoletti, Michele D'Amico, Gorizio Pieretti

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 40% 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, 12 citations in OpenAlex.

  1. Review
  2. Impact of microRNAs on cardiovascular diseases and aging.The Journal of international medical research · 2024
    Review
  3. Perspective and Therapeutic Potential of the Noncoding RNA-Connexin Axis.International journal of molecular sciences · 2024
    Review
  4. Review
  5. Review
  6. Article
  7. 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

8 authors at 2 institutions in 1 country.

Maria Consiglia TrottaDepartment of Experimental Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Bartolo FerraroDepartment of Experimental Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Antonietta MessinaDepartment of Experimental Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Iacopo PanareseDepartment of Mental and Physical Health and Preventive Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Eliana GulottaDepartment of Surgical, Oncological and Stomatological Disciplines, University of Palermo, Palermo, Italy.
Giovanni Francesco NicolettiMultidisciplinary Department of Surgical and Dental Specialties, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Michele D'AmicoDepartment of Experimental Medicine, University of Campania 'Luigi Vanvitelli', Naples, Italy.ORCID 0000-0002-6899-0595
Gorizio PierettiMultidisciplinary Department of Surgical and Dental Specialties, University of Campania 'Luigi Vanvitelli', Naples, Italy.
University of Campania "Luigi Vanvitelli" · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate whether telmisartan protects the heart from the ischaemia/reperfusion damage through a local microRNA-1 modulation. Studies on the myocardial ischaemia/reperfusion injury in vivo and on the cardiomyocyte hypoxia/reoxygenation damage in vitro were done. In vivo, male Sprague-Dawley rats administered for 3 weeks with telmisartan 12 mg/kg/d by gastric gavage underwent ischaemia/reperfusion of the left descending coronary artery. In these rats, infarct size measurement, ELISA, immunohistochemistry (IHC) and reverse transcriptase real-time polymerase chain reaction showed that expressions of connexin 43, potassium voltage-gated channel subfamily Q member 1 and the protein Bcl-2 were significantly increased by telmisartan in the reperfused myocardium, paralleled by microRNA-1 down-regulation. In vitro, the transfection of cardiomyocytes with microRNA-1 reduced the expressions of connexin 43, potassium voltage-gated channel subfamily Q member 1 and Bcl-2 in the cells. Telmisartan (50 µmol/L) 60 minutes before hypoxia/reoxygenation, while not affecting the levels of miR-1 in transfected cells in normoxic condition, almost abolished the increment of miR-1 induced by the hypoxia/reoxygenation to transfected cells. All together, telmisartan cardioprotected against the myocardial damage through the microRNA-1 modulation, and consequent modifications of its downstream target connexin 43, potassium voltage-gated channel subfamily Q member 1 and Bcl-2.

Indexed as

AnimalsCell HypoxiaCell LineCell SurvivalConnexin 43KCNQ1 Potassium ChannelMaleMicroRNAsMyocardial InfarctionMyocardial Reperfusion InjuryMyocytes, CardiacProto-Oncogene Proteins c-bcl-2RatsRats, Sprague-DawleyTelmisartanConnexin 43Gja1 protein, ratKCNQ1 Potassium ChannelKcnq1 protein, ratMicroRNAsMIRN1 microRNA, ratProto-Oncogene Proteins c-bcl-2TelmisartanBcl-2connexin 43hypoxic H9c2 cellsKCNQ1miR-1myocardial ischaemia/reperfusiontelmisartan

Identifiers

PMID31369209
PMCPMC6787508
OpenAlexW2965872403

What Socratic 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 Socratic graph.