Evidence map›Paper›PMID 29867564›Full record

ArticleFrontiers in physiology2018

Notch1 Mediates Preconditioning Protection Induced by GPER in Normotensive and Hypertensive Female Rat Hearts.

Carmine Rocca, Saveria Femminò, Giorgio Aquila, Maria C Granieri, Ernestina M De Francesco, Teresa Pasqua, Damiano C Rigiracciolo, Francesca Fortini, Maria C Cerra, Marcello Maggiolini and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 45 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

14 authors at 3 institutions in 1 country.

Carmine RoccaLaboratory of Molecular and Cellular Cardiac Physiology, Department of Biology, Ecology and E.S., University of Calabria, Rende, Italy.
Saveria FemminòDepartment of Biological and Clinical Sciences, University of Turin, Turin, Italy.
Giorgio AquilaDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Maria C GranieriLaboratory of Molecular and Cellular Cardiac Physiology, Department of Biology, Ecology and E.S., University of Calabria, Rende, Italy.
Ernestina M De FrancescoDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Teresa PasquaLaboratory of Molecular and Cellular Cardiac Physiology, Department of Biology, Ecology and E.S., University of Calabria, Rende, Italy.
Damiano C RigiraccioloDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Francesca FortiniDepartment of Medical Sciences, University of Ferrara, Ferrara, Italy.
Maria C CerraLaboratory of Molecular and Cellular Cardiac Physiology, Department of Biology, Ecology and E.S., University of Calabria, Rende, Italy.
Marcello MaggioliniDepartment of Pharmacy, Health and Nutritional Sciences, University of Calabria, Rende, Italy.
Pasquale PagliaroDepartment of Biological and Clinical Sciences, University of Turin, Turin, Italy.
Paola RizzoMaria Cecilia Hospital, GVM Care & Research, E.S. Health Science Foundation, Cotignola, Italy.
Tommaso AngeloneLaboratory of Molecular and Cellular Cardiac Physiology, Department of Biology, Ecology and E.S., University of Calabria, Rende, Italy.
Claudia PennaDepartment of Biological and Clinical Sciences, University of Turin, Turin, Italy.
University of Calabria · ITUniversity of Ferrara · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled estrogen receptor (GPER) is an estrogen receptor expressed in the cardiovascular system. G1, a selective GPER ligand, exerts cardiovascular effects through activation of the PI3K-Akt pathway and Notch signaling in normotensive animals. Here, we investigated whether the G1/GPER interaction is involved in the limitation of infarct size, and improvement of post-ischemic contractile function in female spontaneous hypertensive rat (SHR) hearts. In this model, we also studied Notch signaling and key components of survival pathway, namely PI3K-Akt, nitric oxide synthase (NOS) and mitochondrial K

Indexed as

cardioprotectionH9c2isolated rat heartsNOSPI3K/Aktpreconditioningreperfusion injury salvage kinases

Identifiers

PMID29867564
PMCPMC5962667
OpenAlexW2800845865

What OpenQuestion holds

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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.