Evidence map›Paper›PMID 33297453›Full record

ArticleCells2020

Effect of Beta 3 Adrenoreceptor Modulation on Patency of the Ductus Arteriosus.

Alessandro Pini, Camilla Fazi, Patrizia Nardini, Maura Calvani, Sergio Fabbri, Alessandro Guerrini, Giulia Forni, Giancarlo La Marca, Arianna Carolina Rosa, Luca Filippi

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

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  11. GLP1 Exerts Paracrine Activity in the Intestinal Lumen of Human Colon.International journal of molecular sciences · 2022
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  12. Review
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 5 institutions in 1 country.

Alessandro PiniDepartment of Experimental and Clinical Medicine, University of Florence, 50139 Florence, Italy.ORCID 0000-0001-9828-2082
Camilla FaziDepartment of Health Sciences, University of Florence, 50139 Florence, Italy.
Patrizia NardiniDepartment of Experimental and Clinical Medicine, University of Florence, 50139 Florence, Italy.ORCID 0000-0003-2374-5147
Maura CalvaniDepartment of Paediatric Haematology-Oncology, A. Meyer University Children's Hospital, 50139 Florence, Italy.ORCID 0000-0003-0750-4706
Sergio FabbriDepartment of Neuroscience, Psychology, Drug Research and Child Health, Section of Pharmacology and Toxicology, University of Florence, 50139 Florence, Italy.
Alessandro GuerriniDepartment of Veterinary Medical Sciences, University of Bologna, 40064 Ozzano dell'Emilia, Italy.ORCID 0000-0002-8224-4919
Giulia ForniDepartment of Neuroscience, Psychology, Drug Research and Child Health, Section of Pediatric Neurosciences, "A. Meyer" University Children's Hospital, 50139 Florence, Italy.
Giancarlo La MarcaDepartment of Neuroscience, Psychology, Drug Research and Child Health, Section of Pediatric Neurosciences, "A. Meyer" University Children's Hospital, 50139 Florence, Italy.
Arianna Carolina RosaDepartment of Scienza e Tecnologia del Farmaco, University of Turin, 10125 Turin, Italy.ORCID 0000-0002-6139-9241
Luca FilippiDivision of Neonatology and NICU, Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
University of Florence · ITMeyer Children's Hospital · ITUniversity of Bologna · ITUniversity of Pisa · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

β3-adrenoreceptor (β3-AR), a G-protein coupled receptor, has peculiar regulatory properties in response to oxygen and widespread localization. β3-AR is expressed in the most frequent neoplasms, also occurring in pregnant women, and its blockade reduces tumor growth, indicating β3-AR-blockers as a promising alternative to antineoplastic drugs during pregnancy. However, β3-AR involvement in prenatal morphogenesis and the consequences of its blockade for the fetus remain unknown. In this study, after the demonstrated expression of β3-AR in endothelial and smooth muscle cells of ductus arteriosus (DA), C57BL/6 pregnant mice were acutely treated at 18.5 of gestational day (GD) with indomethacin or with the selective β3-AR antagonist SR59230A, or chronically exposed to SR59230A from 15.5 to 18.5 GD. Six hours after the last treatment, fetuses were collected. Furthermore, newborn mice were treated straight after birth with BRL37344, a β3-AR agonist, and sacrificed after 7 h. SR59230A, at the doses demonstrated effective in reducing cancer progression (10 and 20 mg/kg) in acute and chronic mode, did not induce fetal DA constriction and did not impair the DA ability to close after birth, whereas at the highest dose (40 mg/kg), it was shown to cause DA constriction and preterm-delivery. BRL37344 administered immediately after birth did not alter the physiological DA closure.

Indexed as

Adrenergic beta-3 Receptor AntagonistsAnimalsAnimals, NewbornDisease Models, AnimalDisease ProgressionDuctus ArteriosusDuctus Arteriosus, PatentEthanolaminesFemaleIndomethacinMaleMaternal ExposureMiceMice, Inbred C57BLPregnancyPregnancy, Animal3-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalateAdrenergic beta-3 Receptor AntagonistsBRL 37344EthanolaminesIndomethacinPropanolaminesReceptors, Adrenergic, beta-3Receptors, G-Protein-Coupledcancerductus arteriosuspregnancyβ3-adrenorceptor

Identifiers

PMID33297453
PMCPMC7762377
OpenAlexW3111729396

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.