Evidence map›Paper›PMID 34676684›Full record

ArticlePhysiological reports2021

β3 adrenergic receptor as potential therapeutic target in ADPKD.

Giorgia Schena, Monica Carmosino, Samantha Chiurlia, Laura Onuchic, Mauro Mastropasqua, Eugenio Maiorano, Francesco P Schena, Michael J Caplan

Open access · goldAbstract read
In one paragraph

Article in Physiological reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. GPCR Sense Communication Among Interaction Nematodes with Other Organisms.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Review
  6. The βAdvances in pharmacological and pharmaceutical sciences · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Polycystic kidney disease strikes a nerve.Physiological reports · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Giorgia SchenaDepartment of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0001-5504-4834
Monica CarmosinoDepartment of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0001-7600-8816
Samantha ChiurliaSchena Foundation, Valenzano, Italy.
Laura OnuchicDepartment of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.
Mauro MastropasquaDepartment of Emergency and Organ Transplantation, Section of Pathological Anatomy, University of Bari, Bari, Italy.ORCID 0000-0002-8306-0839
Eugenio MaioranoDepartment of Emergency and Organ Transplantation, Section of Pathological Anatomy, University of Bari, Bari, Italy.ORCID 0000-0002-0472-5338
Francesco P SchenaSchena Foundation, Valenzano, Italy.ORCID 0000-0001-7927-5207
Michael J CaplanDepartment of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut, USA.ORCID 0000-0001-5768-4405
Yale University · USInternational Centre for Advanced Mediterranean Agronomic Studies · ITUniversity of Bari Aldo Moro · ITUniversity of Basilicata · IT

Funding

Renal Physiology and Phenotyping CoreP30DK079310 · NIDDK · YALE UNIVERSITY · PI ARONSON, PETER S. · 2008 to 2022
$16.8M
Pathways and Partners in Renal Epithelial Cell PolarityR01DK072614 · NIDDK · YALE UNIVERSITY · PI CAPLAN, MICHAEL J. · 2005 to 2022
$6.9M
In vivo Pathway Discovery in Autosomal Dominant Polycystic Kidney DiseaseRC2DK120534 · NIDDK · YALE UNIVERSITY · PI CAPLAN, MICHAEL J., SHULMAN, GERALD I · 2019 to 2023
$6.6M
NIDDK NIH HHS P30 DK079310NIDDK NIH HHS R01 DK072614NIDDK NIH HHS RC2 DK120534
6 · The paper itself

Abstract

Autosomal dominant polycystic kidney disease (ADPKD) disrupts renal parenchyma through progressive expansion of fluid-filled cysts. The only approved pharmacotherapy for ADKPD involves the blockade of the vasopressin type 2 receptor (V2R). V2R is a GPCR expressed by a subset of renal tubular cells and whose activation stimulates cyclic AMP (cAMP) accumulation, which is a major driver of cyst growth. The β3-adrenergic receptor (β3-AR) is a GPCR expressed in most segments of the murine nephron, where it modulates cAMP production. Since sympathetic nerve activity, which leads to activation of the β3-AR, is elevated in patients affected by ADPKD, we hypothesize that β3-AR might constitute a novel therapeutic target. We find that administration of the selective β3-AR antagonist SR59230A to an ADPKD mouse model (Pkd1

Indexed as

Adrenergic beta-3 Receptor AntagonistsAnimalsCase-Control StudiesCell ProliferationCells, CulturedCyclic AMPEpithelial CellsHumansKidneyMaleMiceMice, KnockoutPolycystic Kidney, Autosomal DominantPropanolaminesReceptors, Adrenergic, beta-33-(2-ethylphenoxy)-1-(1,2,3,4-tetrahydronaphth-1-ylamino)-2-propanol oxalateAdrenergic beta-3 Receptor AntagonistsCyclic AMPPropanolaminesReceptors, Adrenergic, beta-3autosomal dominant polycystic kidney diseaseG protein-coupled receptorsSR59230Aβ-adrenergic receptors

Identifiers

PMID34676684
PMCPMC8531837
OpenAlexW3205164352

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.