Evidence map›Paper›PMID 38385173›Full record

ArticleAmerican journal of physiology. Renal physiology2024

Human soluble prorenin receptor expressed in mouse renal collecting duct shows sex-specific effect on cardiorenal function.

Gertrude Arthur, Audrey Poupeau, Katherine Biel, Jeffrey L Osborn, Ming Gong, Terry D Hinds, Volkhard Lindner, Analia S Loria

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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.

Gertrude ArthurDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky, United States.ORCID 0000-0002-1850-1781
Audrey PoupeauDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky, United States.
Katherine BielDepartment of Nutrition and Dietetics, University of Kentucky, Lexington, Kentucky, United States.
Jeffrey L OsbornDepartment of Pathophysiology, Arkansas Colleges of Health Education, Fort Smith, Arkansas, United States.ORCID 0000-0002-2636-5345
Ming GongDepartment of Physiology, University of Kentucky, Lexington, Kentucky, United States.
Terry D HindsDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky, United States.ORCID 0000-0002-7599-1529
Volkhard LindnerMaineHealth Institute for Research, Scarborough, Maine, United States.
Analia S LoriaDepartment of Pharmacology and Nutritional Sciences, University of Kentucky, Lexington, Kentucky, United States.ORCID 0000-0002-9284-2146
University of Kentucky · USMaineHealth · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
The role of night shift work in metabolic disorders during and after pregnancyP20GM121301 · NIGMS · MAINEHEALTH · PI Lucy Liaw · 2017 to 2026
$25.1M
Pilot Projects ProgramP30GM127211 · NIGMS · UNIVERSITY OF KENTUCKY · PI CASSIS, LISA A · 2018 to 2022
$5.7M
The role of soluble prorenin receptor in hypertension associated with obesityR01HL142969 · NHLBI · UNIVERSITY OF KENTUCKY · PI LORIA, ANALIA · 2018 to 2021
$1.5M
NCATS NIH HHS UL1 TR001998NHLBI NIH HHS R01 HL142969NIGMS NIH HHS P20 GM121301NIGMS NIH HHS P30 GM127211
6 · The paper itself

Abstract

Soluble prorenin receptor (sPRR), a component of the renin-angiotensin system (RAS), has been identified as a plasma biomarker for hypertension and cardiovascular diseases in humans. Despite studies showing that sPRR in the kidney is produced by tubular cells in the renal collecting duct (CD), its biological actions modulating cardiorenal function in physiological conditions remain unknown. Therefore, the objective of our study was to investigate whether CD-derived human sPRR (HsPRR) expression influences cardiorenal function and examine sex and circadian differences. Thus, we investigated the status of the intrarenal RAS, water and electrolyte balance, renal filtration capacity, and blood pressure (BP) regulation in CD-HsPRR and control (CTL) mice. CD-HsPRR mice were generated by breeding human sPRR-Myc-tag mice with Hoxb7/Cre mice. Renal sPRR expression increased in CD-HsPRR mice, but circulating sPRR and RAS levels were unchanged compared with CTL mice. Only female littermates expressing CD-HsPRR showed

Indexed as

HypertensionVacuolar Proton-Translocating ATPasesAngiotensin IIAnimalsFemaleHumansKidneyMaleMiceProrenin ReceptorReceptors, Cell SurfaceReninRenin-Angiotensin SystemAngiotensin IIProrenin ReceptorReceptors, Cell SurfaceReninVacuolar Proton-Translocating ATPasescollecting ducthypertensionkidneyrenin-angiotensin systemsex differencessoluble prorenin receptorsPRR

Identifiers

PMID38385173
PMCPMC11208026
OpenAlexW4392052281

What OpenQuestion holds

Textmetadata
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.