Evidence map›Paper›PMID 34305630›Full record

ArticleFrontiers in physiology2021

Anti-apoptotic and Matrix Remodeling Actions of a Small Molecule Agonist of the Human Relaxin Receptor, ML290 in Mice With Unilateral Ureteral Obstruction.

Hooi Hooi Ng, Mariluz Soula, Bryan Rivas, Kenneth J Wilson, Juan J Marugan, Alexander I Agoulnik

Open access · goldAbstract read
In one paragraph

Article in Frontiers in physiology, 2021. 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
0.2field-weighted citation impact, top 42% 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, 2 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 1 country.

Hooi Hooi NgDepartment of Human and Molecular Genetics, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, United States.
Mariluz SoulaDepartment of Human and Molecular Genetics, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, United States.
Bryan RivasDepartment of Human and Molecular Genetics, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, United States.
Kenneth J WilsonNIH Chemical Genomics Center, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States.
Juan J MaruganNIH Chemical Genomics Center, National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, United States.
Alexander I AgoulnikDepartment of Human and Molecular Genetics, Herbert Wertheim College of Medicine, Florida International University, Miami, FL, United States.
Florida International University · USNational Center for Advancing Translational Sciences · USNational Institutes of Health · US

Funding

NIH MARC USTAR program and The Transdisciplinary Biomolecular and Biomedical Sciences (TBBS) Program at FIU supplement: Mentor-mentee alliancesT34GM083688 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI MILLS, DEETTA K · 2008 to 2023
$3.7M
Relaxin receptor agonists for treatment of liver fibrosisR01DK110167 · NIDDK · FLORIDA INTERNATIONAL UNIVERSITY · PI AGOULNIK, ALEXANDER I · 2017 to 2021
$2.0M
MARC U*STAR at Florida International UniversityT34GM154122 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI MILLS, DEETTA K · 2024 to 2024
$249k
NIDDK NIH HHS R01 DK110167NIGMS NIH HHS T34 GM083688NIGMS NIH HHS T34 GM154122
6 · The paper itself

Abstract

Diseases, such as diabetes and hypertension, often lead to chronic kidney failure. The peptide hormone relaxin has been shown to have therapeutic effects in various organs. In the present study, we tested the hypothesis that ML290, a small molecule agonist of the human relaxin receptor (RXFP1), is able to target the kidney to remodel the extracellular matrix and reduce apoptosis induced by unilateral ureteral obstruction (UUO). UUO was performed on the left kidney of humanized RXFP1 mice, where the right kidneys served as contralateral controls. Mice were randomly allocated to receive either vehicle or ML290 (30 mg/kg)

Indexed as

apoptosisextracellular matrixrelaxinrelaxin family peptide receptor 1unilateral ureteral obstruction

Identifiers

PMID34305630
PMCPMC8293094
OpenAlexW3182727832

What OpenQuestion holds

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LicenceCC BY
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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.