Evidence map›Paper›PMID 35053120›Full record

ArticleBiology2022

Iron Inhibits the Translation and Activity of the Renal Epithelial Sodium Channel.

Abdel A Alli, Ling Yu, Ewa Wlazlo, Sadat Kasem, Mohammed F Gholam, Dhruv Desai, Carlos I Lugo, Sophie Vaulont, Yogesh M Scindia

Open access · goldAbstract read
In one paragraph

Article in Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 4 institutions in 3 countries.

Abdel A AlliDepartment of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Ling YuDepartment of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Ewa WlazloDivision of Nephrology, Department of Medicine, University of Virginia, Charlottesville, VA 22904, USA.
Sadat KasemDivision of Nephrology, Hypertension, and Renal Transplantation, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Mohammed F GholamDepartment of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Dhruv DesaiDivision of Nephrology, Hypertension, and Renal Transplantation, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Carlos I LugoDepartment of Physiology and Functional Genomics, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
Sophie VaulontInstitut Cochin, Universite' de Paris, INSERM U1016, 75014 Paris, France.
Yogesh M ScindiaDivision of Nephrology, Hypertension, and Renal Transplantation, Department of Medicine, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
University of Florida · USInserm · FRKing Saud bin Abdulaziz University for Health Sciences · SAUniversity of Virginia · US

Funding

The circadian clock protein BMAL and post-translational regulation of ENaC in the kidneyR01DK123078 · NIDDK · UNIVERSITY OF FLORIDA · PI ALLI, ABDEL AYUBE · 2020 to 2024
$1.7M
NIDDK NIH HHS R01 DK123078
6 · The paper itself

Abstract

Hypertension is associated with an increased renal expression and activity of the epithelial sodium channel (ENaC) and iron deficiency. Distal tubules absorb iron, causing perturbations that may influence local responses. In this observational study, we investigated the relationship between iron content and ENaC expression and activity using two cell lines and hepcidin knockout mice (a murine model of iron overload). We found that iron did not transcriptionally regulate ENaC in hepcidin knockout mice or in vitro in collecting duct cells. However, the renal tubules of hepcidin knockout mice have a lower expression of ENaC protein. ENaC activity in cultured Xenopus 2F3 cells and mpkCCD cells was inhibited by iron, which could be reversed by iron chelation. Thus, our novel findings implicate iron as a regulator of ENaC protein and its activity.

Indexed as

anemiaENaChypertensionironsalt loading

Identifiers

PMID35053120
PMCPMC8772986
OpenAlexW4206330578

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.