Evidence map›Paper›PMID 24116080›Full record

ArticlePloS one2013

Increased renal iron accumulation in hypertensive nephropathy of salt-loaded hypertensive rats.

Yoshiro Naito, Hisashi Sawada, Makiko Oboshi, Aya Fujii, Shinichi Hirotani, Toshihiro Iwasaku, Yoshitaka Okuhara, Akiyo Eguchi, Daisuke Morisawa, Mitsumasa Ohyanagi and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The Cross-Link between Ferroptosis and Kidney Diseases.Oxidative medicine and cellular longevity · 2021
    Review
  5. Overview of iron metabolism in health and disease.Hemodialysis international. International Symposium on Home Hemodialysis · 2017
    Review
  6. Attenuation of hypertension and renal damage in renovascular hypertensive rats by iron restriction.Hypertension research : official journal of the Japanese Society of Hypertension · 2016
    Article
  7. Association between renal iron accumulation and renal interstitial fibrosis in a rat model of chronic kidney disease.Hypertension research : official journal of the Japanese Society of Hypertension · 2015
    Article
  8. 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

12 authors at 2 institutions in 1 country.

Yoshiro NaitoCardiovascular Division, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Japan.
Hisashi Sawada
Makiko Oboshi
Aya Fujii
Shinichi Hirotani
Toshihiro Iwasaku
Yoshitaka Okuhara
Akiyo Eguchi
Daisuke Morisawa
Mitsumasa Ohyanagi
Takeshi Tsujino
Tohru Masuyama
Hyogo Medical University · JPHyogo University of Health Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although iron is reported to be associated with the pathogenesis of chronic kidney disease, it is unknown whether iron participates in the pathophysiology of nephrosclerosis. Here, we investigate whether iron is involved in the development of hypertensive nephropathy and the effects of iron restriction on nephrosclerosis in salt- loaded stroke-prone spontaneously hypertensive rats (SHRSP). SHRSP were given either a normal or high-salt diet for 8 weeks. Another subset of SHRSP were fed a high-salt with iron-restricted diet. SHRSP given a high-salt diet developed severe hypertension and nephrosclerosis. As a result, survival rate was decreased after 8 weeks diet. Importantly, massive iron accumulation and increased iron content were observed in the kidneys of salt-loaded SHRSP, along with increased superoxide production, urinary 8-Hydroxy-2'-deoxyguanosine excretion, and urinary iron excretion; however, these changes were markedly attenuated by iron restriction. Of interest, expression of cellular iron transport proteins, transferrin receptor 1 and divalent metal transporter 1, was increased in the tubules of salt-loaded SHRSP. Notably, iron restriction attenuated the development of severe hypertension and nephrosclerosis, thereby improving survival rate in salt-loaded SHRSP. Taken together, these results suggest a novel mechanism by which iron plays a role in the development of hypertensive nephropathy and establish the effects of iron restriction on salt-induced nephrosclerosis.

Indexed as

AnimalsBlood PressureCation Transport ProteinsHypertension, RenalIronKidneyMaleNephritisNephrosclerosisRatsRats, Inbred SHRReceptors, TransferrinSodium Chloride, DietarySolute Carrier Family 11, Member 2Cation Transport ProteinsIronReceptors, TransferrinSodium Chloride, DietarySolute Carrier Family 11, Member 2Tfrc protein, rat

Identifiers

PMID24116080
PMCPMC3792990
OpenAlexW1994247883

What OpenQuestion holds

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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.