Evidence map›Paper›PMID 29873589›Full record

ArticleThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society2018

Acute and Chronic Iron Overloading Differentially Modulates the Expression of Cellular Iron-homeostatic Molecules in Normal Rat Kidney.

Bassem Refaat, Abdelghany Hassan Abdelghany, Mohammad A BaSalamah, Mohamed El-Boshy, Jawwad Ahmad, Shakir Idris

Abstract read
In one paragraph

Article in The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Amelioration of nephrotoxicity by targeting ferroptosis: role of NCOA4, IREB2, and SLC7a11 signaling.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Article
  6. Article
  7. Animal models of kidney iron overload and ferroptosis: a review of the literature.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2023
    Review
  8. Mitochondrial Regulation of Ferroptosis in Cancer Therapy.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Review
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  13. Article
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  17. Antioxidative and Anti-Inflammatory Protective Effects ofOxidative medicine and cellular longevity · 2022
    Article
  18. Effects of supraphysiological vitamin DHistochemistry and cell biology · 2021
    Article
  19. Article
  20. 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

6 authors at 2 institutions in 4 countries.

Bassem RefaatLaboratory Medicine Department, Faculty of Applied Medical Sciences.ORCID 0000-0003-4267-1016
Abdelghany Hassan AbdelghanyLaboratory Medicine Department, Faculty of Applied Medical Sciences.
Mohammad A BaSalamahLaboratory Medicine Department, Faculty of Applied Medical Sciences.
Mohamed El-BoshyDepartment of Clinical Pathology, Faculty of Veterinary Medicine, Mansoura University, Mansoura, Egypt.
Jawwad AhmadLaboratory Medicine Department, Faculty of Applied Medical Sciences.
Shakir IdrisLaboratory Medicine Department, Faculty of Applied Medical Sciences.
Applied Science Private University · JOMansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about the renal responses to acute iron overloading. This study measured the renal tubular expression of transferrin receptor-1 (TfR1), cubilin/megalin receptors, hepcidin, ferroportin, and ferritin chains following subacute intoxication of 40 male Wistar rats with a single oral dose of ferrous iron (300 mg/kg). The animals were randomly subdivided into 4 equal subgroups at the time of necropsy (1, 2, 4, and 8 hr). The results were compared with the controls ( n=15) and with the chronic group ( n=15), which received iron for 4 weeks (75 mg/kg/day; 5 days/week). Although both toxicity models inhibited TfR1, they upregulated the cubilin/megalin receptors and hepcidin, and triggered iron deposition in tubular cells. The ferritin heavy-chain and ferroportin were downregulated in the 2-hr and 4-hr acute subgroups, whereas chronic toxicity promoted their expression, compared with controls. Moreover, the 4-hr and 8-hr subgroups had higher intracellular Fe

Indexed as

Acute DiseaseAnimalsApoptosisCaspasesChronic DiseaseEnzyme-Linked Immunosorbent AssayFerritinsFluorescent Antibody TechniqueHepcidinsIronIron OverloadKidneyLow Density Lipoprotein Receptor-Related Protein-2MaleOxidative StressRats, WistarCaspasesFerritinsHepcidinsintrinsic factor-cobalamin receptorIronLow Density Lipoprotein Receptor-Related Protein-2Receptors, Cell SurfaceReceptors, TransferrinTfrc protein, ratcubilinferritinferroportinhepcidinmegalinoxidative stress and ferroptosistransferrin receptor-1

Identifiers

PMID29873589
PMCPMC6213567
OpenAlexW2805133572

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.