Evidence map›Paper›PMID 30361820›Full record

ArticleFish physiology and biochemistry2019

Hepcidin protects against iron overload-induced inhibition of bone formation in zebrafish.

Yu Jiang, Bin Chen, Yilin Yan, Guo-Xing Zhu

Abstract read
PubMed Publisher
In one paragraph

Article in Fish physiology and biochemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 33 citations in OpenAlex.

  1. Bone phenotyping of murine hemochromatosis models with deficiencies of Hjv, Alk2, or Alk3: The influence of sex and the bone compartment.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  2. Article
  3. The influence of iron on bone metabolism disorders.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2024
    Review
  4. Article
  5. Noncoding RNAs: the crucial role of programmed cell death in osteoporosis.Frontiers in cell and developmental biology · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. 1,25(OH)International journal of molecular sciences · 2021
    Article
  11. Review
  12. Fish Models of Induced Osteoporosis.Frontiers in cell and developmental biology · 2021
    Review
  13. 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

4 authors at 4 institutions in 2 countries.

Yu JiangDepartment of Orthopedics, Nanjing Medical University Affiliated Wuxi Second Hospital, Wuxi, 214000, China.
Bin ChenDepartment of Orthopedics, The Second Affiliated Hospital of Soochow University, 1055 Sanxiang Road, Suzhou, 215004, China.
Yilin YanInstitute of Neuroscience, University of Oregon, Eugene, OR, USA.
Guo-Xing ZhuDepartment of Orthopedics, Nanjing Medical University Affiliated Wuxi Second Hospital, Wuxi, 214000, China. guoxing-zhu@163.com.
Nanjing Medical University · CNSecond Affiliated Hospital of Soochow University · CNSecond Hospital of Shanxi Medical University · CNUniversity of Oregon · US

Funding

Jiangsu Province Special Medical Grant BL2014044Jiangsu Youth Medical Foundation of China QNRC2016149National Advance Natural Science Foundation of China SDFEGJ1601Suzhou Clinical Key Special Diseases Fund LCZX210305the National Natural Science Foundation of China 81602864
6 · The paper itself

Abstract

Iron overload increases the risk of osteoporosis, which leads to an increase in the incidences of bone fracture after menopause. In vitro studies have demonstrated that excess iron can inhibit osteoblast activity. Hepcidin, a central regulator of iron homeostasis, prevents iron overload, and thus, it is considered to have anti-osteoporosis effects. In this study, a zebrafish model was employed to investigate the therapeutic role of hepcidin in iron overload-induced inhibition of bone formation. Our results show that ferric ammonium citrate (FAC) treatment decreased osteoblast-specific gene expression (runx2a, runx2b, and bglap) and bone mineralization in the zebrafish embryo, accompanied with increased whole-body iron levels and oxidative stress. Bone mineralization and osteoblast-specific gene expression increased with the microinjection of hepcidin-flag Capped-mRNA into zebrafish embryos. Moreover, the whole-body iron content and oxidative stress in the iron-overloaded zebrafish embryos decreased when microinjection of hepcidin preceded the FAC treatment. Therefore, our study suggests that hepcidin could prevent and rescue reduced bone formation caused by FAC treatment by preventing iron absorption.

Indexed as

AnimalsAnti-Infective AgentsBone DevelopmentDose-Response Relationship, DrugDown-RegulationFerric CompoundsGene Expression RegulationHepcidinsIron OverloadOsteoblastsQuaternary Ammonium CompoundsZebrafishAnti-Infective Agentsferric ammonium citrateFerric CompoundsHepcidinsQuaternary Ammonium CompoundsBone formationHepcidinIron overloadOsteoblastOxidative stressZebrafish

Identifiers

PMID30361820
OpenAlexW2898524969

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.