Evidence map›Paper›PMID 36204858›Full record

ArticleNeural regeneration research2023

Erythropoietin inhibits ferroptosis and ameliorates neurological function after spinal cord injury.

Yu Kang, Rui Zhu, Shuang Li, Kun-Peng Qin, Hao Tang, Wen-Shan Shan, Zong-Sheng Yin

Open access · goldAbstract read
In one paragraph

Article in Neural regeneration research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Review
  7. Article
  8. Review
  9. Ferroptosis: a new target for depression prevention and treatment.Journal of neural transmission (Vienna, Austria : 1996) · 2025
    Review
  10. Article
  11. Hypoxia-inducible factor-1 as targets for neuroprotection : from ferroptosis to Parkinson's disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Review
  12. Article
  13. Review
  14. Article
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  16. Article
  17. Article
  18. Neural regeneration research · 2024
    Review
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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

7 authors at 3 institutions in 2 countries.

Yu KangDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Rui ZhuDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Shuang LiDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Kun-Peng QinDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Hao TangDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Wen-Shan ShanDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Zong-Sheng YinDepartment of Orthopedics, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, China.
Creative Commons · USAnhui Medical University · CNFirst Affiliated Hospital of Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is one of the critical pathological events in spinal cord injury. Erythropoietin has been reported to improve the recovery of spinal cord injury. However, whether ferroptosis is involved in the neuroprotective effects of erythropoietin on spinal cord injury has not been examined. In this study, we established rat models of spinal cord injury by modified Allen's method and intraperitoneally administered 1000 and 5000 IU/kg erythropoietin once a week for 2 successive weeks. Both low and high doses of erythropoietin promoted recovery of hindlimb function, and the high dose of erythropoietin led to better outcome. High dose of erythropoietin exhibited a stronger suppressive effect on ferroptosis relative to the low dose of erythropoietin. The effects of erythropoietin on inhibiting ferroptosis-related protein expression and restoring mitochondrial morphology were similar to those of Fer-1 (a ferroptosis suppressor), and the effects of erythropoietin were largely diminished by RSL3 (ferroptosis activator). In vitro experiments showed that erythropoietin inhibited RSL3-induced ferroptosis in PC12 cells and increased the expression of xCT and Gpx4. This suggests that xCT and Gpx4 are involved in the neuroprotective effects of erythropoietin on spinal cord injury. Our findings reveal the underlying anti-ferroptosis role of erythropoietin and provide a potential therapeutic strategy for treating spinal cord injury.

Indexed as

erythropoietinferroptosisGpx4iron overloadlipid peroxidationmechanismneurological function recoveryspinal cord injuryspinal neuronxCT

Identifiers

PMID36204858
PMCPMC9700110
OpenAlexW4296955666

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.