Evidence map›Paper›PMID 30863710›Full record

Article3 Biotech2019

Erythropoietin protects neurons from apoptosis via activating PI3K/AKT and inhibiting Erk1/2 signaling pathway.

Wei Si, Jianyi Wang, Mei Li, Hao Qu, Ran Gu, Rui Liu, Lu Wang, Shirong Li, Xiao Hu

Open access · bronzeAbstract read
In one paragraph

Article in 3 Biotech, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.9field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Erythropoietin in Glaucoma: From Mechanism to Therapy.International journal of molecular sciences · 2023
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. AT1R/GSK-3Oxidative medicine and cellular longevity · 2020
    Article
  15. 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 1 institution in 1 country.

Wei SiDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Jianyi WangDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Mei LiDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Hao QuDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Ran GuDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Rui LiuDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Lu WangDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Shirong LiDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Xiao HuDepartment of Neurology, Guizhou Provincial People's Hospital, 83 Dongshan Road, Guizhou, 550000 China.
Guizhou Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to explore the neuroprotective effect and the underlying mechanism of erythropoietin (EPO) on the cortical neuronal cells insulted with oxygen and glucose deprivation (OGD). Different concentrations of EPO were used to determine the anti-apoptosis effect of EPO. In addition, PI3K inhibitor LY294002 and ERK1/2 inhibitor U0126 were added to explore the underlying mechanism of EPO. Cell apoptosis rate was measured by flow cytometry. The protein expression of Bax, Bcl-2, cleaved caspase-3, AKT, p-AKT, Erk1/2 and p-Erk1/2 wasmeasured by Western blot. Our results showed that EPO alleviates OGD-induced cell apoptosis in a dose-dependent manner; the neuroprotective effect of EPO was further confirmed by the fact that EPO treatment reversed the protein expression of cleaved caspase-3, as well as the Bcl-2/Bax ratio as compared with the OGD treatment. In the mechanism part, our results demonstrated that OGD and EPO nearly had no influence on the protein expression of AKT and Erk1/2 but altered the phosphorylation of them. Specifically, OGD decreased the expression of p-AKT and increased the expression of p-Erk1/2; while, EPO treatment reversed the expression of p-AKT and p-Erk1/2 as compared with OGD treatment. Interestingly, LY294002 decreased the expression of p-AKT and attenuated the neuroprotective effect of EPO; while, U0126 decreased the expression of p-Erk1/2 and enhanced the neuroprotective effect of EPO. Our study demonstrated that EPO protects neurons against apoptosis induced by OGD, which is closely related with activation of PI3K/AKT and inactivation of Erk1/2 signaling pathway.

Indexed as

Erk1/2ErythropoietinNeuroprotective agentsPI3K/AKT

Identifiers

PMID30863710
PMCPMC6405787
OpenAlexW2922117972

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.