Evidence map›Paper›PMID 27164096›Full record

ReviewInternational journal of molecular sciences2016

Erythropoietin Pathway: A Potential Target for the Treatment of Depression.

Chongyang Ma, Fafeng Cheng, Xueqian Wang, Changming Zhai, Wenchao Yue, Yajun Lian, Qingguo Wang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  15. Review
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  17. Review
  18. Erythropoietin Induces Homeostatic Plasticity at Hippocampal Synapses.Cerebral cortex (New York, N.Y. : 1991) · 2018
    Article
  19. Review
  20. Neuroprogression: the hidden mechanism of depression.Neuropsychiatric disease and treatment · 2018
    Review
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 1 institution in 1 country.

Chongyang MaSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. machongyang@live.com.
Fafeng ChengSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. fafengcheng@gmail.com.
Xueqian WangSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. shirlyding@163.com.
Changming ZhaiSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. zhaichangming1989@163.com.
Wenchao YueSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. yuewenchao@bucm.edu.cn.
Yajun LianSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. niangkuosir@bucm.edu.cn.
Qingguo WangSchool of Basic Medical Sciences, Beijing University of Chinese Medicine, School of Basic Medical Sciences, 11 Beisanhuandong Road, Chao Yang District, Beijing 100029, China. 642006@bucm.edu.cn.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past decade, accumulating evidence from both clinical and experimental studies has indicated that erythropoietin may have antidepressant effects. In addition to the kidney and liver, many organs have been identified as secretory tissues for erythropoietin, including the brain. Its receptor is expressed in cerebral and spinal cord neurons, the hypothalamus, hippocampus, neocortex, dorsal root ganglia, nerve axons, and Schwann cells. These findings may highlight new functions for erythropoietin, which was originally considered to play a crucial role in the progress of erythroid differentiation. Erythropoietin and its receptor signaling through JAK2 activate multiple downstream signaling pathways including STAT5, PI3K/Akt, NF-κB, and MAPK. These factors may play an important role in inflammation and neuroprogression in the nervous system. This is particularly true for the hippocampus, which is possibly related to learning, memory, neurocognitive deficits and mood alterations. Thus, the influence of erythropoietin on the downstream pathways known to be involved in the treatment of depression makes the erythropoietin-related pathway an attractive target for the development of new therapeutic approaches. Focusing on erythropoietin may help us understand the pathogenic mechanisms of depression and the molecular basis of its treatment.

Indexed as

AnimalsAntidepressive AgentsDepressionErythropoietinHippocampusHumansSignal TransductionAntidepressive AgentsErythropoietinanti-depressant targetsdepressiondrug treatmentEPOerythropoietinhippocampalmajor depressive disordersignaling pathway

Identifiers

PMID27164096
PMCPMC4881503
OpenAlexW2346203535

What OpenQuestion holds

Textmetadata
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.