Evidence map›Paper›PMID 31820273›Full record

ArticleNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2020

FG-4592 Improves Depressive-Like Behaviors through HIF-1-Mediated Neurogenesis and Synapse Plasticity in Rats.

Gaifen Li, Ming Zhao, Xiang Cheng, Tong Zhao, Zhenlong Feng, Yongqi Zhao, Ming Fan, Lingling Zhu

Open access · bronzeAbstract read
In one paragraph

Article in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 3 pooled it
2.5field-weighted citation impact, top 10% 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

44 citing papers in PubMed, 3 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Pharmacological modulation of HIF-1 in the treatment of neuropsychiatric disorders.Journal of neural transmission (Vienna, Austria : 1996) · 2023
    Review
  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

8 authors at 3 institutions in 1 country.

Gaifen Li *Institute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China.
Ming Zhao *Institute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China.
Xiang ChengInstitute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China.
Tong ZhaoInstitute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China.
Zhenlong FengInstitute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China.
Yongqi ZhaoInstitute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China.
Ming FanInstitute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China. fanmingchina@126.com.
Lingling ZhuInstitute of Military Cognition and Brain Sciences, Academy of Military Medical Sciences, Beijing, 100850, China. linglingzhu@hotmail.com.ORCID http://orcid.org/0000-0002-2220-2231
Academy of Military Medical Sciences · CNCapital Medical University · CNNantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression, plus the accompanying memory impairment, is one of the leading causes of disability worldwide. Thus, there is a critical need to develop new drugs based on distinct strategies. FG-4592, an inhibitor of prolyl hydroxylase, activates the hypoxia-inducible factor-1 (HIF-1) pathway, to produce multiple effects on cell properties. Here, we examined whether FG-4592 has antidepressant effects, using a chronic unpredictable mild stress (CUMS) procedure to establish rodent depression models. We found that FG-4592 not only reversed depressive behaviors but also improved CUMS-induced memory impairment. Mechanistically, FG-4592 could play an important role in promoting hippocampal neurogenesis and synaptic plasticity. At the molecular level, FG-4592 was found to activate HIF-1 and cAMP-responsive element-binding protein/brain-derived neurotrophic factor signaling pathways in vivo, as well as promote the expression of postsynaptic density (PSD) proteins, PSD95 and Homer1. An examination of primary hippocampal neurons showed that FG-4592 promoted dendritic growth. Taken together, our results not only provide an experimental basis for the future application of FG-4592 in clinical treatment of depression but also support the argument that the HIF-1 signaling pathway is a promising target for the treatment of depression.

Indexed as

AnimalsAntidepressive AgentsBehavior, AnimalDepressionGlycineHippocampusHypoxia-Inducible Factor 1IsoquinolinesMaleNeurogenesisNeuronal PlasticityRatsRats, Sprague-DawleyStress, PsychologicalAntidepressive AgentsGlycineHypoxia-Inducible Factor 1IsoquinolinesroxadustatCUMSFG-4592HIF-1NeurogenesisSynapse plasticity

Identifiers

PMID31820273
PMCPMC7283439
OpenAlexW2992326296

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.