Evidence map›Paper›PMID 28491480›Full record

ReviewNeural plasticity2017

New Treatment Strategies of Depression: Based on Mechanisms Related to Neuroplasticity.

Yu-Jhen Huang, Hsien-Yuan Lane, Chieh-Hsin Lin

Open access · goldAbstract readReview
In one paragraph

Review in Neural plasticity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
6.9field-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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 72 citations in OpenAlex.

  1. Pooled it
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  14. Dendritogenic Potential of the Ethanol Extract fromMolecules (Basel, Switzerland) · 2023
    Article
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  19. Depression in Sub-Saharan Africa.IBRO neuroscience reports · 2022
    Article
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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

3 authors at 3 institutions in 1 country.

Yu-Jhen HuangDepartment of Psychiatry and Brain Disease Research Center, China Medical University Hospital, Taichung, Taiwan.ORCID 0000-0003-0519-3350
Hsien-Yuan LaneDepartment of Psychiatry and Brain Disease Research Center, China Medical University Hospital, Taichung, Taiwan.
Chieh-Hsin LinGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.ORCID 0000-0001-6949-8968
Asia University · TWChang Gung University · TWChina Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder is a severe and complex mental disorder. Impaired neurotransmission and disrupted signalling pathways may influence neuroplasticity, which is involved in the brain dysfunction in depression. Traditional neurobiological theories of depression, such as monoamine hypothesis, cannot fully explain the whole picture of depressive disorders. In this review, we discussed new treatment directions of depression, including modulation of glutamatergic system and noninvasive brain stimulation. Dysfunction of glutamatergic neurotransmission plays an important role in the pathophysiology of depression. Ketamine, an N-methyl-D-aspartate (NMDA) receptor antagonist, has rapid and lasting antidepressive effects in previous studies. In addition to ketamine, other glutamatergic modulators, such as sarcosine, also show potential antidepressant effect in animal models or clinical trials. Noninvasive brain stimulation is another new treatment strategy beyond pharmacotherapy. Growing evidence has demonstrated that superficial brain stimulations, such as transcranial magnetic stimulation, transcranial direct current stimulation, cranial electrotherapy stimulation, and magnetic seizure therapy, can improve depressive symptoms. The antidepressive effect of these brain stimulations may be through modulating neuroplasticity. In conclusion, drugs that modulate neurotransmission via NMDA receptor and noninvasive brain stimulation may provide new directions of treatment for depression. Furthermore, exploring the underlying mechanisms will help in developing novel therapies for depression in the future.

Indexed as

Neuronal PlasticityAnimalsAntidepressive AgentsBrainClinical Trials as TopicDisease Models, AnimalDrug Partial AgonismElectroconvulsive TherapyHumansKetamineMajor Depressive DisorderReceptors, Metabotropic GlutamateReceptors, N-Methyl-D-AspartateSignal TransductionSynaptic TransmissionTranscranial Direct Current StimulationAntidepressive AgentsKetamineNR2B NMDA receptorReceptors, Metabotropic GlutamateReceptors, N-Methyl-D-Aspartate

Identifiers

PMID28491480
PMCPMC5405587
OpenAlexW2605978316

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.