Evidence map›Paper›PMID 28990373›Full record

ArticleCNS neuroscience & therapeutics2017

Sigma-1 receptor agonist increases axon outgrowth of hippocampal neurons via voltage-gated calcium ions channels.

Dong Li, Shu-Zhuo Zhang, Yu-Hong Yao, Yun Xiang, Xiao-Yun Ma, Xiao-Li Wei, Hai-Tao Yan, Xiao-Yan Liu

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  11. Structural basis for σNature structural & molecular biology · 2018
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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

8 authors at 3 institutions in 2 countries.

Dong LiDepartment of Biochemical Pharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Shu-Zhuo ZhangDepartment of Biochemical Pharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Yu-Hong YaoState Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yun XiangTraining bases, Hunan Key Laboratory of Chinese Materia Medical Power and Innovative Drugs Established by Provincial and Ministry, Hunan University of Chinese Medicine, Changsha, China.
Xiao-Yun MaDepartment of Biochemical Pharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Xiao-Li WeiDepartment of Biochemical Pharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Hai-Tao YanDepartment of Biochemical Pharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Xiao-Yan LiuDepartment of Biochemical Pharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.ORCID http://orcid.org/0000-0003-4124-9358
Beijing Institute of Petrochemical Technology · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNHunan University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSigma-1 receptors (Sig-1Rs) are unique endoplasmic reticulum proteins that have been implicated in both neurodegenerative and ischemic diseases, such as Alzheimer's disease and stroke. Accumulating evidence has suggested that Sig-1R plays a role in neuroprotection and axon outgrowth. The underlying mechanisms of Sig-1R-mediated neuroprotection have been well elucidated. However, the mechanisms underlying the effects of Sig-1R on axon outgrowth are not fully understood.

methodsTo clarify this issue, we utilized immunofluorescence to compare the axon lengths of cultured naïve hippocampal neurons before and after the application of the Sig-1R agonist, SA4503. Then, electrophysiology and immunofluorescence were used to examine voltage-gated calcium ion channel (VGCCs) currents in the cell membranes and growth cones.

resultsWe found that Sig-1R activation dramatically enhanced the axonal length of the naïve hippocampal neurons. Application of the Sig-1R antagonist NE100 and gene knockdown techniques both demonstrated the effects of Sig-1R. The growth-promoting effect of SA4503 was accompanied by the inhibition of voltage-gated Ca

conclusionSig-1R activation can enhance axon outgrowth and may have a substantial influence on neurogenesis and neurodegenerative diseases.

Indexed as

NeuronsAnalysis of VarianceAnimalsAnimals, NewbornAnisolesAxonsCalcium Channel BlockersCalcium ChannelsCells, CulturedDose-Response Relationship, DrugFemaleHippocampusMaleMembrane PotentialsMorpholinesNeurites2-(4-morpholino)ethyl-1-phenylcyclohexane-1-carboxylateAnisolesCalcium Channel BlockersCalcium ChannelsMorpholinesN,N-dipropyl-2-(4-methoxy-3-(2-phenylethoxy)phenyl)ethylamine monohydrochlorideNootropic AgentsPiperazinesPropylaminesReceptors, sigmaSA 4503Sigma-1 ReceptorTubb3 protein, ratTubulinaxon outgrowthgrowth conehippocampal neuronssigma-1 receptorvoltage-gated calcium ions channels

Identifiers

PMID28990373
PMCPMC6492695
OpenAlexW2762815035

What OpenQuestion holds

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Registered trials

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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.