Evidence map›Paper›PMID 30557385›Full record

ArticlePloS one2018

Cholinesterase inhibitor rivastigmine enhances nerve growth factor-induced neurite outgrowth in PC12 cells via sigma-1 and sigma-2 receptors.

Kazuki Terada, Keisuke Migita, Yukari Matsushima, Yumi Sugimoto, Chiaki Kamei, Taichi Matsumoto, Masayoshi Mori, Kazuhisa Matsunaga, Jiro Takata, Yoshiharu Karube

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Screening of σJournal of medicinal chemistry · 2022
    Article
  13. Review
  14. Review
  15. Sigma receptors and neurological disorders.Pharmacological reports : PR · 2021
    Review
  16. Article
  17. Review
  18. Article
  19. 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

10 authors at 3 institutions in 1 country.

Kazuki TeradaDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.ORCID 0000-0003-0257-5812
Keisuke MigitaDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Yukari MatsushimaFaculty of Pharmaceutical Sciences, Yasuda Women's University, Hiroshima, Japan.
Yumi SugimotoFaculty of Pharmaceutical Sciences, Himeji Dokkyo University, Hyogo, Japan.
Chiaki KameiFaculty of Pharmaceutical Sciences, Yasuda Women's University, Hiroshima, Japan.
Taichi MatsumotoDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Masayoshi MoriDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Kazuhisa MatsunagaDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Jiro TakataDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Yoshiharu KarubeDepartment of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Fukuoka University · JPYasuda Women's University · JPHimeji Dokkyo University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rivastigmine (Riv) is a potent and selective cholinesterase (acetylcholinesterase, AChE and butyrylcholinesterase, BuChE) inhibitor developed for the treatment of Alzheimer's disease (AD). To elucidate whether Riv causes neuronal differentiation, we examined its effect on nerve growth factor (NGF)-induced neurite outgrowth in PC12 cells. At concentrations of 0-100 μM, Riv was non-toxic in PC12 cells. Riv caused dose-dependent (10-100 μM) enhancement of NGF-induced neurite outgrowth, which was completely inhibited by the TrkA antagonist GW-441756. By contrast, Riv-mediated enhancement of neurite outgrowth was not blocked by the acetylcholine receptor antagonists, scopolamine and hexamethonium. However, the sigma-1 receptor (Sig-1R) antagonist NE-100 and sigma-2 receptor (Sig-2R) antagonist SM-21 each blocked about half of the Riv-mediated enhancement of NGF-induced neurite outgrowth. Interestingly, the simultaneous application of NE-100 and SM-21 completely blocked the enhancement of NGF-induced neurite outgrowth by Riv. These findings suggest that both Sig-1R and Sig-2R play important roles in NGF-induced neurite outgrowth through TrkA and that Riv may contribute to neuronal repair via Sig-1R and Sig-2R in AD therapy.

Indexed as

AnimalsCell SurvivalCholinesterase InhibitorsDose-Response Relationship, DrugMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Nerve Growth FactorNeurogenesisNeuronal OutgrowthNeurotransmitter AgentsPC12 CellsProto-Oncogene Proteins c-aktRatsReceptors, CholinergicReceptors, sigmaRivastigmineCholinesterase InhibitorsMapk1 protein, ratMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Nerve Growth FactorNeurotransmitter AgentsProto-Oncogene Proteins c-aktReceptors, CholinergicReceptors, sigmaRivastigmineSigma-1 Receptorsigma-2 receptor

Identifiers

PMID30557385
PMCPMC6296549
OpenAlexW2905154903

What OpenQuestion holds

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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.