Evidence map›Paper›PMID 35269657›Full record

ArticleInternational journal of molecular sciences2022

Impact of Two Neuronal Sigma-1 Receptor Modulators, PRE084 and DMT, on Neurogenesis and Neuroinflammation in an Aβ

Emőke Borbély, Viktória Varga, Titanilla Szögi, Ildikó Schuster, Zsolt Bozsó, Botond Penke, Lívia Fülöp

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 27 citations in OpenAlex.

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  4. Glial Cells in Behavioral and Psychological Symptoms of Alzheimer's Disease.International journal of molecular sciences · 2026
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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

7 authors at 1 institution in 1 country.

Emőke BorbélyDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.
Viktória VargaDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.
Titanilla SzögiDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.ORCID 0000-0002-9854-7340
Ildikó SchusterDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.
Zsolt BozsóDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.ORCID 0000-0002-5713-3096
Botond PenkeDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.
Lívia FülöpDepartment of Medical Chemistry, University of Szeged, Dóm Tér 8, H-6720 Szeged, Hungary.ORCID 0000-0002-8010-0129
University of Szeged · HU

Funding

Hungarian Brain Research Program I KTIA_13_NAP-A-III/7National Research, Development, and Innovation Office, Hungary GINOP-2.3.2-15-2016-00060
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common form of dementia characterized by cognitive dysfunctions. Pharmacological interventions to slow the progression of AD are intensively studied. A potential direction targets neuronal sigma-1 receptors (S1Rs). S1R ligands are recognized as promising therapeutic agents that may alleviate symptom severity of AD, possibly via preventing amyloid-β-(Aβ-) induced neurotoxicity on the endoplasmic reticulum stress-associated pathways. Furthermore, S1Rs may also modulate adult neurogenesis, and the impairment of this process is reported to be associated with AD. We aimed to investigate the effects of two S1R agonists, dimethyltryptamine (DMT) and PRE084, in an Aβ-induced in vivo mouse model characterizing neurogenic and anti-neuroinflammatory symptoms of AD, and the modulatory effects of S1R agonists were analyzed by immunohistochemical methods and western blotting. DMT, binding moderately to S1R but with high affinity to 5-HT receptors, negatively influenced neurogenesis, possibly as a result of activating both receptors differently. In contrast, the highly selective S1R agonist PRE084 stimulated hippocampal cell proliferation and differentiation. Regarding neuroinflammation, DMT and PRE084 significantly reduced Aβ

Indexed as

Alzheimer DiseaseReceptors, sigmaAmyloid beta-PeptidesAnimalsDisease Models, AnimalMiceNeurogenesisNeuroinflammatory DiseasesN,N-DimethyltryptaminePeptide FragmentsSigma-1 ReceptorAmyloid beta-Peptidesamyloid beta-protein (1-42)N,N-DimethyltryptaminePeptide FragmentsReceptors, sigmaSigma-1 ReceptorAlzheimer’s diseaseAβ1–42-induce mouse modeldimethyltryptamineneurogenesisneuroinflammationPRE084sigma-1 receptor

Identifiers

PMID35269657
PMCPMC8910266
OpenAlexW4214690845

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.