Evidence map›Paper›PMID 35743175›Full record

ArticleInternational journal of molecular sciences2022

EST79232 and EST79376, Two Novel Sigma-1 Receptor Ligands, Exert Neuroprotection on Models of Motoneuron Degeneration.

Núria Gaja-Capdevila, Neus Hernández, Sandra Yeste, Raquel F Reinoso, Javier Burgueño, Ana Montero, Manuel Merlos, José M Vela, Mireia Herrando-Grabulosa, Xavier Navarro

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Imaging diagnosis in peripheral nerve injury.Frontiers in neurology · 2023
    Review
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 1 institution in 1 country.

Núria Gaja-CapdevilaDepartment of Cell Biology, Physiology and Immunology, Institute of Neurosciences, Universitat Autònoma de Barcelona, 01893 Bellaterra, Spain.ORCID 0000-0002-0028-570X
Neus HernándezDepartment of Cell Biology, Physiology and Immunology, Institute of Neurosciences, Universitat Autònoma de Barcelona, 01893 Bellaterra, Spain.
Sandra YesteWelab Barcelona, Parc Científic Barcelona, 08028 Barcelona, Spain.
Raquel F ReinosoWelab Barcelona, Parc Científic Barcelona, 08028 Barcelona, Spain.
Javier BurgueñoWelab Barcelona, Parc Científic Barcelona, 08028 Barcelona, Spain.
Ana MonteroWelab Barcelona, Parc Científic Barcelona, 08028 Barcelona, Spain.
Manuel MerlosWelab Barcelona, Parc Científic Barcelona, 08028 Barcelona, Spain.
José M VelaWelab Barcelona, Parc Científic Barcelona, 08028 Barcelona, Spain.
Mireia Herrando-GrabulosaDepartment of Cell Biology, Physiology and Immunology, Institute of Neurosciences, Universitat Autònoma de Barcelona, 01893 Bellaterra, Spain.
Xavier NavarroDepartment of Cell Biology, Physiology and Immunology, Institute of Neurosciences, Universitat Autònoma de Barcelona, 01893 Bellaterra, Spain.ORCID 0000-0001-9849-902X
Universitat Autònoma de Barcelona · ES

Funding

CIBERNED CB06/05/1105Ministerio de Ciencia, Innovación y Universidades of Spain RTI2018-096386-B-I00predoctoral fellowship of AGAUR, Departament d'Empresa i Coneixement de la Generalitat de Catalunya, cofounded by European Social Funds. FI-DGR 2017
6 · The paper itself

Abstract

Motor neuron diseases (MNDs) include sporadic and hereditary neurological disorders characterized by progressive degeneration of motor neurons (MNs). Sigma-1 receptor (Sig-1R) is a protein enriched in MNs, and mutations on its gene lead to various types of MND. Previous studies have suggested that Sig-1R is a target to prevent MN degeneration. In this study, two novel synthesized Sig-1R ligands, coded EST79232 and EST79376, from the same chemical series, with the same scaffold and similar physicochemical properties but opposite functionality on Sig-1R, were evaluated as neuroprotective compounds to prevent MN degeneration. We used an in vitro model of spinal cord organotypic cultures under chronic excitotoxicity and two in vivo models, the spinal nerve injury and the superoxide dismutase 1 (SOD1)

Indexed as

Amyotrophic Lateral SclerosisAnimalsDisease Models, AnimalLigandsMiceMice, TransgenicMotor NeuronsNeuroprotectionReceptors, sigmaSigma-1 ReceptorSpinal CordSuperoxide DismutaseSuperoxide Dismutase-1LigandsReceptors, sigmaSigma-1 ReceptorSuperoxide DismutaseSuperoxide Dismutase-1amyotrophic lateral sclerosismotoneuron degenerationsigma-1 receptorSOD1G93A micespinal nerve injury

Identifiers

PMID35743175
PMCPMC9223397
OpenAlexW4283020860

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.