Evidence map›Paper›PMID 33250858›Full record

ReviewFrontiers in endocrinology2020

Cytoprotective and Neurotrophic Effects of Octadecaneuropeptide (ODN) in

Olfa Masmoudi-Kouki, Amira Namsi, Yosra Hamdi, Seyma Bahdoudi, Ikram Ghouili, Julien Chuquet, Jérôme Leprince, Benjamin Lefranc, Taoufik Ghrairi, Marie-Christine Tonon and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

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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

12 authors at 6 institutions in 2 countries.

Olfa Masmoudi-KoukiLaboratory of Neurophysiology Cellular Physiopathology and Biomolecule Valorisation, LR18ES03, Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Amira NamsiLaboratory of Neurophysiology Cellular Physiopathology and Biomolecule Valorisation, LR18ES03, Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Yosra HamdiLaboratory of Neurophysiology Cellular Physiopathology and Biomolecule Valorisation, LR18ES03, Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Seyma BahdoudiLaboratory of Neurophysiology Cellular Physiopathology and Biomolecule Valorisation, LR18ES03, Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Ikram GhouiliLaboratory of Neurophysiology Cellular Physiopathology and Biomolecule Valorisation, LR18ES03, Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Julien ChuquetNormandy University, Neuronal and Neuroendocrine Differentiation and Communication, Inserm U1239, Rouen, France.
Jérôme LeprinceNormandy University, Neuronal and Neuroendocrine Differentiation and Communication, Inserm U1239, Rouen, France.
Benjamin LefrancNormandy University, Neuronal and Neuroendocrine Differentiation and Communication, Inserm U1239, Rouen, France.
Taoufik GhrairiLaboratory of Neurophysiology Cellular Physiopathology and Biomolecule Valorisation, LR18ES03, Faculty of Sciences of Tunis, University Tunis El Manar, Tunis, Tunisia.
Marie-Christine TononNormandy University, Neuronal and Neuroendocrine Differentiation and Communication, Inserm U1239, Rouen, France.
Gérard LizardTeam Bio-PeroxIL, Biochemistry of the Peroxisome, Inflammation and Lipid Metabolism/University Bourgogne Franche-Comté (UBFC)/Inserm, Dijon, France.
David VaudryNormandy University, Neuronal and Neuroendocrine Differentiation and Communication, Inserm U1239, Rouen, France.
Inserm · FRTunis University · TNDifférenciation et Communication Neuronale et Neuroendocrine · FRTunis El Manar University · TNInstitute for Research and Innovation in Biomedicine · FRUniversité de Bourgogne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Octadecaneuropeptide (ODN) and its precursor diazepam-binding inhibitor (DBI) are peptides belonging to the family of endozepines. Endozepines are exclusively produced by astroglial cells in the central nervous system of mammals, and their release is regulated by stress signals and neuroactive compounds. There is now compelling evidence that the gliopeptide ODN protects cultured neurons and astrocytes from apoptotic cell death induced by various neurotoxic agents.

Indexed as

Disease Models, AnimalAnimalsCytoprotectionDiazepam Binding InhibitorHumansMiceNerve Growth FactorsNeurodegenerative DiseasesNeuropeptidesNeuroprotectionNeuroprotective AgentsOxidative StressPeptide FragmentsDiazepam Binding Inhibitordiazepam binding inhibitor (33-50)Nerve Growth FactorsNeuropeptidesNeuroprotective AgentsPeptide Fragmentscell differentiationcell protectiongliopeptide ODNneurodegenerationoxidative stress

Identifiers

PMID33250858
PMCPMC7672186
OpenAlexW3094975747

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.