Evidence map›Paper›PMID 31905931›Full record

ReviewInternational journal of molecular sciences2019

Role of c-Jun N-Terminal Kinases (JNKs) in Epilepsy and Metabolic Cognitive Impairment.

Oriol Busquets, Miren Ettcheto, Amanda Cano, Patricia R Manzine, Elena Sánchez-Lopez, Triana Espinosa-Jiménez, Ester Verdaguer, Rubén Dario Castro-Torres, Carlos Beas-Zarate, Francesc X Sureda and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 27 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

14 authors at 5 institutions in 4 countries.

Oriol BusquetsDepartment of Pharmacology, Toxicology and Therapeutic Chemistry, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain.
Miren EttchetoDepartment of Pharmacology, Toxicology and Therapeutic Chemistry, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain.
Amanda CanoBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Patricia R ManzineDepartment of Gerontology, Federal University of São Carlos (UFSCar), São Carlos 13565-905, Brazil.
Elena Sánchez-LopezInstitute of Nanoscience and Nanotechnology (IN2UB), University of Barcelona, 08028 Barcelona, Spain.ORCID 0000-0003-2571-108X
Triana Espinosa-JiménezDepartment of Pharmacology, Toxicology and Therapeutic Chemistry, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain.
Ester VerdaguerBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Rubén Dario Castro-TorresDepartment of Pharmacology, Toxicology and Therapeutic Chemistry, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain.
Carlos Beas-ZarateDepartment of Cellular and Molecular Biology, C.U.C.B.A., University of Guadalajara and Neuroscience Division, Sierra Mojada, Col. Independencia, Zapopan, Guadalajara, Jalisco 45200, Mexico.
Francesc X SuredaDepartment of Biochemistry and Biotechnology, Faculty of Medicine and Life Science, University Rovira i Virgili, 43201 Reus, Spain.ORCID 0000-0002-7968-3929
Jordi OlloquequiLaboratory of Cellular and Molecular Pathology, Instituto de Ciencias Biomédicas, Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Talca 3460000, Chile.
Carme AuladellBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Jaume FolchDepartment of Biochemistry and Biotechnology, Faculty of Medicine and Life Science, University Rovira i Virgili, 43201 Reus, Spain.
Antoni CaminsDepartment of Pharmacology, Toxicology and Therapeutic Chemistry, Faculty of Pharmacy and Food Science, University of Barcelona, 08028 Barcelona, Spain.ORCID 0000-0002-1229-5956
Instituto de Salud Carlos III · ESUniversidad de Guadalajara · MXInstitut de Nanociència i Nanotecnologia de la Universitat de BarcelonaUniversidad Autónoma de Chile · CLUniversidade Federal de São Carlos · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies have reported that the regulatory function of the different c-Jun N-terminal kinases isoforms (JNK1, JNK2, and JNK3) play an essential role in neurological disorders, such as epilepsy and metabolic-cognitive alterations. Accordingly, JNKs have emerged as suitable therapeutic strategies. In fact, it has been demonstrated that some unspecific JNK inhibitors exert antidiabetic and neuroprotective effects, albeit they usually show high toxicity or lack therapeutic value. In this sense, natural specific JNK inhibitors, such as Licochalcone A, are promising candidates. Nonetheless, research on the understanding of the role of each of the JNKs remains mandatory in order to progress on the identification of new selective JNK isoform inhibitors. In the present review, a summary on the current gathered data on the role of JNKs in pathology is presented, as well as a discussion on their potential role in pathologies like epilepsy and metabolic-cognitive injury. Moreover, data on the effects of synthetic small molecule inhibitors that modulate JNK-dependent pathways in the brain and peripheral tissues is reviewed.

Indexed as

AnimalsBrainCognitive DysfunctionDiabetes Mellitus, Type 2Endoplasmic Reticulum StressEpilepsyHumansHypoglycemic AgentsJNK Mitogen-Activated Protein KinasesMAP Kinase Signaling SystemMitochondriaMitogen-Activated Protein KinasesNeuroprotective AgentsProtein IsoformsHypoglycemic AgentsJNK Mitogen-Activated Protein KinasesMitogen-Activated Protein KinasesNeuroprotective AgentsProtein Isoformsbrainc-Jun-N-terminal kinasecognitive impairmentepilepsyJNK inhibitormetabolismtype 2 diabetes

Identifiers

PMID31905931
PMCPMC6981493
OpenAlexW2997197397

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.