Evidence map›Paper›PMID 35188290›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2022

Lipid mediator n-3 docosapentaenoic acid-derived protectin D1 enhances synaptic inhibition of hippocampal principal neurons by interaction with a G-protein-coupled receptor.

Apostolos Mikroulis, Marco Ledri, Gabriele Ruffolo, Eleonora Palma, Günther Sperk, Jesmond Dalli, Annamaria Vezzani, Merab Kokaia

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

8 authors at 6 institutions in 4 countries.

Apostolos MikroulisEpilepsy Center, Department of Clinical Sciences, Faculty of Medicine, Lund University, Lund, Sweden.
Marco LedriEpilepsy Center, Department of Clinical Sciences, Faculty of Medicine, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0001-8317-7976
Gabriele RuffoloDepartment of Physiology and Pharmacology, Istituto Pasteur-Fondazione Cenci Bolognetti, University of Rome Sapienza, Rome, Italy.
Eleonora PalmaDepartment of Physiology and Pharmacology, Istituto Pasteur-Fondazione Cenci Bolognetti, University of Rome Sapienza, Rome, Italy.
Günther SperkDepartment of Pharmacology, Medical University Innsbruck, Innsbruck, Austria.
Jesmond DalliWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID https://orcid.org/0000-0001-6328-3640
Annamaria VezzaniMario Negri Institute for Pharmacological Research IRCCS, Milan, Italy.
Merab KokaiaEpilepsy Center, Department of Clinical Sciences, Faculty of Medicine, Lund University, Lund, Sweden.
Lund University · SEInnsbruck Medical University · ATIRCCS Ospedale San Raffaele · ITIstituto Pasteur · ITMario Negri Institute for Pharmacological Research · ITQueen Mary University of London · GB

Funding

Wellcome TrustWellcome Trust 107613/Z/15/Z
6 · The paper itself

Abstract

Epilepsy is a severe neurological disease manifested by spontaneous recurrent seizures due to abnormal hyper-synchronization of neuronal activity. Epilepsy affects about 1% of the population and up to 40% of patients experience seizures that are resistant to currently available drugs, thus highlighting an urgent need for novel treatments. In this regard, anti-inflammatory drugs emerged as potential therapeutic candidates. In particular, specific molecules apt to resolve the neuroinflammatory response occurring in acquired epilepsies have been proven to counteract seizures in experimental models, and humans. One candidate investigational molecule has been recently identified as the lipid mediator n-3 docosapentaenoic acid-derived protectin D1 (PD1

Indexed as

Inhibitory Postsynaptic PotentialsAnimalsCA1 Region, HippocampalDocosahexaenoic AcidsMiceMice, Inbred C57BLNeuronsReceptors, Cell SurfaceXenopusDocosahexaenoic Acidspertussis toxin receptorprotectin D1Receptors, Cell Surfaceantiepileptic mechanismGABAA receptorsmouse hippocampusPD1n-3DPAperisomatic inhibition

Identifiers

PMID35188290
PMCPMC9306510
OpenAlexW4213076584

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.