Evidence map›Paper›PMID 36710925›Full record

ArticleFrontiers in molecular neuroscience2022

Regionally restricted modulation of

Annalisa Adinolfi, Gabriele Di Sante, Luca Rivignani Vaccari, Maria Tredicine, Francesco Ria, Davide Bonvissuto, Valentina Corvino, Claudio Sette, Maria Concetta Geloso

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Role of Sam68 in different types of cancer (Review).International journal of molecular medicine · 2025
    Review
  3. A novelFrontiers in cellular neuroscience · 2024
    Article
  4. New Challenges for Anatomists in the Era of Omics.Diagnostics (Basel, Switzerland) · 2023
    Review
  5. 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

9 authors at 2 institutions in 1 country.

Annalisa AdinolfiSection of Human Anatomy, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Gabriele Di SanteSection of Human, Clinic and Forensic Anatomy, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
Luca Rivignani VaccariSection of Human Anatomy, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Maria TredicineSection of General Pathology, Department of Translational Medicine and Surgery, Università Cattolica del Sacro Cuore, Rome, Italy.
Francesco RiaSection of General Pathology, Department of Translational Medicine and Surgery, Università Cattolica del Sacro Cuore, Rome, Italy.
Davide BonvissutoSection of Human Anatomy, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Valentina CorvinoSection of Human Anatomy, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Claudio SetteSection of Human Anatomy, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Maria Concetta GelosoSection of Human Anatomy, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Università Cattolica del Sacro Cuore · ITUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) and its preclinical models are characterized by marked changes in neuroplasticity, including excitatory/inhibitory imbalance and synaptic dysfunction that are believed to underlie the progressive cognitive impairment (CI), which represents a significant clinical hallmark of the disease. In this study, we investigated several parameters of neuroplasticity in the hippocampus of the experimental autoimmune encephalomyelitis (EAE) SJL/J mouse model, characterized by rostral inflammatory and demyelinating lesions similar to Relapsing-Remitting MS. By combining morphological and molecular analyses, we found that the hippocampus undergoes extensive inflammation in EAE-mice, more pronounced in the CA3 and dentate gyrus (DG) subfields than in the CA1, associated with changes in GABAergic circuitry, as indicated by the increased expression of the interneuron marker Parvalbumin selectively in CA3. By laser-microdissection, we investigated the impact of EAE on the alternative splicing of

Indexed as

alternative splicingArhgef9experimental autoimmune encephalomyelitishippocampusmultiple sclerosisneuroinflammationparvalbuminSam68

Identifiers

PMID36710925
PMCPMC9878567
OpenAlexW4315784268

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.