Evidence map›Paper›PMID 40275427›Full record

ArticleBiological research2025

Olfactory dysfunction and altered cortical excitability in the mouse model of Fragile X Syndrome.

Felipe Arancibia, Marcelo Rojas, Diego Becerra, Rocío Fuenzalida, Christian Cea-Del Rio, Jorge Mpodozis, Magdalena Sanhueza, Alexia Nunez-Parra

Abstract read
In one paragraph

Article in Biological research, 2025. 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
–field-weighted citation impact
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.

  1. Article
  2. Distinct Synaptic Mechanisms DrivebioRxiv : the preprint server for biology · 2025
    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.

Felipe ArancibiaCellular Physiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile.
Marcelo RojasCellular Physiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile.ORCID https://orcid.org/0009-0000-1139-9502
Diego BecerraCellular Physiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile.
Rocío FuenzalidaCellular Physiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile.
Christian Cea-Del RioNeurophysiopathology Laboratory, Center for Biomedical and Applied Research, School of Medicine, Faculty of Medical Sciences, Universidad de Santiago de Chile, Santiago, Chile.ORCID https://orcid.org/0000-0002-4658-2427
Jorge MpodozisNeurobiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile.
Magdalena SanhuezaCellular Physiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile.ORCID https://orcid.org/0000-0001-8073-0385
Alexia Nunez-ParraCellular Physiology Laboratory, Biology Department, Faculty of Science, Universidad de Chile, Santiago, Chile. alexianunez@uchile.cl.ORCID http://orcid.org/0000-0003-0239-2493

Funding

Fondecyt 11150897
6 · The paper itself

Abstract

Fragile X Syndrome (FXS) is the most common monogenetic cause of autism and inherited intellectual disability. A key feature of FXS symptomatology is altered sensory processing greatly affecting FXS individual's life quality. Here, we use a combination of behavioral tests and slice physiology tools to study the neurophysiological alterations underlying aberrant sensory processing in the olfactory system of the FXS mouse model (Fmr1 KO). We focused on the piriform cortex (PC), since it is in this brain region where olfactory information is integrated and ultimately decoded. Using a go-no go behavioral task we have found that Fmr1 KO learn to discriminate between a rewarded and a not rewarded odorant but cannot distinguish complex odor mixtures, akin to what is found in the environment. Moreover, Fmr1 KO long-term memory is impaired compared to control mice suggesting possibly cortical processing alterations. In addition, electrophysiological data from PC layer II neurons of Fmr1 KO mice showed a hyperexcitable phenotype manifested by differences in active membrane properties and altered network connectivity. Taken together, our data suggest a possible causal link between the observed olfactory discrimination deficiencies in the Fmr1 KO mouse and the altered physiology of PC.

Indexed as

Cortical ExcitabilityFragile X SyndromeOlfaction DisordersPiriform CortexAnimalsBehavior, AnimalDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1MaleMiceMice, Inbred C57BLMice, KnockoutFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Autism spectrum disorder (ASD)Fmr1 KOOlfactory discriminationPerceptual stabilitySensory processing

Identifiers

PMID40275427
PMCPMC12023451

What OpenQuestion holds

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LicenceCC BY
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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.