Evidence map›Paper›PMID 42679017›Full record

ArticlePloS one2026

Central and peripheral plasticity after chemical unilateral labyrinthectomy: Glial responses, calyces dynamics, and behavioral consequences.

Jessica Trico, Isabelle Watabe, Vinay Parameshwarappa, Agnes Lapotre, Louis Godaert, Alain Tonetto, Christian Chabbert, Andreas Zwergal, Brahim Tighilet

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jessica TricoAix Marseille Univ, CNRS, CRPN (Centre de Recherche en Psychologie et Neurosciences UMR 7077), Marseille, France.ORCID 0000-0002-1300-9499
Isabelle WatabeAix Marseille Univ, CNRS, CRPN (Centre de Recherche en Psychologie et Neurosciences UMR 7077), Marseille, France.ORCID 0000-0003-4881-8592
Vinay ParameshwarappaAix Marseille Univ, CNRS, CRPN (Centre de Recherche en Psychologie et Neurosciences UMR 7077), Marseille, France.
Agnes LapotreAix Marseille Univ, CNRS, CRPN (Centre de Recherche en Psychologie et Neurosciences UMR 7077), Marseille, France.
Louis GodaertAix Marseille Univ, CNRS, Centrale Med, FSCM (UAR1739), Plateforme de Recherche Analytique Technologique et Imagerie (PRATIM), Marseille, France.
Alain TonettoAix Marseille Univ, CNRS, Centrale Med, FSCM (UAR1739), Plateforme de Recherche Analytique Technologique et Imagerie (PRATIM), Marseille, France.
Christian ChabbertAix Marseille Univ, CNRS, CRPN (Centre de Recherche en Psychologie et Neurosciences UMR 7077), Marseille, France.
Andreas ZwergalDepartment of Neurology, LMU University Hospital, LMU Medizin, LMU Munich, Munich, Germany.
Brahim TighiletAix Marseille Univ, CNRS, CRPN (Centre de Recherche en Psychologie et Neurosciences UMR 7077), Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral vestibular disorders are highly prevalent, but the underlying neurobiological mechanisms remain poorly understood, particularly regarding bilateral peripheral plasticity following unilateral injury. Using a rat model of chemical unilateral labyrinthectomy (cUL) (SHAM, n = 14; cUL, n = 20), we combined behavioral analyses, auditory assessments, immunohistochemistry, and histological quantification to characterize central and peripheral adaptations from 1 to 30 days after vestibular deafferentation. cUL induced significant postural deficits from day 1, while hyperactivity and anxiety-like behaviors emerged from day 9 and persisted over time. In the deafferented medial vestibular nucleus, robust glial reactivity developed rapidly (day 3) whereas only astrocytes remained significantly elevated throughout the observation period. Histological analyses revealed a marked loss of type I hair cell calyces in the ipsilateral utricle to ototoxic exposure at both acute (D3) and chronic (D30) time points. Unexpectedly, the contralateral utricle also exhibited a transient reduction in calyceal endings at D3 (p < 0.01), which recovered by D30, revealing previously unrecognized bilateral peripheral vestibular plasticity following unilateral vestibular injury. In contrast, cochlear alterations remained restricted to the ipsilateral side of ototoxic exposure indicating distinct adaptive responses in the auditory and vestibular organs. Together, these findings demonstrate that unilateral vestibular injury triggers coordinated central glial reactivity and contralateral peripheral vestibular plasticity, providing new insight into the cellular mechanisms underlying vestibular compensation.

Indexed as

Behavior, AnimalNeurogliaNeuronal PlasticityVestibule, LabyrinthAnimalsMaleRatsRats, Sprague-Dawley

Identifiers

PMID42679017
PMCPMC13533426

What Socratic holds

Textmetadata
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 Socratic graph.