Evidence map›Paper›PMID 39704560›Full record

ArticleThe Journal of physiology2025

Corticolimbic structures activation during preparation and execution of respiratory manoeuvres in voluntary olfactory sampling: An intracranial EEG study.

Jules Granget, Marie Cécile Niérat, Katia Lehongre, Virginie Lambrecq, Valerio Frazzini, Vincent Navarro, Nathalie Buonviso, Thomas Similowski

Abstract read
In one paragraph

Article in The Journal of physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Jules GrangetSorbonne Université, INSERM, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Paris, France.ORCID 0000-0001-8169-3854
Marie Cécile NiératSorbonne Université, INSERM, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Paris, France.
Katia LehongreParis Brain Institute, ICM, INSERM, CNRS, Sorbonne Université, Paris, France.
Virginie LambrecqParis Brain Institute, ICM, INSERM, CNRS, Sorbonne Université, Paris, France.
Valerio FrazziniParis Brain Institute, ICM, INSERM, CNRS, Sorbonne Université, Paris, France.
Vincent NavarroParis Brain Institute, ICM, INSERM, CNRS, Sorbonne Université, Paris, France.
Nathalie BuonvisoUniversité Lyon 1, CNRS UMR5292 INSERM U1028, Codage Mémoire Olfaction, Centre de Recherche en Neurosciences de Lyon, Lyon, France.ORCID 0000-0002-0018-1695
Thomas SimilowskiSorbonne Université, INSERM, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Paris, France.ORCID 0000-0003-2868-9279

Funding

Agence Nationale de la Recherche (ANR) ANR-22-CE37-0014Institut Universitaire d'Ingéniérie en Santé, Sorbonne Université, Paris, France doctoral fellowship
6 · The paper itself

Abstract

Volitional respiratory manoeuvres such as sniffing and apnoea play a key role in the active olfactory exploration of the environment. Their impairment by neurodegenerative processes could thus impair olfactory abilities with the ensuing impact on quality of life. Functional brain imaging studies have identified brain networks engaged in sniffing and voluntary apnoea, comprising the primary motor and somatosensory cortices, the insula, the anterior cingulate cortex and the amygdala. The temporal organization and the oscillatory activities of these networks are not known. To elucidate these aspects, we recorded intracranial electroencephalograms in six patients during voluntary sniffs and short apnoeas (12 s). The preparation phase of both manoeuvres involved increased alpha and theta activity in the posterior insula, amygdala and temporal regions, with a specific preparatory activity in the parahippocampus for the short apnoeas and the hippocampus for sniff. Subsequently, it narrowed to the superior and median temporal areas, immediately after the manoeuvres. During short apnoeas, a particular dynamic was observed, consisting of a rapid decline in alpha and theta activity followed by a slow recovery and increase. Volitional respiratory manoeuvres involved in olfactory control involve corticolimbic structures in both a preparatory and executive manner. Further studies are needed to determine whether diseases altering deep brain structures can disrupt these mechanisms and if such disruption contributes to the corresponding olfactory deficits. KEY POINTS: Both sniff manoeuvres and short apnoeas are associated with oscillatory activity predominantly in low-frequency bands (alpha and theta). Preparation of sniff manoeuvres and short apnoeas involve activities in low-frequency bands in the posterior insula and temporal regions that extend to amygdala during the execution of both manoeuvres. During short apnoeas, activities in low-frequency bands initially decline before continuously increasing until the apnoeas end.

Indexed as

Cerebral CortexSmellAdultAgedElectroencephalographyFemaleHumansMaleMiddle Agedapnoeabreathingcorticolimbic structuresintracerebral electroencephalogramolfactionrespiratory‐related brain networkssniffing

Identifiers

PMID39704560
PMCPMC11826067

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.