Evidence map›Paper›PMID 29700421›Full record

ArticleScientific reports2018

Ultra-slow mechanical stimulation of olfactory epithelium modulates consciousness by slowing cerebral rhythms in humans.

A Piarulli, A Zaccaro, M Laurino, D Menicucci, A De Vito, L Bruschini, S Berrettini, M Bergamasco, S Laureys, A Gemignani

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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  17. Functional Connectivity of the Chemosenses: A Review.Frontiers in systems neuroscience · 2022
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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

10 authors at 5 institutions in 2 countries.

A PiarulliDepartment of Surgical, Medical, Molecular and Critical Area Pathology, University of Pisa, Via Roma 65, 56126, Pisa, Italy.
A ZaccaroDepartment of Surgical, Medical, Molecular and Critical Area Pathology, University of Pisa, Via Roma 65, 56126, Pisa, Italy.
M LaurinoInstitute of Clinical Physiology, National Research Council (CNR), Via Giuseppe Moruzzi 1, 56127, Pisa, Italy.
D MenicucciDepartment of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Via Risorgimento 36, 56126, Pisa, Italy.
A De VitoAzienda Ospedaliero-Universitaria Pisana (University Hospital, AOUP), Via Paradisa 2, 56124, Pisa, Italy.
L BruschiniDepartment of Surgical, Medical, Molecular and Critical Area Pathology, University of Pisa, Via Roma 65, 56126, Pisa, Italy.
S BerrettiniDepartment of Surgical, Medical, Molecular and Critical Area Pathology, University of Pisa, Via Roma 65, 56126, Pisa, Italy.
M BergamascoPERCRO Laboratory, TECIP Institute, Sant'Anna School of Advanced Studies, Via Alamanni 13B, 56010, Ghezzano, Pisa, Italy.
S LaureysComa Science Group, GIGA Research Center, University and University Hospital of Liège, Avenue de l'Hôpital 11, 4000, Liège, Belgium.
A GemignaniDepartment of Surgical, Medical, Molecular and Critical Area Pathology, University of Pisa, Via Roma 65, 56126, Pisa, Italy. angelo.gemignani@unipi.it.
University of Pisa · ITIstituto di Fisiologia Clinica · ITUniversity of Liège · BEAzienda Ospedaliera Universitaria Pisana · ITScuola Superiore Sant'Anna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The coupling between respiration and neural activity within olfactory areas and hippocampus has recently been unambiguously demonstrated, its neurophysiological basis sustained by the well-assessed mechanical sensitivity of the olfactory epithelium. We herein hypothesize that this coupling reverberates to the whole brain, possibly modulating the subject's behavior and state of consciousness. The olfactory epithelium of 12 healthy subjects was stimulated with periodical odorless air-delivery (frequency 0.05 Hz, 8 s on, 12 off). Cortical electrical activity (High Density-EEG) and perceived state of consciousness have been studied. The stimulation induced i) an enhancement of delta-theta EEG activity over the whole cortex mainly involving the Limbic System and Default Mode Network structures, ii) a reversal of the overall information flow directionality from wake-like postero-anterior to NREM sleep-like antero-posterior, iii) the perception of having experienced an Altered State of Consciousness. These findings could shed further light via a neurophenomenological approach on the links between respiration, cerebral activity and subjective experience, suggesting a plausible neurophysiological basis for interpreting altered states of consciousness induced by respiration-based meditative practices.

Indexed as

Brain WavesConsciousnessPhysical StimulationBrain MappingCerebral CortexElectroencephalographyHumansOlfactory MucosaPsychometrics

Identifiers

PMID29700421
PMCPMC5919905
OpenAlexW2803747688

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.