Evidence map›Paper›PMID 27927961›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Nasal Respiration Entrains Human Limbic Oscillations and Modulates Cognitive Function.

Christina Zelano, Heidi Jiang, Guangyu Zhou, Nikita Arora, Stephan Schuele, Joshua Rosenow, Jay A Gottfried

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 300 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
300citing papers in PubMed, 3 pooled it
19.0field-weighted citation impact, top 1% 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.

NCT05846425 naunknown statusnot on this mapstarted 2023, after this paper: background citation

Investigating the Effect of Yoga-based Breathing Styles on the Human Brain, With a Focus on Memory

TypeinterventionalSponsorUniversität des SaarlandesRan2023 to 2024Enrolled75ConditionsHypoventilation, HyperventilationArmsNose-breathing training, Mouth-breathing training
NCT07505914 narecruitingnot on this mapstarted 2026, after this paper: background citation

Comparing Different Breathing Exercises Added to Balance Training on Cognitive and Functional Outcomes in Elderly Population

TypeinterventionalSponsorIstanbul University - CerrahpasaRan2026 to 2026Enrolled40ConditionsOlder Adults (65 Years and Older), Cognition, Balance Control in Elderly, Fall Prevention in Healthy AgingArmsBalance Training Program, Inspiratory Muscle Training, Breathing Exercise Program
3 · Its place in the literature

Who cites it

300 citing papers in PubMed, 3 syntheses or guidelines pooled it, 608 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Article
  11. Article
  12. Article
  13. Article
  14. A nose-to-brain circuit underlies anxiety regulation by nasal afferent frequency in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Synchrony and Reciprocity in Rhythmic Interaction.Annals of the New York Academy of Sciences · 2026
    Review

240 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Christina ZelanoDepartments of Neurology and c-zelano@northwestern.edu.
Heidi JiangDepartments of Neurology and.
Guangyu ZhouDepartments of Neurology and.ORCID 0000-0003-0897-6465
Nikita AroraDepartments of Neurology and.ORCID 0000-0002-6311-4588
Stephan SchueleDepartments of Neurology and.ORCID 0000-0003-3261-7120
Joshua RosenowNeurosurgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, and.
Jay A GottfriedDepartments of Neurology and.
Northwestern University · USNorthwestern Medicine · US

Funding

The function of respiratory-linked local field potential oscillations in human olfactory and limbic brain regionsR01DC016364 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZELANO, CHRISTINA MARIA · 2018 to 2022
$2.1M
Spatiotemporal Mechanisms of Olfactory Processing in the Human BrainR01DC013243 · NIDCD · UNIVERSITY OF PENNSYLVANIA · PI GOTTFRIED, JAY A · 2013 to 2017
$1.5M
Attention-dependent neural oscillations in the human olfactory systemR00DC012803 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ZELANO, CHRISTINA MARIA · 2015 to 2017
$732k
Spatiotemporal Coding in the Human Olfactory SystemR21DC012014 · NIDCD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI GOTTFRIED, JAY A · 2011 to 2012
$419k
NIDCD NIH HHS R00 DC012803NIDCD NIH HHS R01 DC013243NIDCD NIH HHS R01 DC016364NIDCD NIH HHS R21 DC012014
6 · The paper itself

Abstract

The need to breathe links the mammalian olfactory system inextricably to the respiratory rhythms that draw air through the nose. In rodents and other small animals, slow oscillations of local field potential activity are driven at the rate of breathing (∼2-12 Hz) in olfactory bulb and cortex, and faster oscillatory bursts are coupled to specific phases of the respiratory cycle. These dynamic rhythms are thought to regulate cortical excitability and coordinate network interactions, helping to shape olfactory coding, memory, and behavior. However, while respiratory oscillations are a ubiquitous hallmark of olfactory system function in animals, direct evidence for such patterns is lacking in humans. In this study, we acquired intracranial EEG data from rare patients (Ps) with medically refractory epilepsy, enabling us to test the hypothesis that cortical oscillatory activity would be entrained to the human respiratory cycle, albeit at the much slower rhythm of ∼0.16-0.33 Hz. Our results reveal that natural breathing synchronizes electrical activity in human piriform (olfactory) cortex, as well as in limbic-related brain areas, including amygdala and hippocampus. Notably, oscillatory power peaked during inspiration and dissipated when breathing was diverted from nose to mouth. Parallel behavioral experiments showed that breathing phase enhances fear discrimination and memory retrieval. Our findings provide a unique framework for understanding the pivotal role of nasal breathing in coordinating neuronal oscillations to support stimulus processing and behavior. SIGNIFICANCE STATEMENT: Animal studies have long shown that olfactory oscillatory activity emerges in line with the natural rhythm of breathing, even in the absence of an odor stimulus. Whether the breathing cycle induces cortical oscillations in the human brain is poorly understood. In this study, we collected intracranial EEG data from rare patients with medically intractable epilepsy, and found evidence for respiratory entrainment of local field potential activity in human piriform cortex, amygdala, and hippocampus. These effects diminished when breathing was diverted to the mouth, highlighting the importance of nasal airflow for generating respiratory oscillations. Finally, behavioral data in healthy subjects suggest that breathing phase systematically influences cognitive tasks related to amygdala and hippocampal functions.

Indexed as

AdultAmygdalaChildCognitionDiscrimination, PsychologicalElectroencephalographyEpilepsyFearFemaleHippocampusHumansLimbic SystemMaleMental RecallMiddle AgedNasal Cavityamygdalahippocampuslocal field potentialpiriform cortexrespirationrespiratory oscillations

Identifiers

PMID27927961
PMCPMC5148230
OpenAlexW2560663849

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.