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Respiration

Anatomy and Physiology · NLM MeSH · updated 2026-10-31 · version 1

Citations verified against PubMedNot yet clinician-reviewed10 referencesApproximately 5 min read

The act of breathing with the lungs, consisting of inhalation, or the taking into the lungs of the ambient air, and of exhalation, or the expelling of the modified air which contains more carbon dioxide than the air taken in (Blak

Table of Contents

1. Definition2. Research landscape3. Reading the evidence4. Open-access studies5. Key reviews6. References7. About this article

Definition and research guide

This page combines a MeSH definition, publication statistics and selected research abstracts. It is a starting point for reading the literature, not a medical textbook or a systematic evidence review.

Content available: 4 complete abstracts (840 words), 10 references. Full article text is not stored or reproduced here; follow the PMID, DOI or PMC links to read the original sources and their access terms.

Definition

The act of breathing with the lungs, consisting of inhalation, or the taking into the lungs of the ambient air, and of exhalation, or the expelling of the modified air which contains more carbon dioxide than the air taken in (Blakiston's Gould Medical Dictionary, 4th ed.). This does not include tissue respiration (= oxygen consumption) or cell respiration (= cell respiration).

Definition: NLM Medical Subject Headings (MeSH) scope note (Public domain (U.S. National Library of Medicine); attribution requested). View the MeSH record.

Also known as: Breathing.

Where it fits in the MeSH classification

Broader topics
Respiratory Physiological Phenomena
Narrower topics
Breath Holding; Respiratory Mechanics; Respiratory Rate; Respiratory Transport
See also
Apnea; Breath Tests; Breathing Exercises; Dyspnea; Mouth Breathing; Oxygen Consumption; Cell Respiration

Related concepts

  • Lung
  • Inhalation
  • Exhalation
  • Carbon Dioxide
  • Oxygen Consumption
  • Cell Respiration

Research landscape

PubMed indexes 127,086 records tagged with the MeSH heading “Respiration” (counts retrieved 2026-10-31). 11,191 of them (8.8%) were published from 2020 onward, and the busiest period so far is through 1999 with 73,627 records.

Reviews account for 8,605 records (6.8%) and meta-analyses for 273. Randomized controlled trials number 6,150 (4.8%) as a share of all records on the topic.

PubMed records by publication periodthrough 1999: 73,627 records; 2000-2009: 19,638 records; 2010-2019: 22,630 records; 2020 onward: 11,191 records73,627through 199919,6382000-200922,6302010-201911,1912020 onward
Records in PubMed indexed with this heading, by publication period. Real counts from NCBI E-utilities; the final period covers only part of the current year. Volume reflects how much has been published, not how strong the evidence is.
Show the data
PeriodRecords
through 199973,627
2000-200919,638
2010-201922,630
2020 onward11,191
Share of records by publication typeReviews: 6.8 percent; Meta-analyses: 0.2 percent; Randomized controlled trials: 4.8 percentReviews6.8% (8,605)Meta-analyses0.2% (273)Randomized controlled trials4.8% (6,150)
Share of all PubMed records on this heading that carry each publication type. Types overlap with other records, so the shares do not sum to 100%.
Publication-type chart data
Publication types among 127,086 PubMed records
TypeRecordsShare
Reviews8,6056.8%
Meta-analyses2730.2%
Randomized controlled trials6,1504.8%

Method: PubMed query "Respiration"[MeSH Terms] with publication-type and date filters, retrieved 2026-10-31.

Reading the evidence in anatomy and physiology

Anatomy describes how body structures are built and physiology describes how they normally work, so most findings here are descriptive or mechanistic rather than evidence about treatment. Much of what is known comes from dissection, imaging, tissue studies and experiments in animals, and measurements in healthy volunteers can differ from those in people with disease or at different ages. Normal ranges vary between individuals and populations. Check whether a result was measured in people or in another species, the age and health of the participants, and the method used.

Evidence from open-access studies

These open-access studies come from PubMed’s best-match results for this heading (papers whose main topic it is), ranked here by citation count, with one recent addition. Each abstract is reproduced in full under its recorded open licence so that you can read the authors’ own words. They illustrate the literature; they are not a systematic summary of it. Citation counts measure attention, not reliability or clinical benefit.

Study comparison — selected abstracts, not a systematic review
Study / authorsYearSource label / designEurope PMC citationsLicence / source
Respiration Facilitates Behavior During Multisensory Integration
Saltafossi M, Zaccaro A, Kluger DS, Perrucci MG, Ferri F, Costantini M
2025Research article
Design not recorded in structured metadata
12cc by
PMID 40999648 · DOI · PMC12464358
Human cerebrospinal fluid net flow enhanced by respiration during the awake state
Lim S, Cogswell PM, Jacobson DN, Kandimalla M, Choi Y, Nycklemoe M, et al.
2025Research article
Design not recorded in structured metadata
6cc by
PMID 41390815 · DOI · PMC12749403
Pleasant odors specifically promote a soothing autonomic response and brain-body coupling through respiratory modulation
Ghibaudo V, Turrel M, Granget J, Souilhol M, Garcia S, Plailly J, et al.
2025Research article
Design not recorded in structured metadata
5cc by
PMID 41107329 · DOI · PMC12534574
Breath, Pulse, and Speech: A Multi-Parameter Wearable System using Airflow-Thermoelectric Fusion Technology
Zhu Z, Yan X, Hou Y, Zeng Y, Li Z, Sun X, et al.
2026Research article
Design not recorded in structured metadata
4cc by
PMID 41144845 · DOI · PMC12822444

Respiration Facilitates Behavior During Multisensory Integration [1]

Research article Saltafossi M, Zaccaro A, Kluger DS, Perrucci MG, Ferri F, Costantini M · · 2025 · cited 12 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
The brain processes information from the external environment alongside signals generated by the body.
Closing excerpt
This suggests that, rather than a mere bottom-up mechanism, respiration is actively adjusted to maximize the signal-to-noise balance between interoceptive and exteroceptive signals.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (189 words)

The brain processes information from the external environment alongside signals generated by the body. Among bodily rhythms, respiration emerges as a key modulator of sensory processing. Multisensory integration, the non-linear combination of information from multiple senses to reduce environmental uncertainty, may be influenced by respiratory dynamics. This study investigated how respiration modulates reaction times and multisensory integration in a simple detection task. Forty healthy participants were presented with unimodal (Auditory, Visual, Tactile) and bimodal (Audio-Tactile, Audio-Visual, Visuo-Tactile) stimuli while their respiratory activity was recorded. Results revealed that reaction times systematically varied with respiration, with faster responses during peak inspiration and early expiration but slower responses during the expiration-to-inspiration transition. Applying the race model inequality approach to quantify multisensory integration, we found that Audio-Tactile and Audio-Visual stimuli exhibited the highest integration during the expiration-to-inspiration phase. These findings conceivably reflect respiration phase-locked changes in cortical excitability which in turn orchestrates multisensory integration. Interestingly, participants also tended to adapt their respiratory cycles, aligning response onsets preferentially with early expiration. This suggests that, rather than a mere bottom-up mechanism, respiration is actively adjusted to maximize the signal-to-noise balance between interoceptive and exteroceptive signals.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 40999648 · DOI · PMC12464358

Human cerebrospinal fluid net flow enhanced by respiration during the awake state [2]

Research article Lim S, Cogswell PM, Jacobson DN, Kandimalla M, Choi Y, Nycklemoe M, et al. · · 2025 · cited 6 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Cerebrospinal fluid dynamics play a crucial role in maintaining brain homeostasis by delivering nutrients, transmitting immune signals, and clearing waste products.
Closing excerpt
Our findings identify respiration in the awake state as a modifiable, noninvasive mechanism that influences involuntary functions such as cerebrospinal fluid dynamics and may have implications for cerebrospinal fluid-mediated brain homeostasis.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (269 words)

Cerebrospinal fluid dynamics play a crucial role in maintaining brain homeostasis by delivering nutrients, transmitting immune signals, and clearing waste products. While cardiac activity primarily drives the pulsatile movement of cerebrospinal fluid, respiration has been shown to facilitate low-frequency oscillations and contribute to bulk flow. Recent studies suggest that enhancing respiratory function may be an effective intervention to modulate cerebrospinal fluid dynamics. This study included 20 individuals with long-term formal training in Seokmun Hoheup, a lower belly-centered breathing practice (mean ± SD age, 58.1 ± 17.3 years; 8 females), and 25 controls with no formal long-term breathing practice (mean ± SD age, 49.2 ± 20.2 years; 12 females). All underwent real-time velocity-encoding magnetic resonance imaging to assess cerebrospinal fluid movement at the foramen magnum and lateral ventricle during both regular breathing and deep breathing. Deep breathing enhances cerebrospinal fluid dynamics in both groups, increasing displacement and net flow, particularly at the foramen magnum. Seokmun Hoheup trained participants show greater cerebrospinal fluid movement than controls at both the foramen magnum and lateral ventricle. Even during regular breathing, trained participants show higher cerebrospinal fluid mean speed, displacement, and net flow. Among respiratory factors, inhale length and diaphragm displacement show the strongest correlations with cerebrospinal fluid movement. Respiration modulated cerebrospinal fluid dynamics through both mechanical enhancement of venous outflow and autonomic modulation of the heart, with mechanical effects predominating in the lateral ventricle and both pathways contributing to the foramen magnum. Our findings identify respiration in the awake state as a modifiable, noninvasive mechanism that influences involuntary functions such as cerebrospinal fluid dynamics and may have implications for cerebrospinal fluid-mediated brain homeostasis.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41390815 · DOI · PMC12749403

Pleasant odors specifically promote a soothing autonomic response and brain-body coupling through respiratory modulation [3]

Research article Ghibaudo V, Turrel M, Granget J, Souilhol M, Garcia S, Plailly J, et al. · · 2025 · cited 5 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
Neuronal oscillations are tightly linked to physiological rhythms, yet little is known about how sensory stimuli influence their coupling.
Closing excerpt
Our study highlights the potential of olfactory stimulation as a non-invasive tool for modulating brain rhythms and autonomic function.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (205 words)

Neuronal oscillations are tightly linked to physiological rhythms, yet little is known about how sensory stimuli influence their coupling. Here, we investigated whether pleasant odors and pleasant music modulate the coupling between respiration, autonomic activity, and brain oscillations. Using a within-subject design, we exposed participants to a personally pleasant odor and a personally pleasant music while recording respiratory and cardiac activity, feeling of relaxation, and respiration-locked EEG responses. Our results reveal that only odors induced a significant coupling between physiological and neural rhythms. Pleasant odors decreased respiratory rate, increased inspiratory volume, reduced heart rate, and enhanced heart rate variability (HRV). EEG analyses showed that this odor-induced respiratory slowing enhanced respiration-related brain activity in a temporo-parieto-central network, which is not observed with music. In contrast, music, regardless of tempo, increased subjective arousal without affecting autonomic or neural coupling. These findings suggest that pleasant odors engage an olfactomotor response, where an emotionally driven change in breathing rhythm enhances respiration-related neural oscillations. This mechanism may facilitate brain states associated with an increased feeling of relaxation and interoception, distinguishing odors as a unique sensory modality capable of promoting brain-body coupling. Our study highlights the potential of olfactory stimulation as a non-invasive tool for modulating brain rhythms and autonomic function.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41107329 · DOI · PMC12534574

Breath, Pulse, and Speech: A Multi-Parameter Wearable System using Airflow-Thermoelectric Fusion Technology [4]

Research article Zhu Z, Yan X, Hou Y, Zeng Y, Li Z, Sun X, et al. · · 2026 · cited 4 times (Europe PMC)

Abstract reading summary — source excerpts
Opening excerpt
In medical emergency scenarios, conventional single-parameter monitoring cannot fully assess patient conditions, and current technologies lack intelligent emergency-state recognition, which delays timely treatment.
Closing excerpt
These advances supplement the theoretical understanding of thermoelectric responses to physiological activities while providing decision support for emergency conditions, demonstrating considerable potential for clinical application.
Interpretation limits
Verbatim excerpts from the authors’ abstract; the closing excerpt may describe a finding, limitation or recommendation. Design, population, effect size and uncertainty have not been independently extracted or appraised. Read the complete abstract and linked paper before interpreting the findings.
Read complete abstract (177 words)

In medical emergency scenarios, conventional single-parameter monitoring cannot fully assess patient conditions, and current technologies lack intelligent emergency-state recognition, which delays timely treatment. To overcome these challenges, this study develops a high-performance flexible thermoelectric textile-based wearable system that generates a 139.7 mV open-circuit voltage at ΔT = 30 K. To prevent skin-thermoelectric contact from distorting sensor readings, a Kirigami spacer is integrated to ensure proper air gaps while maintaining flexibility and breathability. By integrating optical cardiac sensing, the system establishes a thermoelectric-optical system for wireless real-time cooperative monitoring of both respiration and cardiac activity. The research systematically investigates the effects of airflow velocity on thermoelectric output, leading to the development of an innovative dynamic airflow-thermoelectric response theory. This theory enables speech recognition through airflow variations with 98% accuracy. Additionally, the study creates a multi-source fusion recognition model that combines respiratory patterns, speech-airflow, and cardiac signals to identify emergency states with 98% accuracy. These advances supplement the theoretical understanding of thermoelectric responses to physiological activities while providing decision support for emergency conditions, demonstrating considerable potential for clinical application.

Abstract reproduced from the open-access article under the recorded cc by licence; © the authors. PMID 41144845 · DOI · PMC12822444

Key reviews and meta-analyses

The most cited review-type papers among PubMed’s best-match results for this heading, listed with bibliographic details only. Follow the links for the full text and access terms.

  • Research article ERS statement on respiratory muscle testing at rest and during exercise [5]
    Laveneziana P, Albuquerque A, Aliverti A, Babb T, Barreiro E, Dres M, et al. · Eur Respir J · 2019 · cited 567 times (Europe PMC)
  • Research article Piezos thrive under pressure: mechanically activated ion channels in health and disease [6]
    Murthy SE, Dubin AE, Patapoutian A · Nat Rev Mol Cell Biol · 2017 · cited 484 times (Europe PMC)
  • Research article Tuberculosis and lung damage: from epidemiology to pathophysiology [7]
    Ravimohan S, Kornfeld H, Weissman D, Bisson GP · Eur Respir Rev · 2018 · cited 365 times (Europe PMC)
  • Research article Prone position in ARDS patients: why, when, how and for whom [8]
    Guérin C, Albert RK, Beitler J, Gattinoni L, Jaber S, Marini JJ, et al. · Intensive Care Med · 2020 · cited 324 times (Europe PMC)
  • Research article Mechanical Ventilation: State of the Art [9]
    Pham T, Brochard LJ, Slutsky AS · Mayo Clin Proc · 2017 · cited 190 times (Europe PMC)
  • Research article Patient self-inflicted lung injury: implications for acute hypoxemic respiratory failure and ARDS patients on non-invasive support [10]
    Grieco DL, Menga LS, Eleuteri D, Antonelli M · Minerva Anestesiol · 2019 · cited 174 times (Europe PMC)

References

  1. Saltafossi M, Zaccaro A, Kluger DS, Perrucci MG, Ferri F, Costantini M. Respiration Facilitates Behavior During Multisensory Integration. . 2025. PMID 40999648 · DOI · PMC12464358
  2. Lim S, Cogswell PM, Jacobson DN, Kandimalla M, Choi Y, Nycklemoe M, et al.. Human cerebrospinal fluid net flow enhanced by respiration during the awake state. . 2025. PMID 41390815 · DOI · PMC12749403
  3. Ghibaudo V, Turrel M, Granget J, Souilhol M, Garcia S, Plailly J, et al.. Pleasant odors specifically promote a soothing autonomic response and brain-body coupling through respiratory modulation. . 2025. PMID 41107329 · DOI · PMC12534574
  4. Zhu Z, Yan X, Hou Y, Zeng Y, Li Z, Sun X, et al.. Breath, Pulse, and Speech: A Multi-Parameter Wearable System using Airflow-Thermoelectric Fusion Technology. . 2026. PMID 41144845 · DOI · PMC12822444
  5. Laveneziana P, Albuquerque A, Aliverti A, Babb T, Barreiro E, Dres M, et al.. ERS statement on respiratory muscle testing at rest and during exercise. Eur Respir J. 2019. PMID 30956204 · DOI
  6. Murthy SE, Dubin AE, Patapoutian A. Piezos thrive under pressure: mechanically activated ion channels in health and disease. Nat Rev Mol Cell Biol. 2017. PMID 28974772 · DOI
  7. Ravimohan S, Kornfeld H, Weissman D, Bisson GP. Tuberculosis and lung damage: from epidemiology to pathophysiology. Eur Respir Rev. 2018. PMID 29491034 · DOI · PMC6019552
  8. Guérin C, Albert RK, Beitler J, Gattinoni L, Jaber S, Marini JJ, et al.. Prone position in ARDS patients: why, when, how and for whom. Intensive Care Med. 2020. PMID 33169218 · DOI · PMC7652705
  9. Pham T, Brochard LJ, Slutsky AS. Mechanical Ventilation: State of the Art. Mayo Clin Proc. 2017. PMID 28870355 · DOI
  10. Grieco DL, Menga LS, Eleuteri D, Antonelli M. Patient self-inflicted lung injury: implications for acute hypoxemic respiratory failure and ARDS patients on non-invasive support. Minerva Anestesiol. 2019. PMID 30871304 · DOI

About this article

Sources
NLM Medical Subject Headings (definition, synonyms); NCBI PubMed (counts, identifiers); Europe PMC (open-access abstracts and citation counts).
Verification
Every reference was resolved against PubMed on 2026-10-31; title, year and DOI matched.
Review state
automated source verified; no human expert review has been recorded yet.
Version
1, last updated 2026-10-31.

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All 542 articles in Anatomy and Physiology →

At a glance

127,086
PubMed records on this heading
9%
published since 2020
8,605
review articles
6,150
randomized trials
10
verified references below

Counts come from PubMed on 2026-10-31; they show how much has been written, not how strong the evidence is.

Related topics See all →

  • Pulmonary Gas ExchangeAnatomy and Physiology
  • Respiratory MechanicsAnatomy and Physiology
  • Respiratory RateAnatomy and Physiology
  • BronchoconstrictionAnatomy and Physiology
  • Work of BreathingAnatomy and Physiology

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