Cited by 74Neuroscience of respiration and sleepRespiratory and Cough-Related ResearchRespiratory Support and Mechanisms

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Anatomy and physiology of phrenic afferent neurons

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Abstract

Large-diameter myelinated phrenic afferents discharge in phase with diaphragm contraction, and smaller diameter fibers discharge across the respiratory cycle. In this article, we review the phrenic afferent literature and highlight areas in need of further study. We conclude that 1 ) activation of both myelinated and nonmyelinated phrenic sensory afferents can influence respiratory motor output on a breath-by-breath basis; 2 ) the relative impact of phrenic afferents substantially increases with diaphragm work and fatigue; 3 ) activation of phrenic afferents has a powerful impact on sympathetic motor outflow, and 4 ) phrenic afferents contribute to diaphragm somatosensation and the conscious perception of breathing. Much remains to be learned regarding the spinal and supraspinal distribution and synaptic contacts of myelinated and nonmyelinated phrenic afferents. Similarly, very little is known regarding the potential role of phrenic afferent neurons in triggering or modulating expression of respiratory neuroplasticity.

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  • Respiratory-related activity is observed in the somatosensory cortex, both in humans and in different parts of the rodent or cat somatosensory cortex: the whisker barrel cortex, trunk and nose representation.

    “First, respiratory-related activity is observed in the somatosensory cortex, both in humans 137,140 and in different parts of the rodent or cat somatosensory cortex: the whisker barrel cortex 118,141 , trunk 122,123 and nose 142 representation.”

    From Interoceptive rhythms in the brain (2023) · cites this paper as [123]

  • Diaphragm stretch and contraction are relayed by the phrenic nerve up to primary somatosensory cortex.

    “Diaphragm stretch and contraction are relayed by the phrenic nerve up to primary somatosensory cortex 122,123 ,”

    From Interoceptive rhythms in the brain (2023) · cites this paper as [123]

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Metadata

Authors
Nair, J., Streeter, K. A., Turner, S. M. F., Sunshine, M. D., Bolser, D. C., Fox, E. J., Davenport, P. W., & Fuller, D. D.
Affiliations
  • University of Florida Health (US)
  • University of Florida (US)
Corresponding author
Fuller, David D.
Venue
Journal of Neurophysiology
Published
2017-12-01
Volume
118
Issue
6
Pages
2975-2990
ISSN
  • 0022-3077 (ISSN-L)
  • 1522-1598
OpenAlex
W2746764939
Cited by
74
References
1
Citations by year
2026: 12 · 2025: 8 · 2024: 11 · 2023: 7 · 2022: 13 · 2021: 8 · 2020: 6 · 2019: 6 · 2018: 2 · 2017: 1
FWCI
0.50
Type
journal article
Language
en
Open access
Locations
  • Journal of Neurophysiology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • NIH (1OT2OD001983-01, 1R01NS080180-01A1, 1F32NS095620-01, T32-ND043730)
  • Craig H. Neilsen Foundation
  • State of Florida
Topics
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroscience of respiration and sleep
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory and Cough-Related Research
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Respiratory Support and Mechanisms
Keywords
phrenic nerve, diaphragm, respiratory motor control, diaphragm fatigue, respiratory neuroplasticity, synaptic connectivity, spinal cord
MeSH terms
Animals, Diaphragm, Humans, Neuronal Plasticity, Neurons, Afferent, Phrenic Nerve, Respiration, Nociception

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