Nocturnal swallowing augments arousal intensity and arousal tachycardia.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
14 04 2020
Historique:
pubmed: 2 4 2020
medline: 22 7 2020
entrez: 2 4 2020
Statut: ppublish

Résumé

Cortical arousal from sleep is associated with autonomic activation and acute increases in heart rate. Arousals vary considerably in their frequency, intensity/duration, and physiological effects. Sleep and arousability impact health acutely (daytime cognitive function) and long-term (cardiovascular outcomes). Yet factors that modify the arousal intensity and autonomic activity remain enigmatic. In this study of healthy human adults, we examined whether reflex airway defense mechanisms, specifically swallowing or glottic adduction, influenced cardiac autonomic activity and cortical arousal from sleep. We found, in all subjects, that swallows trigger rapid, robust, and patterned tachycardia conserved across wake, sleep, and arousal states. Tachycardia onset was temporally matched to glottic adduction-the first phase of swallow motor program. Multiple swallows increase the magnitude of tachycardia via temporal summation, and blood pressure increases as a function of the degree of tachycardia. During sleep, swallows were overwhelmingly associated with arousal. Critically, swallows were causally linked to the intense, prolonged cortical arousals and marked tachycardia. Arousal duration and tachycardia increased in parallel as a function of swallow incidence. Our findings suggest that cortical feedback and tachycardia are integrated responses of the swallow motor program. Our work highlights the functional influence of episodic, involuntary airway defense reflexes on sleep and vigilance and cardiovascular function in healthy individuals.

Identifiants

pubmed: 32229567
pii: 1907393117
doi: 10.1073/pnas.1907393117
pmc: PMC7165485
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8624-8632

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

P G R Burke (PGR)

Neuroscience Research Australia, Randwick, NSW 2031, Australia; p.burke@neura.edu.au.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.
Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, NSW 2109, Australia.

S G Carter (SG)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

F Knapman (F)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

J Patti (J)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

M Butlin (M)

Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, NSW 2109, Australia.

S C Gandevia (SC)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

J E Butler (JE)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

D J Eckert (DJ)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.
Adelaide Institute for Sleep Health, Flinders University, Bedford Park, SA 5042, Australia.

L E Bilston (LE)

Neuroscience Research Australia, Randwick, NSW 2031, Australia.
Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

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