Volumetric mapping of the functional neuroanatomy of the respiratory network in the perfused brainstem preparation of rats.

brainstem functional neuroanatomy local field potential respiratory phase transition respiratory rhythm generation synchronization

Journal

The Journal of physiology
ISSN: 1469-7793
Titre abrégé: J Physiol
Pays: England
ID NLM: 0266262

Informations de publication

Date de publication:
06 2020
Historique:
received: 23 01 2020
accepted: 05 02 2020
pubmed: 27 2 2020
medline: 16 2 2021
entrez: 27 2 2020
Statut: ppublish

Résumé

The functional neuroanatomy of the mammalian respiratory network is far from being understood since experimental tools that measure neural activity across this brainstem-wide circuit are lacking. Here, we use silicon multi-electrode arrays to record respiratory local field potentials (rLFPs) from 196-364 electrode sites within 8-10 mm While it is widely accepted that inspiratory rhythm generation depends on the pre-Bötzinger complex, the functional neuroanatomy of the neural circuits that generate expiration is debated. We hypothesized that the compartmental organization of the brainstem respiratory network is sufficient to generate macroscopic local field potentials (LFPs), and if so, respiratory (r) LFPs could be used to map the functional neuroanatomy of the respiratory network. We developed an approach using silicon multi-electrode arrays to record spontaneous LFPs from hundreds of electrode sites in a volume of brainstem tissue while monitoring the respiratory motor pattern on phrenic and vagal nerves in the perfused brainstem preparation. Our results revealed the expression of rLFPs across the pontomedullary brainstem. rLFPs occurred specifically at the three transitions between respiratory phases: (1) from late expiration (E2) to inspiration (I), (2) from I to post-inspiration (PI), and (3) from PI to E2. Thus, respiratory network activity was maximal at respiratory phase transitions. Spatially, the E2-I, and PI-E2 transitions were anatomically localized to the ventral and dorsal respiratory groups, respectively. In contrast, our data show, for the first time, that the generation of controlled expiration during the post-inspiratory phase engages a distributed neuronal population within ventral, dorsal and pontine network compartments. A group-wise independent component analysis demonstrated that all preparations exhibited rLFPs with a similar temporal structure and thus share a similar functional neuroanatomy. Thus, volumetric mapping of rLFPs could allow for the physiological assessment of global respiratory network organization in health and disease.

Identifiants

pubmed: 32100293
doi: 10.1113/JP279605
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2061-2079

Subventions

Organisme : NIH HHS
ID : NIBIB EB021960
Pays : United States
Organisme : NIH HHS
ID : NIBIB EB021960
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 The Authors. The Journal of Physiology © 2020 The Physiological Society.

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Auteurs

Rishi R Dhingra (RR)

The Florey Institute of Neuroscience & Mental Health, University of Melbourne, Melbourne, Australia.

Thomas E Dick (TE)

Division of Pulmonary, Critical Care & Sleep, Department of Medicine, Case Western Reserve University, Cleveland, USA.

Werner I Furuya (WI)

The Florey Institute of Neuroscience & Mental Health, University of Melbourne, Melbourne, Australia.

Roberto F Galán (RF)

Department of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, USA.

Mathias Dutschmann (M)

The Florey Institute of Neuroscience & Mental Health, University of Melbourne, Melbourne, Australia.

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