On the presence and functional significance of sympathetic premotor neurons with collateralized spinal axons in the rat.


Journal

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

Informations de publication

Date de publication:
07 2019
Historique:
received: 22 01 2019
accepted: 23 04 2019
pubmed: 12 5 2019
medline: 28 7 2020
entrez: 12 5 2019
Statut: ppublish

Résumé

Spinally-projecting neurons of the rostral ventrolateral medulla (RVLM) determine sympathetic outflow to different territories of the body. Previous studies suggest the existence of RVLM neurons with distinct functional classes, such as neurons that target sympathetic nerves bound for functionally-similar tissue types (e.g. muscle vasculature). The existence of RVLM neurons with more general actions had not been critically tested. Using viral tracing, we show that a significant minority of RVLM neurons send axon collaterals to disparate spinal segments (T We investigate the extent of spinal axon collateralization of rat rostral ventrolateral medulla (RVLM) sympathetic premotor neurons and its functional consequences. In anatomical tracing experiments, two recombinant herpes viral vectors with retrograde tropism and expressing different fluorophores were injected into the intermediolateral column at upper thoracic and lower thoracic levels. Histological analysis revealed that ∼21% of RVLM bulbospinal neurons were retrogradely labelled by both vectors, indicating substantial axonal collateralization to disparate spinal segments. In functional experiments, another virus with retrograde tropism, a canine adenovirus expressing Cre recombinase, was injected into the left intermediolateral horn around the thoracolumbar junction, whereas a Cre-dependent viral vector encoding Channelrhodopsin2 under LoxP control was injected into the ipsilateral RVLM. In subsequent terminal experiments, blue laser light (473 nm × 20 ms pulses at 10 mW) was used to activate RVLM neurons that had been transduced by both vectors. Stimulus-locked activation, at appropriate latencies, was recorded in the following pairs of sympathetic nerves: forelimb and hindlimb muscle sympathetic fibres, as well as cardiac and either hindlimb muscle or lumbar sympathetic nerves. The latter result demonstrates that axon collaterals of lumbar-projecting RVLM neurons project to, and excite, both functionally similar (forelimb and hindlimb muscle) and functionally dissimilar (lumbar and cardiac) preganglionic neurons. Taken together, these findings show that the axons of a significant proportion of RVLM neurons collateralise widely within the spinal cord, and that they may excite preganglionic neurons of more than one functional class.

Identifiants

pubmed: 31077360
doi: 10.1113/JP277661
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3407-3423

Subventions

Organisme : British Heart Foundation
ID : RG/12/6/29670
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 088373
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 The Authors. The Journal of Physiology © 2019 The Physiological Society.

Auteurs

David G S Farmer (DGS)

Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, VIC, Australia.

Natasha Pracejus (N)

Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, VIC, Australia.

Bowen Dempsey (B)

Neuroscience Paris-Saclay Institute (Neuro-PSI), CNRS, Gif-Sur-Yvette, France.

Anita Turner (A)

Faculty of Medicine & Health Science, Macquarie University, North Ryde, NSW, Australia.

Phillip Bokiniec (P)

Department of Neuroscience, Max Delbrück Center for Molecular Medicine (MDC), Berlin-Buch, Germany, Neuroscience Research Center and Cluster of Excellence NeuroCure, Charité-Universitätsmedizin, Berlin, Germany.

Julian F R Paton (JFR)

Department of Physiology, Faculty of Medical & Health Sciences, University of Auckland, Park Road, Grafton, Auckland, New Zealand.

Anthony E Pickering (AE)

School of Physiology, Pharmacology & Neuroscience, Biomedical Sciences, University of Bristol, Bristol, UK.

Jasmine Burguet (J)

Institut Jean-Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris-Saclay, Versailles, France.

Philippe Andrey (P)

Institut Jean-Pierre Bourgin, INRA, AgroParisTech, CNRS, Université Paris-Saclay, Versailles, France.

Ann K Goodchild (AK)

Faculty of Medicine & Health Science, Macquarie University, North Ryde, NSW, Australia.

Robin M McAllen (RM)

Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, VIC, Australia.

Simon McMullan (S)

Faculty of Medicine & Health Science, Macquarie University, North Ryde, NSW, Australia.

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Classifications MeSH