Motor patterns in the proximal and distal mouse colon which underlie formation and propulsion of feces.


Journal

Neurogastroenterology and motility
ISSN: 1365-2982
Titre abrégé: Neurogastroenterol Motil
Pays: England
ID NLM: 9432572

Informations de publication

Date de publication:
07 2021
Historique:
revised: 30 12 2020
received: 16 10 2020
accepted: 26 01 2021
pubmed: 16 2 2021
medline: 19 1 2022
entrez: 15 2 2021
Statut: ppublish

Résumé

In herbivores, the proximal and distal colonic regions feature distinct motor patterns underlying formation and propulsion of fecal pellets, respectively. Omnivores, such as mice and humans, lack a similar clear anatomical transition between colonic regions. We investigated whether distinct processes form and propel content along the large intestine of a mouse (an omnivore). We recorded propulsive and non-propulsive neurogenic motor activity in mouse large intestine under six different stimulus conditions of varying viscosities. Gut wall movements were recorded by video and smooth muscle electrical behavior recorded with extracellular suction electrodes. Three major neurally mediated motor patterns contributed to pellet formation and propulsion. (1) Pellet-shaped boluses are pinched off near the ceco-colonic junction and slowly propelled distally to a transition located at 40% length along the colon. (2) At this functional colonic flexure, propulsion speed is significantly increased by self-sustaining neural peristalsis. Speed transition at this location also occurs with artificial pellets and with spontaneously formed boluses in the empty colon. (3) Periodic colonic motor complexes (CMCs) were present in all conditions reaching a maximal frequency of about 0.4 cpm and extending across the proximal and distal colon with faster speed of propagation. The three motor patterns share a unique underlying fundamental property of the enteric circuits, which involve extended ensembles of enteric neurons firing at close to 2 Hz. The demonstration of distinct functional differences between proximal and distal colon in rabbit, guinea pig, and now mouse raises the possibility that this may be an organizational principle in other mammalian species, including humans.

Sections du résumé

BACKGROUND
In herbivores, the proximal and distal colonic regions feature distinct motor patterns underlying formation and propulsion of fecal pellets, respectively. Omnivores, such as mice and humans, lack a similar clear anatomical transition between colonic regions. We investigated whether distinct processes form and propel content along the large intestine of a mouse (an omnivore).
METHODS
We recorded propulsive and non-propulsive neurogenic motor activity in mouse large intestine under six different stimulus conditions of varying viscosities. Gut wall movements were recorded by video and smooth muscle electrical behavior recorded with extracellular suction electrodes.
KEY RESULTS
Three major neurally mediated motor patterns contributed to pellet formation and propulsion. (1) Pellet-shaped boluses are pinched off near the ceco-colonic junction and slowly propelled distally to a transition located at 40% length along the colon. (2) At this functional colonic flexure, propulsion speed is significantly increased by self-sustaining neural peristalsis. Speed transition at this location also occurs with artificial pellets and with spontaneously formed boluses in the empty colon. (3) Periodic colonic motor complexes (CMCs) were present in all conditions reaching a maximal frequency of about 0.4 cpm and extending across the proximal and distal colon with faster speed of propagation.
CONCLUSIONS AND INFERENCES
The three motor patterns share a unique underlying fundamental property of the enteric circuits, which involve extended ensembles of enteric neurons firing at close to 2 Hz. The demonstration of distinct functional differences between proximal and distal colon in rabbit, guinea pig, and now mouse raises the possibility that this may be an organizational principle in other mammalian species, including humans.

Identifiants

pubmed: 33586835
doi: 10.1111/nmo.14098
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14098

Informations de copyright

© 2021 John Wiley & Sons Ltd.

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Auteurs

Marcello Costa (M)

College of Medicine and Public Health, Discipline of Human Physiology Flinders University, Adelaide, SA, Australia.

Lauren J Keightley (LJ)

College of Medicine and Public Health, Discipline of Human Physiology Flinders University, Adelaide, SA, Australia.

Timothy J Hibberd (TJ)

College of Medicine and Public Health, Discipline of Human Physiology Flinders University, Adelaide, SA, Australia.

Lukasz Wiklendt (L)

Discipline of Surgery and Gastroenterology, Flinders Medical Centre, Adelaide, SA, Australia.

Phil G Dinning (PG)

Discipline of Surgery and Gastroenterology, Flinders Medical Centre, Adelaide, SA, Australia.

Simon J Brookes (SJ)

College of Medicine and Public Health, Discipline of Human Physiology Flinders University, Adelaide, SA, Australia.

Nick J Spencer (NJ)

College of Medicine and Public Health, Discipline of Human Physiology Flinders University, Adelaide, SA, Australia.

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