Effects of optogenetic activation of the enteric nervous system on gastrointestinal motility in mouse small intestine.


Journal

Autonomic neuroscience : basic & clinical
ISSN: 1872-7484
Titre abrégé: Auton Neurosci
Pays: Netherlands
ID NLM: 100909359

Informations de publication

Date de publication:
12 2020
Historique:
received: 05 04 2020
revised: 17 08 2020
accepted: 16 09 2020
pubmed: 28 9 2020
medline: 6 10 2021
entrez: 27 9 2020
Statut: ppublish

Résumé

Recently, it was demonstrated that optogenetics could be used to stimulate enteric calretinin neurons, leading to increased colonic transit in vitro and in vivo. The aim of the current study was to determine if similar approaches could be used to stimulate the isolated mouse small intestine, with the aim of potentially also improving transit in the small bowel. Cre-Lox recombination was used to generate transgenic mice expressing the light-sensitive ion channel channelrhodopsin-2 (ChR2) in calretinin neurons. Spontaneous migrating motor complexes were recorded from isolated terminal small intestine in both Cal Focal illumination of the small intestine does not appear as effective at inducing propulsive motor activity as has been demonstrated in the colon of the same colony mice. This study suggests caution should be exercised when assuming optogenetic technology is equally effective at increasing GI transit in the small intestine as in the large intestine of mice.

Sections du résumé

BACKGROUND AND AIMS
Recently, it was demonstrated that optogenetics could be used to stimulate enteric calretinin neurons, leading to increased colonic transit in vitro and in vivo. The aim of the current study was to determine if similar approaches could be used to stimulate the isolated mouse small intestine, with the aim of potentially also improving transit in the small bowel.
METHODS
Cre-Lox recombination was used to generate transgenic mice expressing the light-sensitive ion channel channelrhodopsin-2 (ChR2) in calretinin neurons.
RESULTS
Spontaneous migrating motor complexes were recorded from isolated terminal small intestine in both Cal
CONCLUSION
Focal illumination of the small intestine does not appear as effective at inducing propulsive motor activity as has been demonstrated in the colon of the same colony mice. This study suggests caution should be exercised when assuming optogenetic technology is equally effective at increasing GI transit in the small intestine as in the large intestine of mice.

Identifiants

pubmed: 32980660
pii: S1566-0702(20)30167-3
doi: 10.1016/j.autneu.2020.102733
pmc: PMC9884517
mid: NIHMS1864619
pii:
doi:

Substances chimiques

Calb2 protein, mouse 0
Calbindin 2 0
Channelrhodopsins 0

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

102733

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK052574
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK103901
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM101218
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Références

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pubmed: 14754993
Cell Tissue Res. 2008 Nov;334(2):147-61
pubmed: 18855018
Gastroenterology. 2017 May;152(6):1407-1418
pubmed: 28115057
Cell Tissue Res. 1996 Apr;284(1):39-53
pubmed: 8601295
Neurogastroenterol Motil. 2002 Dec;14(6):657-65
pubmed: 12464088
J Physiol. 2003 Dec 15;553(Pt 3):881-93
pubmed: 14514874
Expert Rev Gastroenterol Hepatol. 2019 Apr;13(4):281-284
pubmed: 30791770
Gastroenterology. 2018 Aug;155(2):514-528.e6
pubmed: 29782847

Auteurs

Nick J Spencer (NJ)

Visceral Neurophysiology Laboratory, College of Medicine and Public Health, Centre for Neuroscience, Flinders University, Bedford Park, South Australia 5042, Australia. Electronic address: nicholas.spencer@flinders.edu.au.

Lee Travis (L)

Visceral Neurophysiology Laboratory, College of Medicine and Public Health, Centre for Neuroscience, Flinders University, Bedford Park, South Australia 5042, Australia.

Tim Hibberd (T)

Visceral Neurophysiology Laboratory, College of Medicine and Public Health, Centre for Neuroscience, Flinders University, Bedford Park, South Australia 5042, Australia.

Nigel Kelly (N)

SA Biomedical Engineering, SA Health, Government of South Australia, Australia.

Jing Feng (J)

Department of Anesthesiology, The Center for the Study of Itch, Washington University, St Louis, MO, USA.

Hongzhen Hu (H)

Department of Anesthesiology, The Center for the Study of Itch, Washington University, St Louis, MO, USA. Electronic address: hongzhen.hu@wustl.edu.

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Classifications MeSH