Intestinal distension orchestrates neuronal activity in the enteric nervous system of adult mice

Author:

Cavin Jean‐Baptiste1234,Wongkrasant Preedajit1234,Glover Joel B.15,Balemba Onesmo B.6ORCID,MacNaughton Wallace K.134ORCID,Sharkey Keith A.124ORCID

Affiliation:

1. Snyder Institute for Chronic Diseases University of Calgary Calgary Alberta Canada

2. Hotchkiss Brain Institute University of Calgary Calgary Alberta Canada

3. Inflammation Research Network University of Calgary Calgary Alberta Canada

4. Department of Physiology and Pharmacology University of Calgary Calgary Alberta Canada

5. Live Cell Imaging Laboratory, Cumming School of Medicine University of Calgary Calgary Alberta Canada

6. Department of Biological Sciences University of Idaho Moscow ID USA

Abstract

AbstractThe enteric nervous system (ENS) regulates the motor, secretory and defensive functions of the gastrointestinal tract. Enteric neurons integrate mechanical and chemical inputs from the gut lumen to generate complex motor outputs. How intact enteric neural circuits respond to changes in the gut lumen is not well understood. We recorded intracellular calcium in live‐cell confocal recordings in neurons from intact segments of mouse intestine in order to investigate neuronal response to luminal mechanical and chemical stimuli. Wnt1‐, ChAT‐ and Calb1‐GCaMP6 mice were used to record neurons from the jejunum and colon. We measured neuronal calcium response to KCl (75 mM), veratridine (10 μM), 1,1‐dimethyl‐4‐phenylpiperazinium (DMPP; 100 μM) or luminal nutrients (Ensure®), in the presence or absence of intraluminal distension. In the jejunum and colon, distension generated by the presence of luminal content (chyme and faecal pellets, respectively) renders the underlying enteric circuit unresponsive to depolarizing stimuli. In the distal colon, high levels of distension inhibit neuronal response to KCl, while intermediate levels of distension reorganize Ca2+ response in circumferentially propagating slow waves. Mechanosensitive channel inhibition suppresses distension‐induced Ca2+ elevations, and calcium‐activated potassium channel inhibition restores neuronal response to KCl, but not DMPP in the distended colon. In the jejunum, distension prevents a previously unknown tetrodotoxin‐resistant neuronal response to luminal nutrient stimulation. Our results demonstrate that intestinal distension regulates the excitability of ENS circuits via mechanosensitive channels. Physiological levels of distension locally silence or synchronize neurons, dynamically regulating the excitability of enteric neural circuits based on the content of the intestinal lumen. imageKey points How the enteric nervous system of the gastrointestinal tract responds to luminal distension remains to be fully elucidated. Here it is shown that intestinal distension modifies intracellular calcium levels in the underlying enteric neuronal network, locally and reversibly silencing neurons in the distended regions. In the distal colon, luminal distension is integrated by specific mechanosensitive channels and coordinates the dynamics of neuronal activation within the enteric network. In the jejunum, distension suppresses the neuronal calcium responses induced by luminal nutrients. Physiological levels of distension dynamically regulate the excitability of enteric neuronal circuits.

Funder

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

Human Frontier Science Program

Publisher

Wiley

Subject

Physiology

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Tetrodotoxin‐resistant mechanosensitivity and L‐type calcium channel‐mediated spontaneous calcium activity in enteric neurons;Experimental Physiology;2024-07-09

2. The recruitment of mechanosensitive enteric neurons in the guinea pig gastric fundus is dependent on ganglionic stretch level;Neurogastroenterology & Motility;2024-06-30

3. Neuroimmunophysiology of the gastrointestinal tract;American Journal of Physiology-Gastrointestinal and Liver Physiology;2024-06-01

4. Calcium image analysis in the moving gut;Neurogastroenterology & Motility;2023-09-22

5. Piezo1 in Digestive System Function and Dysfunction;International Journal of Molecular Sciences;2023-08-19

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