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Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch
BACKGROUND: Intestinal sensitivity to mechanical stimuli has been studied intensively in visceral pain studies. The ability to sense different stimuli in the gut and translate these to physiological outcomes relies on the mechanosensory and transductive capacity of intrinsic intestinal nerves. Howev...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582074/ https://www.ncbi.nlm.nih.gov/pubmed/33123188 http://dx.doi.org/10.1155/2020/8834651 |
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author | Liao, Donghua Zhao, Jingbo Gregersen, Hans |
author_facet | Liao, Donghua Zhao, Jingbo Gregersen, Hans |
author_sort | Liao, Donghua |
collection | PubMed |
description | BACKGROUND: Intestinal sensitivity to mechanical stimuli has been studied intensively in visceral pain studies. The ability to sense different stimuli in the gut and translate these to physiological outcomes relies on the mechanosensory and transductive capacity of intrinsic intestinal nerves. However, the nature of the mechanosensitive channels and principal mechanical stimulus for mechanosensitive receptors are unknown. To be able to characterize intestinal mechanoelectrical transduction, that is, the molecular basis of mechanosensation, comprehensive mathematical models to predict responses of the sensory neurons to controlled mechanical stimuli are needed. This study aims to develop a biophysically based mathematical model of the myenteric neuron with the parameters constrained by learning from existing experimental data. Findings. The conductance-based single-compartment model was selected. The parameters in the model were optimized by using a combination of hand tuning and automated estimation. Using the optimized parameters, the model successfully predicted the electrophysiological features of the myenteric neurons with and without mechanical stimulation. CONCLUSIONS: The model provides a method to predict features and levels of detail of the underlying physiological system in generating myenteric neuron responses. The model could be used as building blocks in future large-scale network simulations of intrinsic primary afferent neurons and their network. |
format | Online Article Text |
id | pubmed-7582074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-75820742020-10-28 Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch Liao, Donghua Zhao, Jingbo Gregersen, Hans Comput Intell Neurosci Research Article BACKGROUND: Intestinal sensitivity to mechanical stimuli has been studied intensively in visceral pain studies. The ability to sense different stimuli in the gut and translate these to physiological outcomes relies on the mechanosensory and transductive capacity of intrinsic intestinal nerves. However, the nature of the mechanosensitive channels and principal mechanical stimulus for mechanosensitive receptors are unknown. To be able to characterize intestinal mechanoelectrical transduction, that is, the molecular basis of mechanosensation, comprehensive mathematical models to predict responses of the sensory neurons to controlled mechanical stimuli are needed. This study aims to develop a biophysically based mathematical model of the myenteric neuron with the parameters constrained by learning from existing experimental data. Findings. The conductance-based single-compartment model was selected. The parameters in the model were optimized by using a combination of hand tuning and automated estimation. Using the optimized parameters, the model successfully predicted the electrophysiological features of the myenteric neurons with and without mechanical stimulation. CONCLUSIONS: The model provides a method to predict features and levels of detail of the underlying physiological system in generating myenteric neuron responses. The model could be used as building blocks in future large-scale network simulations of intrinsic primary afferent neurons and their network. Hindawi 2020-10-13 /pmc/articles/PMC7582074/ /pubmed/33123188 http://dx.doi.org/10.1155/2020/8834651 Text en Copyright © 2020 Donghua Liao et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Liao, Donghua Zhao, Jingbo Gregersen, Hans Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch |
title | Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch |
title_full | Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch |
title_fullStr | Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch |
title_full_unstemmed | Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch |
title_short | Simulations of Myenteric Neuron Dynamics in Response to Mechanical Stretch |
title_sort | simulations of myenteric neuron dynamics in response to mechanical stretch |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582074/ https://www.ncbi.nlm.nih.gov/pubmed/33123188 http://dx.doi.org/10.1155/2020/8834651 |
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