Cargando…
Development and characterization of a chronic implant mouse model for vagus nerve stimulation
Vagus nerve stimulation (VNS) suppresses inflammation and autoimmune diseases in preclinical and clinical studies. The underlying molecular, neurological, and anatomical mechanisms have been well characterized using acute electrophysiological stimulation of the vagus. However, there are several unan...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051950/ https://www.ncbi.nlm.nih.gov/pubmed/33821789 http://dx.doi.org/10.7554/eLife.61270 |
_version_ | 1783679835060568064 |
---|---|
author | Mughrabi, Ibrahim T Hickman, Jordan Jayaprakash, Naveen Thompson, Dane Ahmed, Umair Papadoyannis, Eleni S Chang, Yao-Chuan Abbas, Adam Datta-Chaudhuri, Timir Chang, Eric H Zanos, Theodoros P Lee, Sunhee C Froemke, Robert C Tracey, Kevin J Welle, Cristin Al-Abed, Yousef Zanos, Stavros |
author_facet | Mughrabi, Ibrahim T Hickman, Jordan Jayaprakash, Naveen Thompson, Dane Ahmed, Umair Papadoyannis, Eleni S Chang, Yao-Chuan Abbas, Adam Datta-Chaudhuri, Timir Chang, Eric H Zanos, Theodoros P Lee, Sunhee C Froemke, Robert C Tracey, Kevin J Welle, Cristin Al-Abed, Yousef Zanos, Stavros |
author_sort | Mughrabi, Ibrahim T |
collection | PubMed |
description | Vagus nerve stimulation (VNS) suppresses inflammation and autoimmune diseases in preclinical and clinical studies. The underlying molecular, neurological, and anatomical mechanisms have been well characterized using acute electrophysiological stimulation of the vagus. However, there are several unanswered mechanistic questions about the effects of chronic VNS, which require solving numerous technical challenges for a long-term interface with the vagus in mice. Here, we describe a scalable model for long-term VNS in mice developed and validated in four research laboratories. We observed significant heart rate responses for at least 4 weeks in 60–90% of animals. Device implantation did not impair vagus-mediated reflexes. VNS using this implant significantly suppressed TNF levels in endotoxemia. Histological examination of implanted nerves revealed fibrotic encapsulation without axonal pathology. This model may be useful to study the physiology of the vagus and provides a tool to systematically investigate long-term VNS as therapy for chronic diseases modeled in mice. |
format | Online Article Text |
id | pubmed-8051950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-80519502021-04-21 Development and characterization of a chronic implant mouse model for vagus nerve stimulation Mughrabi, Ibrahim T Hickman, Jordan Jayaprakash, Naveen Thompson, Dane Ahmed, Umair Papadoyannis, Eleni S Chang, Yao-Chuan Abbas, Adam Datta-Chaudhuri, Timir Chang, Eric H Zanos, Theodoros P Lee, Sunhee C Froemke, Robert C Tracey, Kevin J Welle, Cristin Al-Abed, Yousef Zanos, Stavros eLife Immunology and Inflammation Vagus nerve stimulation (VNS) suppresses inflammation and autoimmune diseases in preclinical and clinical studies. The underlying molecular, neurological, and anatomical mechanisms have been well characterized using acute electrophysiological stimulation of the vagus. However, there are several unanswered mechanistic questions about the effects of chronic VNS, which require solving numerous technical challenges for a long-term interface with the vagus in mice. Here, we describe a scalable model for long-term VNS in mice developed and validated in four research laboratories. We observed significant heart rate responses for at least 4 weeks in 60–90% of animals. Device implantation did not impair vagus-mediated reflexes. VNS using this implant significantly suppressed TNF levels in endotoxemia. Histological examination of implanted nerves revealed fibrotic encapsulation without axonal pathology. This model may be useful to study the physiology of the vagus and provides a tool to systematically investigate long-term VNS as therapy for chronic diseases modeled in mice. eLife Sciences Publications, Ltd 2021-04-06 /pmc/articles/PMC8051950/ /pubmed/33821789 http://dx.doi.org/10.7554/eLife.61270 Text en © 2021, Mughrabi et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology and Inflammation Mughrabi, Ibrahim T Hickman, Jordan Jayaprakash, Naveen Thompson, Dane Ahmed, Umair Papadoyannis, Eleni S Chang, Yao-Chuan Abbas, Adam Datta-Chaudhuri, Timir Chang, Eric H Zanos, Theodoros P Lee, Sunhee C Froemke, Robert C Tracey, Kevin J Welle, Cristin Al-Abed, Yousef Zanos, Stavros Development and characterization of a chronic implant mouse model for vagus nerve stimulation |
title | Development and characterization of a chronic implant mouse model for vagus nerve stimulation |
title_full | Development and characterization of a chronic implant mouse model for vagus nerve stimulation |
title_fullStr | Development and characterization of a chronic implant mouse model for vagus nerve stimulation |
title_full_unstemmed | Development and characterization of a chronic implant mouse model for vagus nerve stimulation |
title_short | Development and characterization of a chronic implant mouse model for vagus nerve stimulation |
title_sort | development and characterization of a chronic implant mouse model for vagus nerve stimulation |
topic | Immunology and Inflammation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8051950/ https://www.ncbi.nlm.nih.gov/pubmed/33821789 http://dx.doi.org/10.7554/eLife.61270 |
work_keys_str_mv | AT mughrabiibrahimt developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT hickmanjordan developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT jayaprakashnaveen developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT thompsondane developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT ahmedumair developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT papadoyanniselenis developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT changyaochuan developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT abbasadam developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT dattachaudhuritimir developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT changerich developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT zanostheodorosp developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT leesunheec developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT froemkerobertc developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT traceykevinj developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT wellecristin developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT alabedyousef developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation AT zanosstavros developmentandcharacterizationofachronicimplantmousemodelforvagusnervestimulation |