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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
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