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Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model
Vagus nerve stimulation is emerging as a promising treatment for type 2 diabetes. Here, we evaluated the ability of stimulation of the vagus nerve to reduce glycemia in awake, freely moving metabolically compromised rats. A model of type 2 diabetes (n = 10) was induced using a high‐fat diet and low...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017977/ https://www.ncbi.nlm.nih.gov/pubmed/35439355 http://dx.doi.org/10.14814/phy2.15257 |
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author | Payne, Sophie C. Ward, Glenn Fallon, James B. Hyakumura, Tomoko Prins, Johannes B. Andrikopoulos, Sofianos MacIsaac, Richard J. Villalobos, Joel |
author_facet | Payne, Sophie C. Ward, Glenn Fallon, James B. Hyakumura, Tomoko Prins, Johannes B. Andrikopoulos, Sofianos MacIsaac, Richard J. Villalobos, Joel |
author_sort | Payne, Sophie C. |
collection | PubMed |
description | Vagus nerve stimulation is emerging as a promising treatment for type 2 diabetes. Here, we evaluated the ability of stimulation of the vagus nerve to reduce glycemia in awake, freely moving metabolically compromised rats. A model of type 2 diabetes (n = 10) was induced using a high‐fat diet and low doses of streptozotocin. Stimulation of the abdominal vagus nerve was achieved by pairing 15 Hz pulses on a distal pair of electrodes with high‐frequency blocking stimulation (26 kHz, 4 mA) on a proximal pair of electrodes to preferentially produce efferent conducting activity (eVNS). Stimulation was well tolerated in awake, freely moving rats. During 1 h of eVNS, glycemia decreased in 90% of subjects (−1.25 ± 1.25 mM h, p = 0.017), and 2 dB above neural threshold was established as the most effective “dose” of eVNS (p = 0.009). Following 5 weeks of implantation, eVNS was still effective, resulting in significantly decreased glycemia (−1.7 ± 0.6 mM h, p = 0.003) during 1 h of eVNS. There were no overt changes in fascicle area or signs of histopathological damage observed in implanted vagal nerve tissue following chronic implantation and stimulation. Demonstration of the biocompatibility and safety of eVNS in awake, metabolically compromised animals is a critical first step to establishing this therapy for clinical use. With further development, eVNS could be a promising novel therapy for treating type 2 diabetes. |
format | Online Article Text |
id | pubmed-9017977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90179772022-04-21 Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model Payne, Sophie C. Ward, Glenn Fallon, James B. Hyakumura, Tomoko Prins, Johannes B. Andrikopoulos, Sofianos MacIsaac, Richard J. Villalobos, Joel Physiol Rep Original Articles Vagus nerve stimulation is emerging as a promising treatment for type 2 diabetes. Here, we evaluated the ability of stimulation of the vagus nerve to reduce glycemia in awake, freely moving metabolically compromised rats. A model of type 2 diabetes (n = 10) was induced using a high‐fat diet and low doses of streptozotocin. Stimulation of the abdominal vagus nerve was achieved by pairing 15 Hz pulses on a distal pair of electrodes with high‐frequency blocking stimulation (26 kHz, 4 mA) on a proximal pair of electrodes to preferentially produce efferent conducting activity (eVNS). Stimulation was well tolerated in awake, freely moving rats. During 1 h of eVNS, glycemia decreased in 90% of subjects (−1.25 ± 1.25 mM h, p = 0.017), and 2 dB above neural threshold was established as the most effective “dose” of eVNS (p = 0.009). Following 5 weeks of implantation, eVNS was still effective, resulting in significantly decreased glycemia (−1.7 ± 0.6 mM h, p = 0.003) during 1 h of eVNS. There were no overt changes in fascicle area or signs of histopathological damage observed in implanted vagal nerve tissue following chronic implantation and stimulation. Demonstration of the biocompatibility and safety of eVNS in awake, metabolically compromised animals is a critical first step to establishing this therapy for clinical use. With further development, eVNS could be a promising novel therapy for treating type 2 diabetes. John Wiley and Sons Inc. 2022-04-19 /pmc/articles/PMC9017977/ /pubmed/35439355 http://dx.doi.org/10.14814/phy2.15257 Text en © 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Payne, Sophie C. Ward, Glenn Fallon, James B. Hyakumura, Tomoko Prins, Johannes B. Andrikopoulos, Sofianos MacIsaac, Richard J. Villalobos, Joel Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
title | Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
title_full | Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
title_fullStr | Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
title_full_unstemmed | Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
title_short | Blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
title_sort | blood glucose modulation and safety of efferent vagus nerve stimulation in a type 2 diabetic rat model |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017977/ https://www.ncbi.nlm.nih.gov/pubmed/35439355 http://dx.doi.org/10.14814/phy2.15257 |
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