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Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions

Despite advancements in pharmacotherapies, glycemia is poorly controlled in type 2 diabetic patients. As the vagus nerve regulates energy metabolism, here we evaluated the effect various electrical vagus nerve stimulation strategies have on glycemia and glucose‐regulating hormones, as a first step t...

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Autores principales: Payne, Sophie C., Ward, Glenn, MacIsaac, Richard J., Hyakumura, Tomoko, Fallon, James B., Villalobos, Joel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280012/
https://www.ncbi.nlm.nih.gov/pubmed/32512650
http://dx.doi.org/10.14814/phy2.14479
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author Payne, Sophie C.
Ward, Glenn
MacIsaac, Richard J.
Hyakumura, Tomoko
Fallon, James B.
Villalobos, Joel
author_facet Payne, Sophie C.
Ward, Glenn
MacIsaac, Richard J.
Hyakumura, Tomoko
Fallon, James B.
Villalobos, Joel
author_sort Payne, Sophie C.
collection PubMed
description Despite advancements in pharmacotherapies, glycemia is poorly controlled in type 2 diabetic patients. As the vagus nerve regulates energy metabolism, here we evaluated the effect various electrical vagus nerve stimulation strategies have on glycemia and glucose‐regulating hormones, as a first step to developing a novel therapy of type 2 diabetes. Sprague–Dawley rats were anesthetized, the abdominal (anterior) vagus nerve implanted, and various stimulation strategies applied to the nerve: (a) 15 Hz; (b) 4 kHz, or 40 kHz and; (c) a combination of 15 Hz and 40 kHz to directionally activate afferent or efferent vagal fibers. Following a glucose bolus (500 mg/kg, I.V.), stimulation strategies were applied (60 min) and serial blood samples taken. No stimulation was used as a crossover control sequence. Applying 15 Hz stimulation significantly increased glucose (+2.9 ± 0.2 mM·hr, p = .015) and glucagon (+17.1 ± 8.0 pg·hr/ml, p = .022), compared to no stimulation. Application of 4 kHz stimulation also significantly increased glucose levels (+1.5 ± 0.5 mM·hr, p = .049), while 40 kHz frequency stimulation resulted in no changes to glucose levels but did significantly lower glucagon (−12.3 ± 1.1 pg·hr/ml, p = .0009). Directional afferent stimulation increased glucose (+2.4 ± 1.5 mM·hr) and glucagon levels (+39.5 ± 15.0 pg·hr/ml). Despite hyperglycemia resulting when VNS, aVNS, and 4 kHz stimulation strategies were applied, the changes in insulin levels were not significant (p ≥ .05). In summary, vagus nerve stimulation modulates glycemia by effecting glucagon and insulin secretions, and high‐frequency 40 kHz stimulation may have potential application for the treatment of type 2 diabetes.
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spelling pubmed-72800122020-06-10 Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions Payne, Sophie C. Ward, Glenn MacIsaac, Richard J. Hyakumura, Tomoko Fallon, James B. Villalobos, Joel Physiol Rep Original Articles Despite advancements in pharmacotherapies, glycemia is poorly controlled in type 2 diabetic patients. As the vagus nerve regulates energy metabolism, here we evaluated the effect various electrical vagus nerve stimulation strategies have on glycemia and glucose‐regulating hormones, as a first step to developing a novel therapy of type 2 diabetes. Sprague–Dawley rats were anesthetized, the abdominal (anterior) vagus nerve implanted, and various stimulation strategies applied to the nerve: (a) 15 Hz; (b) 4 kHz, or 40 kHz and; (c) a combination of 15 Hz and 40 kHz to directionally activate afferent or efferent vagal fibers. Following a glucose bolus (500 mg/kg, I.V.), stimulation strategies were applied (60 min) and serial blood samples taken. No stimulation was used as a crossover control sequence. Applying 15 Hz stimulation significantly increased glucose (+2.9 ± 0.2 mM·hr, p = .015) and glucagon (+17.1 ± 8.0 pg·hr/ml, p = .022), compared to no stimulation. Application of 4 kHz stimulation also significantly increased glucose levels (+1.5 ± 0.5 mM·hr, p = .049), while 40 kHz frequency stimulation resulted in no changes to glucose levels but did significantly lower glucagon (−12.3 ± 1.1 pg·hr/ml, p = .0009). Directional afferent stimulation increased glucose (+2.4 ± 1.5 mM·hr) and glucagon levels (+39.5 ± 15.0 pg·hr/ml). Despite hyperglycemia resulting when VNS, aVNS, and 4 kHz stimulation strategies were applied, the changes in insulin levels were not significant (p ≥ .05). In summary, vagus nerve stimulation modulates glycemia by effecting glucagon and insulin secretions, and high‐frequency 40 kHz stimulation may have potential application for the treatment of type 2 diabetes. John Wiley and Sons Inc. 2020-06-08 /pmc/articles/PMC7280012/ /pubmed/32512650 http://dx.doi.org/10.14814/phy2.14479 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://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
MacIsaac, Richard J.
Hyakumura, Tomoko
Fallon, James B.
Villalobos, Joel
Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
title Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
title_full Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
title_fullStr Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
title_full_unstemmed Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
title_short Differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
title_sort differential effects of vagus nerve stimulation strategies on glycemia and pancreatic secretions
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7280012/
https://www.ncbi.nlm.nih.gov/pubmed/32512650
http://dx.doi.org/10.14814/phy2.14479
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