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Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD

Studies have indicated that vagus nerve stimulation (VNS) enhances extinction learning in rodent models. Here, we investigated if pairing VNS with the conditioned stimulus is required for the enhancing effects of VNS. Adult Sprague–Dawley rats were exposed to intense stress followed by fear conditio...

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Autores principales: Souza, Rimenez R., Powers, Mark B., Rennaker, Robert L., McIntyre, Christa K., Hays, Seth A., Kilgard, Michael P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530175/
https://www.ncbi.nlm.nih.gov/pubmed/36192564
http://dx.doi.org/10.1038/s41598-022-20301-9
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author Souza, Rimenez R.
Powers, Mark B.
Rennaker, Robert L.
McIntyre, Christa K.
Hays, Seth A.
Kilgard, Michael P.
author_facet Souza, Rimenez R.
Powers, Mark B.
Rennaker, Robert L.
McIntyre, Christa K.
Hays, Seth A.
Kilgard, Michael P.
author_sort Souza, Rimenez R.
collection PubMed
description Studies have indicated that vagus nerve stimulation (VNS) enhances extinction learning in rodent models. Here, we investigated if pairing VNS with the conditioned stimulus is required for the enhancing effects of VNS. Adult Sprague–Dawley rats were exposed to intense stress followed by fear conditioning training to produce resistant fear. Rats were then implanted with a cuff electrode around the left vagus. After recovery, rats underwent extinction training paired with VNS (0.5 s, 0.8 mA, 100 µs, and 30 Hz) or with Sham VNS (0 mA). VNS rats were randomized into the following subgroups: During VNS (delivered during presentations of the conditioned stimulus, CS), Between VNS (delivered between CS presentations), Continuous VNS (delivered during the entire extinction session), and Dispersed VNS (delivered at longer inter-stimulation intervals across the extinction session). Sham VNS rats failed to extinguish the conditioned fear response over 5 days of repeated exposure to the CS. Rats that received Between or Dispersed VNS showed modest improvement in conditioned fear at the retention test. During and Continuous VNS groups displayed the greatest reduction in conditioned fear. These findings indicate that delivering VNS paired precisely with CS presentations or continuously throughout extinction promotes the maximum enhancement in extinction learning.
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spelling pubmed-95301752022-10-05 Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD Souza, Rimenez R. Powers, Mark B. Rennaker, Robert L. McIntyre, Christa K. Hays, Seth A. Kilgard, Michael P. Sci Rep Article Studies have indicated that vagus nerve stimulation (VNS) enhances extinction learning in rodent models. Here, we investigated if pairing VNS with the conditioned stimulus is required for the enhancing effects of VNS. Adult Sprague–Dawley rats were exposed to intense stress followed by fear conditioning training to produce resistant fear. Rats were then implanted with a cuff electrode around the left vagus. After recovery, rats underwent extinction training paired with VNS (0.5 s, 0.8 mA, 100 µs, and 30 Hz) or with Sham VNS (0 mA). VNS rats were randomized into the following subgroups: During VNS (delivered during presentations of the conditioned stimulus, CS), Between VNS (delivered between CS presentations), Continuous VNS (delivered during the entire extinction session), and Dispersed VNS (delivered at longer inter-stimulation intervals across the extinction session). Sham VNS rats failed to extinguish the conditioned fear response over 5 days of repeated exposure to the CS. Rats that received Between or Dispersed VNS showed modest improvement in conditioned fear at the retention test. During and Continuous VNS groups displayed the greatest reduction in conditioned fear. These findings indicate that delivering VNS paired precisely with CS presentations or continuously throughout extinction promotes the maximum enhancement in extinction learning. Nature Publishing Group UK 2022-10-03 /pmc/articles/PMC9530175/ /pubmed/36192564 http://dx.doi.org/10.1038/s41598-022-20301-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Souza, Rimenez R.
Powers, Mark B.
Rennaker, Robert L.
McIntyre, Christa K.
Hays, Seth A.
Kilgard, Michael P.
Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD
title Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD
title_full Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD
title_fullStr Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD
title_full_unstemmed Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD
title_short Timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of PTSD
title_sort timing of vagus nerve stimulation during fear extinction determines efficacy in a rat model of ptsd
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9530175/
https://www.ncbi.nlm.nih.gov/pubmed/36192564
http://dx.doi.org/10.1038/s41598-022-20301-9
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