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Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test
Human studies of brain stimulation have demonstrated modulatory effects on the perception of pain. However, whether the primary somatosensory cortical activity is associated with antinociceptive responses remains unknown. Therefore, we examined the antinociceptive effects of neuronal activity evoked...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Brain and Neural Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403911/ https://www.ncbi.nlm.nih.gov/pubmed/28442945 http://dx.doi.org/10.5607/en.2017.26.2.90 |
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author | Lee, Soohyun Hwang, Eunjin Lee, Dongmyeong Choi, Jee Hyun |
author_facet | Lee, Soohyun Hwang, Eunjin Lee, Dongmyeong Choi, Jee Hyun |
author_sort | Lee, Soohyun |
collection | PubMed |
description | Human studies of brain stimulation have demonstrated modulatory effects on the perception of pain. However, whether the primary somatosensory cortical activity is associated with antinociceptive responses remains unknown. Therefore, we examined the antinociceptive effects of neuronal activity evoked by optogenetic stimulation of primary somatosensory cortex. Optogenetic transgenic mice were subjected to continuous or pulse-train optogenetic stimulation of the primary somatosensory cortex at frequencies of 15, 30, and 40 Hz, during a tail clip test. Reaction time was measured using a digital high-speed video camera. Pulse-train optogenetic stimulation of primary somatosensory cortex showed a delayed pain response with respect to a tail clip, whereas no significant change in reaction time was observed with continuous stimulation. In response to the pulse-train stimulation, video monitoring and local field potential recording revealed associated paw movement and sensorimotor rhythms, respectively. Our results show that optogenetic stimulation of primary somatosensory cortex at beta and gamma frequencies blocks transmission of pain signals in tail clip test. |
format | Online Article Text |
id | pubmed-5403911 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Korean Society for Brain and Neural Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54039112017-04-25 Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test Lee, Soohyun Hwang, Eunjin Lee, Dongmyeong Choi, Jee Hyun Exp Neurobiol Original Article Human studies of brain stimulation have demonstrated modulatory effects on the perception of pain. However, whether the primary somatosensory cortical activity is associated with antinociceptive responses remains unknown. Therefore, we examined the antinociceptive effects of neuronal activity evoked by optogenetic stimulation of primary somatosensory cortex. Optogenetic transgenic mice were subjected to continuous or pulse-train optogenetic stimulation of the primary somatosensory cortex at frequencies of 15, 30, and 40 Hz, during a tail clip test. Reaction time was measured using a digital high-speed video camera. Pulse-train optogenetic stimulation of primary somatosensory cortex showed a delayed pain response with respect to a tail clip, whereas no significant change in reaction time was observed with continuous stimulation. In response to the pulse-train stimulation, video monitoring and local field potential recording revealed associated paw movement and sensorimotor rhythms, respectively. Our results show that optogenetic stimulation of primary somatosensory cortex at beta and gamma frequencies blocks transmission of pain signals in tail clip test. The Korean Society for Brain and Neural Science 2017-04 2017-04-10 /pmc/articles/PMC5403911/ /pubmed/28442945 http://dx.doi.org/10.5607/en.2017.26.2.90 Text en Copyright © Experimental Neurobiology 2017. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Soohyun Hwang, Eunjin Lee, Dongmyeong Choi, Jee Hyun Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test |
title | Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test |
title_full | Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test |
title_fullStr | Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test |
title_full_unstemmed | Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test |
title_short | Pulse-train Stimulation of Primary Somatosensory Cortex Blocks Pain Perception in Tail Clip Test |
title_sort | pulse-train stimulation of primary somatosensory cortex blocks pain perception in tail clip test |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403911/ https://www.ncbi.nlm.nih.gov/pubmed/28442945 http://dx.doi.org/10.5607/en.2017.26.2.90 |
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