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Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats

Transcranial direct current stimulation (tDCS) is an emerging, noninvasive technique of neurostimulation for treating pain. However, the mechanisms and pathways involved in its analgesic effects are poorly understood. Therefore, we investigated the effects of direct current stimulation (DCS) on ther...

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Autores principales: Dimov, Luiz Fabio, Franciosi, Adriano Cardozo, Campos, Ana Carolina Pinheiro, Brunoni, André Russowsky, Pagano, Rosana Lima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829148/
https://www.ncbi.nlm.nih.gov/pubmed/27071073
http://dx.doi.org/10.1371/journal.pone.0153506
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author Dimov, Luiz Fabio
Franciosi, Adriano Cardozo
Campos, Ana Carolina Pinheiro
Brunoni, André Russowsky
Pagano, Rosana Lima
author_facet Dimov, Luiz Fabio
Franciosi, Adriano Cardozo
Campos, Ana Carolina Pinheiro
Brunoni, André Russowsky
Pagano, Rosana Lima
author_sort Dimov, Luiz Fabio
collection PubMed
description Transcranial direct current stimulation (tDCS) is an emerging, noninvasive technique of neurostimulation for treating pain. However, the mechanisms and pathways involved in its analgesic effects are poorly understood. Therefore, we investigated the effects of direct current stimulation (DCS) on thermal and mechanical nociceptive thresholds and on the activation of the midbrain periaqueductal gray (PAG) and the dorsal horn of the spinal cord (DHSC) in rats; these central nervous system areas are associated with pain processing. Male Wistar rats underwent cathodal DCS of the motor cortex and, while still under stimulation, were evaluated using tail-flick and paw pressure nociceptive tests. Sham stimulation and naive rats were used as controls. We used a randomized design; the assays were not blinded to the experimenter. Immunoreactivity of the early growth response gene 1 (Egr-1), which is a marker of neuronal activation, was evaluated in the PAG and DHSC, and enkephalin immunoreactivity was evaluated in the DHSC. DCS did not change the thermal nociceptive threshold; however, it increased the mechanical nociceptive threshold of both hind paws compared with that of controls, characterizing a topographical effect. DCS decreased the Egr-1 labeling in the PAG and DHSC as well as the immunoreactivity of spinal enkephalin. Altogether, the data suggest that DCS disinhibits the midbrain descending analgesic pathway, consequently inhibiting spinal nociceptive neurons and causing an increase in the nociceptive threshold. This study reinforces the idea that the motor cortex participates in the neurocircuitry that is involved in analgesia and further clarifies the mechanisms of action of tDCS in pain treatment.
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spelling pubmed-48291482016-04-22 Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats Dimov, Luiz Fabio Franciosi, Adriano Cardozo Campos, Ana Carolina Pinheiro Brunoni, André Russowsky Pagano, Rosana Lima PLoS One Research Article Transcranial direct current stimulation (tDCS) is an emerging, noninvasive technique of neurostimulation for treating pain. However, the mechanisms and pathways involved in its analgesic effects are poorly understood. Therefore, we investigated the effects of direct current stimulation (DCS) on thermal and mechanical nociceptive thresholds and on the activation of the midbrain periaqueductal gray (PAG) and the dorsal horn of the spinal cord (DHSC) in rats; these central nervous system areas are associated with pain processing. Male Wistar rats underwent cathodal DCS of the motor cortex and, while still under stimulation, were evaluated using tail-flick and paw pressure nociceptive tests. Sham stimulation and naive rats were used as controls. We used a randomized design; the assays were not blinded to the experimenter. Immunoreactivity of the early growth response gene 1 (Egr-1), which is a marker of neuronal activation, was evaluated in the PAG and DHSC, and enkephalin immunoreactivity was evaluated in the DHSC. DCS did not change the thermal nociceptive threshold; however, it increased the mechanical nociceptive threshold of both hind paws compared with that of controls, characterizing a topographical effect. DCS decreased the Egr-1 labeling in the PAG and DHSC as well as the immunoreactivity of spinal enkephalin. Altogether, the data suggest that DCS disinhibits the midbrain descending analgesic pathway, consequently inhibiting spinal nociceptive neurons and causing an increase in the nociceptive threshold. This study reinforces the idea that the motor cortex participates in the neurocircuitry that is involved in analgesia and further clarifies the mechanisms of action of tDCS in pain treatment. Public Library of Science 2016-04-12 /pmc/articles/PMC4829148/ /pubmed/27071073 http://dx.doi.org/10.1371/journal.pone.0153506 Text en © 2016 Dimov et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dimov, Luiz Fabio
Franciosi, Adriano Cardozo
Campos, Ana Carolina Pinheiro
Brunoni, André Russowsky
Pagano, Rosana Lima
Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats
title Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats
title_full Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats
title_fullStr Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats
title_full_unstemmed Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats
title_short Top-Down Effect of Direct Current Stimulation on the Nociceptive Response of Rats
title_sort top-down effect of direct current stimulation on the nociceptive response of rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829148/
https://www.ncbi.nlm.nih.gov/pubmed/27071073
http://dx.doi.org/10.1371/journal.pone.0153506
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