Cargando…
Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients
The study presents a novel approach of programing pain inhibition in chronic pain patients based on the hypothesis that pain perception is modulated by dysfunctional dorsal medial nucleus tractus solitarii (dmNTS) reflex arcs that produce diminished baroreflex sensitivity (BRS) resulting from a cond...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605536/ https://www.ncbi.nlm.nih.gov/pubmed/36294542 http://dx.doi.org/10.3390/jcm11206220 |
_version_ | 1784818091492900864 |
---|---|
author | Thieme, Kati Jung, Kathrin Mathys, Marc G. Gracely, Richard H. Turk, Dennis C. |
author_facet | Thieme, Kati Jung, Kathrin Mathys, Marc G. Gracely, Richard H. Turk, Dennis C. |
author_sort | Thieme, Kati |
collection | PubMed |
description | The study presents a novel approach of programing pain inhibition in chronic pain patients based on the hypothesis that pain perception is modulated by dysfunctional dorsal medial nucleus tractus solitarii (dmNTS) reflex arcs that produce diminished baroreflex sensitivity (BRS) resulting from a conditioned response. This study tested whether administration of noxious and non-noxious electrical stimuli synchronized with the cardiac cycle resets BRS, reestablishing pain inhibition. A total of 30 pain-free normotensives controls (NC) and 32 normotensives fibromyalgia (FM) patients received two, ≈8 min-epochs of cardiac-gated, peripheral electrical stimuli. Non-painful and painful electrical stimuli were synchronized to the cardiac cycle as the neuromodulation experimental protocol (EP) with two control conditions (CC1, CC2). BRS, heart-rate-variability (HRV), pain threshold and tolerance, and clinical pain intensity were assessed. Reduced BRS in FM at baseline increased by 41% during two, ≈8 min-epochs of stimulation. Thresholds in FM increased significantly during the experimental protocol (all Ps < 0.001) as did HRV. FM levels of clinical pain significantly decreased by 35.52% during the experimental protocol but not during control stimulations (p < 0.001). Baroreceptor training may reduce FM pain by BRS-mediated effects on intrinsic pain regulatory systems and autonomic responses. |
format | Online Article Text |
id | pubmed-9605536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96055362022-10-27 Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients Thieme, Kati Jung, Kathrin Mathys, Marc G. Gracely, Richard H. Turk, Dennis C. J Clin Med Article The study presents a novel approach of programing pain inhibition in chronic pain patients based on the hypothesis that pain perception is modulated by dysfunctional dorsal medial nucleus tractus solitarii (dmNTS) reflex arcs that produce diminished baroreflex sensitivity (BRS) resulting from a conditioned response. This study tested whether administration of noxious and non-noxious electrical stimuli synchronized with the cardiac cycle resets BRS, reestablishing pain inhibition. A total of 30 pain-free normotensives controls (NC) and 32 normotensives fibromyalgia (FM) patients received two, ≈8 min-epochs of cardiac-gated, peripheral electrical stimuli. Non-painful and painful electrical stimuli were synchronized to the cardiac cycle as the neuromodulation experimental protocol (EP) with two control conditions (CC1, CC2). BRS, heart-rate-variability (HRV), pain threshold and tolerance, and clinical pain intensity were assessed. Reduced BRS in FM at baseline increased by 41% during two, ≈8 min-epochs of stimulation. Thresholds in FM increased significantly during the experimental protocol (all Ps < 0.001) as did HRV. FM levels of clinical pain significantly decreased by 35.52% during the experimental protocol but not during control stimulations (p < 0.001). Baroreceptor training may reduce FM pain by BRS-mediated effects on intrinsic pain regulatory systems and autonomic responses. MDPI 2022-10-21 /pmc/articles/PMC9605536/ /pubmed/36294542 http://dx.doi.org/10.3390/jcm11206220 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Thieme, Kati Jung, Kathrin Mathys, Marc G. Gracely, Richard H. Turk, Dennis C. Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients |
title | Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients |
title_full | Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients |
title_fullStr | Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients |
title_full_unstemmed | Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients |
title_short | Cardiac-Gated Neuromodulation Increased Baroreflex Sensitivity and Reduced Pain Sensitivity in Female Fibromyalgia Patients |
title_sort | cardiac-gated neuromodulation increased baroreflex sensitivity and reduced pain sensitivity in female fibromyalgia patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605536/ https://www.ncbi.nlm.nih.gov/pubmed/36294542 http://dx.doi.org/10.3390/jcm11206220 |
work_keys_str_mv | AT thiemekati cardiacgatedneuromodulationincreasedbaroreflexsensitivityandreducedpainsensitivityinfemalefibromyalgiapatients AT jungkathrin cardiacgatedneuromodulationincreasedbaroreflexsensitivityandreducedpainsensitivityinfemalefibromyalgiapatients AT mathysmarcg cardiacgatedneuromodulationincreasedbaroreflexsensitivityandreducedpainsensitivityinfemalefibromyalgiapatients AT gracelyrichardh cardiacgatedneuromodulationincreasedbaroreflexsensitivityandreducedpainsensitivityinfemalefibromyalgiapatients AT turkdennisc cardiacgatedneuromodulationincreasedbaroreflexsensitivityandreducedpainsensitivityinfemalefibromyalgiapatients |