Cargando…

Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception

In the anesthetized cat the correlation between the ongoing cord dorsum potentials (CDPs) recorded from different lumbar spinal segments has a non-random structure, suggesting relatively stable patterns of functional connectivity between the dorsal horn neuronal ensembles involved in the generation...

Descripción completa

Detalles Bibliográficos
Autores principales: Martín, Mario, Béjar, Javier, Chávez, Diógenes, Ramírez-Morales, Adrian, Hernández, Edson, Moreno, Leonardo, Contreras-Hernández, Enrique, Glusman, Silvio, Cortés, Ulises, Rudomin, Pablo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775247/
https://www.ncbi.nlm.nih.gov/pubmed/31616259
http://dx.doi.org/10.3389/fnsys.2019.00047
_version_ 1783456200824717312
author Martín, Mario
Béjar, Javier
Chávez, Diógenes
Ramírez-Morales, Adrian
Hernández, Edson
Moreno, Leonardo
Contreras-Hernández, Enrique
Glusman, Silvio
Cortés, Ulises
Rudomin, Pablo
author_facet Martín, Mario
Béjar, Javier
Chávez, Diógenes
Ramírez-Morales, Adrian
Hernández, Edson
Moreno, Leonardo
Contreras-Hernández, Enrique
Glusman, Silvio
Cortés, Ulises
Rudomin, Pablo
author_sort Martín, Mario
collection PubMed
description In the anesthetized cat the correlation between the ongoing cord dorsum potentials (CDPs) recorded from different lumbar spinal segments has a non-random structure, suggesting relatively stable patterns of functional connectivity between the dorsal horn neuronal ensembles involved in the generation of these potentials. During the nociception induced by the intradermic injection of capsaicin, the patterns of segmental correlation between the spontaneous CDPs acquire other non-random configurations that are temporarily reversed to their pre-capsaicin state by the systemic injection of lidocaine, a procedure known to decrease the manifestation of neuropathic pain in both animals and humans. We have now extended these studies and utilized machine learning for the automatic extraction and selection of particular classes of CDPs according to their shapes and amplitudes. By using a Markovian analysis, we disclosed the transitions between the different kinds of CDPs induced by capsaicin and lidocaine and constructed a global model based on the changes in the behavior of the CDPs generated along the whole set of lumbar segments. This allowed the identification of the different states of functional connectivity within the whole ensemble of dorsal horn neurones attained during nociception and their transitory reversal by systemic administration of lidocaine in preparations with the intact neuroaxis and after spinalization. The present observations provide additional information on the state of self-organized criticality that leads to the adaptive behavior of the dorsal horn neuronal networks during nociception and antinociception both shaped by supraspinal descending influences.
format Online
Article
Text
id pubmed-6775247
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-67752472019-10-15 Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception Martín, Mario Béjar, Javier Chávez, Diógenes Ramírez-Morales, Adrian Hernández, Edson Moreno, Leonardo Contreras-Hernández, Enrique Glusman, Silvio Cortés, Ulises Rudomin, Pablo Front Syst Neurosci Neuroscience In the anesthetized cat the correlation between the ongoing cord dorsum potentials (CDPs) recorded from different lumbar spinal segments has a non-random structure, suggesting relatively stable patterns of functional connectivity between the dorsal horn neuronal ensembles involved in the generation of these potentials. During the nociception induced by the intradermic injection of capsaicin, the patterns of segmental correlation between the spontaneous CDPs acquire other non-random configurations that are temporarily reversed to their pre-capsaicin state by the systemic injection of lidocaine, a procedure known to decrease the manifestation of neuropathic pain in both animals and humans. We have now extended these studies and utilized machine learning for the automatic extraction and selection of particular classes of CDPs according to their shapes and amplitudes. By using a Markovian analysis, we disclosed the transitions between the different kinds of CDPs induced by capsaicin and lidocaine and constructed a global model based on the changes in the behavior of the CDPs generated along the whole set of lumbar segments. This allowed the identification of the different states of functional connectivity within the whole ensemble of dorsal horn neurones attained during nociception and their transitory reversal by systemic administration of lidocaine in preparations with the intact neuroaxis and after spinalization. The present observations provide additional information on the state of self-organized criticality that leads to the adaptive behavior of the dorsal horn neuronal networks during nociception and antinociception both shaped by supraspinal descending influences. Frontiers Media S.A. 2019-09-26 /pmc/articles/PMC6775247/ /pubmed/31616259 http://dx.doi.org/10.3389/fnsys.2019.00047 Text en Copyright © 2019 Martín, Béjar, Chávez, Ramírez-Morales, Hernández, Moreno, Contreras-Hernández, Glusman, Cortés and Rudomin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Martín, Mario
Béjar, Javier
Chávez, Diógenes
Ramírez-Morales, Adrian
Hernández, Edson
Moreno, Leonardo
Contreras-Hernández, Enrique
Glusman, Silvio
Cortés, Ulises
Rudomin, Pablo
Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception
title Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception
title_full Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception
title_fullStr Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception
title_full_unstemmed Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception
title_short Supraspinal Shaping of Adaptive Transitions in the State of Functional Connectivity Between Segmentally Distributed Dorsal Horn Neuronal Populations in Response to Nociception and Antinociception
title_sort supraspinal shaping of adaptive transitions in the state of functional connectivity between segmentally distributed dorsal horn neuronal populations in response to nociception and antinociception
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775247/
https://www.ncbi.nlm.nih.gov/pubmed/31616259
http://dx.doi.org/10.3389/fnsys.2019.00047
work_keys_str_mv AT martinmario supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT bejarjavier supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT chavezdiogenes supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT ramirezmoralesadrian supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT hernandezedson supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT morenoleonardo supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT contrerashernandezenrique supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT glusmansilvio supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT cortesulises supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception
AT rudominpablo supraspinalshapingofadaptivetransitionsinthestateoffunctionalconnectivitybetweensegmentallydistributeddorsalhornneuronalpopulationsinresponsetonociceptionandantinociception