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Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats
Background: The spinal cord’s central pattern generators (CPGs) have been explained by the symmetrical half-center hypothesis, the bursts generator, computational models, and more recently by connectome circuits. Asymmetrical models, at odds with the half-center paradigm, are composed of extensor an...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056700/ https://www.ncbi.nlm.nih.gov/pubmed/32174815 http://dx.doi.org/10.3389/fncir.2020.00001 |
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author | Aguilar Garcia, Irene Guadalupe Dueñas-Jiménez, Judith Marcela Castillo, Luis Osuna-Carrasco, Laura Paulina De La Torre Valdovinos, Braniff Castañeda-Arellano, Rolando López-Ruiz, Jose Roberto Toro-Castillo, Carmen Treviño, Mario Mendizabal-Ruiz, Gerardo Duenas-Jimenez, Sergio Horacio |
author_facet | Aguilar Garcia, Irene Guadalupe Dueñas-Jiménez, Judith Marcela Castillo, Luis Osuna-Carrasco, Laura Paulina De La Torre Valdovinos, Braniff Castañeda-Arellano, Rolando López-Ruiz, Jose Roberto Toro-Castillo, Carmen Treviño, Mario Mendizabal-Ruiz, Gerardo Duenas-Jimenez, Sergio Horacio |
author_sort | Aguilar Garcia, Irene Guadalupe |
collection | PubMed |
description | Background: The spinal cord’s central pattern generators (CPGs) have been explained by the symmetrical half-center hypothesis, the bursts generator, computational models, and more recently by connectome circuits. Asymmetrical models, at odds with the half-center paradigm, are composed of extensor and flexor CPG modules. Other models include not only flexor and extensor motoneurons but also motoneuron pools controlling biarticular muscles. It is unknown whether a preferred model can explain some particularities that fictive scratching (FS) in the cat presents. The first aim of this study was to investigate FS patterns considering the aiming and the rhythmic periods, and second, to examine the effects of serotonin (5HT) on and segmental inputs to FS. Methods: The experiments were carried out first in brain cortex-ablated cats (BCAC), then spinalized (SC), and for the midcollicular (MCC) preparation. Subjects were immobilized and the peripheral nerves were used to elicit the Monosynaptic reflex (MR), to modify the scratching patterns and for electroneurogram recordings. Results: In BCAC, FS was produced by pinna stimulation and, in some cases, by serotonin. The scratching aiming phase (AP) initiates with the activation of either flexor or extensor motoneurons. Serotonin application during the AP produced simultaneous extensor and flexor bursts. Furthermore, WAY 100635 (5HT1A antagonist) produced a brief burst in the tibialis anterior (TA) nerve, followed by a reduction in its electroneurogram (ENG), while the soleus ENG remained silent. In SC, rhythmic phase (RP) activity was recorded in the soleus motoneurons. Serotonin or WAY produced FS bouts. The electrical stimulation of Ia afferent fibers produced heteronymous MRes waxing and waning during the scratch cycle. In MCC, FS began with flexor activity. Electrical stimulation of either deep peroneus (DP) or superficial peroneus (SP) nerves increased the duration of the TA electroneurogram. Medial gastrocnemius (MG) stretching or MG nerve electrical stimulation produced a reduction in the TA electroneurogram and an initial MG extensor burst. MRes waxed and waned during the scratch cycle. Conclusion: Descending pathways and segmental afferent fibers, as well as 5-HT and WAY, can change the FS pattern. To our understanding, the half-center hypothesis is the most suitable for explaining the AP in MCC. |
format | Online Article Text |
id | pubmed-7056700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70567002020-03-13 Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats Aguilar Garcia, Irene Guadalupe Dueñas-Jiménez, Judith Marcela Castillo, Luis Osuna-Carrasco, Laura Paulina De La Torre Valdovinos, Braniff Castañeda-Arellano, Rolando López-Ruiz, Jose Roberto Toro-Castillo, Carmen Treviño, Mario Mendizabal-Ruiz, Gerardo Duenas-Jimenez, Sergio Horacio Front Neural Circuits Neuroscience Background: The spinal cord’s central pattern generators (CPGs) have been explained by the symmetrical half-center hypothesis, the bursts generator, computational models, and more recently by connectome circuits. Asymmetrical models, at odds with the half-center paradigm, are composed of extensor and flexor CPG modules. Other models include not only flexor and extensor motoneurons but also motoneuron pools controlling biarticular muscles. It is unknown whether a preferred model can explain some particularities that fictive scratching (FS) in the cat presents. The first aim of this study was to investigate FS patterns considering the aiming and the rhythmic periods, and second, to examine the effects of serotonin (5HT) on and segmental inputs to FS. Methods: The experiments were carried out first in brain cortex-ablated cats (BCAC), then spinalized (SC), and for the midcollicular (MCC) preparation. Subjects were immobilized and the peripheral nerves were used to elicit the Monosynaptic reflex (MR), to modify the scratching patterns and for electroneurogram recordings. Results: In BCAC, FS was produced by pinna stimulation and, in some cases, by serotonin. The scratching aiming phase (AP) initiates with the activation of either flexor or extensor motoneurons. Serotonin application during the AP produced simultaneous extensor and flexor bursts. Furthermore, WAY 100635 (5HT1A antagonist) produced a brief burst in the tibialis anterior (TA) nerve, followed by a reduction in its electroneurogram (ENG), while the soleus ENG remained silent. In SC, rhythmic phase (RP) activity was recorded in the soleus motoneurons. Serotonin or WAY produced FS bouts. The electrical stimulation of Ia afferent fibers produced heteronymous MRes waxing and waning during the scratch cycle. In MCC, FS began with flexor activity. Electrical stimulation of either deep peroneus (DP) or superficial peroneus (SP) nerves increased the duration of the TA electroneurogram. Medial gastrocnemius (MG) stretching or MG nerve electrical stimulation produced a reduction in the TA electroneurogram and an initial MG extensor burst. MRes waxed and waned during the scratch cycle. Conclusion: Descending pathways and segmental afferent fibers, as well as 5-HT and WAY, can change the FS pattern. To our understanding, the half-center hypothesis is the most suitable for explaining the AP in MCC. Frontiers Media S.A. 2020-02-27 /pmc/articles/PMC7056700/ /pubmed/32174815 http://dx.doi.org/10.3389/fncir.2020.00001 Text en Copyright © 2020 Aguilar Garcia, Dueñas-Jiménez, Castillo, Osuna-Carrasco, De La Torre Valdovinos, Castañeda-Arellano, López-Ruiz, Toro-Castillo, Treviño, Mendizabal-Ruiz and Duenas-Jimenez. 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 Aguilar Garcia, Irene Guadalupe Dueñas-Jiménez, Judith Marcela Castillo, Luis Osuna-Carrasco, Laura Paulina De La Torre Valdovinos, Braniff Castañeda-Arellano, Rolando López-Ruiz, Jose Roberto Toro-Castillo, Carmen Treviño, Mario Mendizabal-Ruiz, Gerardo Duenas-Jimenez, Sergio Horacio Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats |
title | Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats |
title_full | Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats |
title_fullStr | Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats |
title_full_unstemmed | Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats |
title_short | Fictive Scratching Patterns in Brain Cortex-Ablated, Midcollicular Decerebrate, and Spinal Cats |
title_sort | fictive scratching patterns in brain cortex-ablated, midcollicular decerebrate, and spinal cats |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056700/ https://www.ncbi.nlm.nih.gov/pubmed/32174815 http://dx.doi.org/10.3389/fncir.2020.00001 |
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