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Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits

Animals’ ability to demonstrate both stereotyped and adaptive locomotor behavior is largely dependent on the interplay between centrally generated motor patterns and the sensory inputs that shape them. We utilized a combined experimental and theoretical approach to investigate the relative importanc...

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Autores principales: Fuchs, Einat, Holmes, Philip, Kiemel, Tim, Ayali, Amir
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043608/
https://www.ncbi.nlm.nih.gov/pubmed/21369365
http://dx.doi.org/10.3389/fncir.2010.00125
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author Fuchs, Einat
Holmes, Philip
Kiemel, Tim
Ayali, Amir
author_facet Fuchs, Einat
Holmes, Philip
Kiemel, Tim
Ayali, Amir
author_sort Fuchs, Einat
collection PubMed
description Animals’ ability to demonstrate both stereotyped and adaptive locomotor behavior is largely dependent on the interplay between centrally generated motor patterns and the sensory inputs that shape them. We utilized a combined experimental and theoretical approach to investigate the relative importance of CPG interconnections vs. intersegmental afferents in the cockroach: an animal that is renowned for rapid and stable locomotion. We simultaneously recorded coxal levator and depressor motor neurons (MN) in the thoracic ganglia of Periplaneta americana, while sensory feedback was completely blocked or allowed only from one intact stepping leg. In the absence of sensory feedback, we observed a coordination pattern with consistent phase relationship that shares similarities with a double-tripod gait, suggesting central, feedforward control. This intersegmental coordination pattern was then reinforced in the presence of sensory feedback from a single stepping leg. Specifically, we report on transient stabilization of phase differences between activity recorded in the middle and hind thoracic MN following individual front-leg steps, suggesting a role for afferent phasic information in the coordination of motor circuits at the different hemiganglia. Data were further analyzed using stochastic models of coupled oscillators and maximum likelihood techniques to estimate underlying physiological parameters, such as uncoupled endogenous frequencies of hemisegmental oscillators and coupling strengths and directions. We found that descending ipsilateral coupling is stronger than ascending coupling, while left–right coupling in both the meso- and meta-thoracic ganglia appear to be symmetrical. We discuss these results in comparison with recent findings in stick insects that share similar neural and body architectures, and argue that the two species may exemplify opposite extremes of a fast–slow locomotion continuum, mediated through different intersegment coordination strategies.
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spelling pubmed-30436082011-03-02 Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits Fuchs, Einat Holmes, Philip Kiemel, Tim Ayali, Amir Front Neural Circuits Neuroscience Animals’ ability to demonstrate both stereotyped and adaptive locomotor behavior is largely dependent on the interplay between centrally generated motor patterns and the sensory inputs that shape them. We utilized a combined experimental and theoretical approach to investigate the relative importance of CPG interconnections vs. intersegmental afferents in the cockroach: an animal that is renowned for rapid and stable locomotion. We simultaneously recorded coxal levator and depressor motor neurons (MN) in the thoracic ganglia of Periplaneta americana, while sensory feedback was completely blocked or allowed only from one intact stepping leg. In the absence of sensory feedback, we observed a coordination pattern with consistent phase relationship that shares similarities with a double-tripod gait, suggesting central, feedforward control. This intersegmental coordination pattern was then reinforced in the presence of sensory feedback from a single stepping leg. Specifically, we report on transient stabilization of phase differences between activity recorded in the middle and hind thoracic MN following individual front-leg steps, suggesting a role for afferent phasic information in the coordination of motor circuits at the different hemiganglia. Data were further analyzed using stochastic models of coupled oscillators and maximum likelihood techniques to estimate underlying physiological parameters, such as uncoupled endogenous frequencies of hemisegmental oscillators and coupling strengths and directions. We found that descending ipsilateral coupling is stronger than ascending coupling, while left–right coupling in both the meso- and meta-thoracic ganglia appear to be symmetrical. We discuss these results in comparison with recent findings in stick insects that share similar neural and body architectures, and argue that the two species may exemplify opposite extremes of a fast–slow locomotion continuum, mediated through different intersegment coordination strategies. Frontiers Research Foundation 2011-01-20 /pmc/articles/PMC3043608/ /pubmed/21369365 http://dx.doi.org/10.3389/fncir.2010.00125 Text en Copyright © 2011 Fuchs, Holmes, Kiemel and Ayali. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and Frontiers Media SA, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Fuchs, Einat
Holmes, Philip
Kiemel, Tim
Ayali, Amir
Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits
title Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits
title_full Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits
title_fullStr Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits
title_full_unstemmed Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits
title_short Intersegmental Coordination of Cockroach Locomotion: Adaptive Control of Centrally Coupled Pattern Generator Circuits
title_sort intersegmental coordination of cockroach locomotion: adaptive control of centrally coupled pattern generator circuits
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043608/
https://www.ncbi.nlm.nih.gov/pubmed/21369365
http://dx.doi.org/10.3389/fncir.2010.00125
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