Cargando…

Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles

Electrical coupling is important in rhythm generating systems. We examine its role in circuits controlling locomotion in a simple vertebrate model, the young Xenopus tadpole, where the hindbrain and spinal cord excitatory descending interneurons (dINs) that drive and maintain swimming have been char...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Wen-Chang, Roberts, Alan, Soffe, Stephen R
Formato: Texto
Lenguaje:English
Publicado: Blackwell Science Inc 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683956/
https://www.ncbi.nlm.nih.gov/pubmed/19221124
http://dx.doi.org/10.1113/jphysiol.2008.166942
_version_ 1782167157199601664
author Li, Wen-Chang
Roberts, Alan
Soffe, Stephen R
author_facet Li, Wen-Chang
Roberts, Alan
Soffe, Stephen R
author_sort Li, Wen-Chang
collection PubMed
description Electrical coupling is important in rhythm generating systems. We examine its role in circuits controlling locomotion in a simple vertebrate model, the young Xenopus tadpole, where the hindbrain and spinal cord excitatory descending interneurons (dINs) that drive and maintain swimming have been characterised. Using simultaneous paired recordings, we show that most dINs are electrically coupled exclusively to other dINs (DC coupling coefficients ∼8.5%). The coupling shows typical low-pass filtering. We found no evidence that other swimming central pattern generator (CPG) interneurons are coupled to dINs or to each other. Electrical coupling potentials between dINs appear to contribute to their unusually reliable firing during swimming. To investigate the role of electrical coupling in swimming, we evaluated the specificity of gap junction blockers (18-β-GA, carbenoxolone, flufenamic acid and heptanol) in paired recordings. 18-β-GA at 40–60 μm produced substantial (84%) coupling block but few effects on cellular properties. Swimming episodes in 18-β-GA were significantly shortened (to ∼2% of control durations). At the same time, dIN firing reliability fell from nearly 100% to 62% of swimming cycles and spike synchronization weakened. Because dINs drive CPG neuron firing and are critical in maintaining swimming, the weakening of dIN activity could account for the effects of 18-β-GA on swimming. We conclude that electrical coupling among pre motor reticulospinal and spinal dINs, the excitatory interneurons that drive the swimming CPG in the hatchling Xenopus tadpole, may contribute to the maintenance of swimming as well as synchronization of activity.
format Text
id pubmed-2683956
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Blackwell Science Inc
record_format MEDLINE/PubMed
spelling pubmed-26839562009-06-11 Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles Li, Wen-Chang Roberts, Alan Soffe, Stephen R J Physiol Neuroscience Electrical coupling is important in rhythm generating systems. We examine its role in circuits controlling locomotion in a simple vertebrate model, the young Xenopus tadpole, where the hindbrain and spinal cord excitatory descending interneurons (dINs) that drive and maintain swimming have been characterised. Using simultaneous paired recordings, we show that most dINs are electrically coupled exclusively to other dINs (DC coupling coefficients ∼8.5%). The coupling shows typical low-pass filtering. We found no evidence that other swimming central pattern generator (CPG) interneurons are coupled to dINs or to each other. Electrical coupling potentials between dINs appear to contribute to their unusually reliable firing during swimming. To investigate the role of electrical coupling in swimming, we evaluated the specificity of gap junction blockers (18-β-GA, carbenoxolone, flufenamic acid and heptanol) in paired recordings. 18-β-GA at 40–60 μm produced substantial (84%) coupling block but few effects on cellular properties. Swimming episodes in 18-β-GA were significantly shortened (to ∼2% of control durations). At the same time, dIN firing reliability fell from nearly 100% to 62% of swimming cycles and spike synchronization weakened. Because dINs drive CPG neuron firing and are critical in maintaining swimming, the weakening of dIN activity could account for the effects of 18-β-GA on swimming. We conclude that electrical coupling among pre motor reticulospinal and spinal dINs, the excitatory interneurons that drive the swimming CPG in the hatchling Xenopus tadpole, may contribute to the maintenance of swimming as well as synchronization of activity. Blackwell Science Inc 2009-04-15 2009-02-16 /pmc/articles/PMC2683956/ /pubmed/19221124 http://dx.doi.org/10.1113/jphysiol.2008.166942 Text en Journal compilation © 2009 The Physiological Society
spellingShingle Neuroscience
Li, Wen-Chang
Roberts, Alan
Soffe, Stephen R
Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles
title Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles
title_full Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles
title_fullStr Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles
title_full_unstemmed Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles
title_short Locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young Xenopus tadpoles
title_sort locomotor rhythm maintenance: electrical coupling among premotor excitatory interneurons in the brainstem and spinal cord of young xenopus tadpoles
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683956/
https://www.ncbi.nlm.nih.gov/pubmed/19221124
http://dx.doi.org/10.1113/jphysiol.2008.166942
work_keys_str_mv AT liwenchang locomotorrhythmmaintenanceelectricalcouplingamongpremotorexcitatoryinterneuronsinthebrainstemandspinalcordofyoungxenopustadpoles
AT robertsalan locomotorrhythmmaintenanceelectricalcouplingamongpremotorexcitatoryinterneuronsinthebrainstemandspinalcordofyoungxenopustadpoles
AT soffestephenr locomotorrhythmmaintenanceelectricalcouplingamongpremotorexcitatoryinterneuronsinthebrainstemandspinalcordofyoungxenopustadpoles