Unbound MEDLINE

Activity of Hb9 interneurons during fictive locomotion in mouse spinal cord. The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] Journal article

 
TitleActivity of Hb9 interneurons during fictive locomotion in mouse spinal cord.
Author(s)Kwan AC, Dietz SB, Webb WW, Harris-Warrick RM 
InstitutionSchool of Applied and Engineering Physics, Cornell University, Ithaca, New York 14853, USA.
SourceJ Neurosci 2009 Sep 16; 29(37):11601-13.
MeSHAnalysis of Variance
Animals
Behavior, Animal
Calcium
Dopamine
Electric Stimulation
Functional Laterality
Green Fluorescent Proteins
Homeodomain Proteins
Interneurons
Locomotion
Membrane Potentials
Mice
Mice, Transgenic
Motor Neurons
N-Methylaspartate
Neurotransmitter Agents
Patch-Clamp Techniques
Serotonin
Spinal Cord
Spinal Nerve Roots
Time Factors
Transcription Factors
AbstractHb9 interneurons (Hb9 INs) are putative components of the mouse spinal locomotor central pattern generator (CPG) and candidates for the rhythm-generating kernel. Studies in slices and hemisected spinal cords showed that Hb9 INs display TTX-resistant membrane potential oscillations, suggesting a role in rhythm generation. To further investigate the roles of Hb9 INs in the locomotor CPG, we used two-photon calcium imaging in the in vitro isolated whole neonatal mouse spinal cord preparation to record the activity of Hb9 INs, which were subsequently stained for unambiguous genetic identification. We elicited fictive locomotion by transmitter application or by electrically stimulating the caudal tip of the spinal cord. Although most Hb9 INs were rhythmically active during fictive locomotion, their activity was sparse and they failed to fire with each cycle of the episode. If Hb9 INs are the principal pacemakers of the CPG in the hemisegment in which they are located, they should direct the firing of motor neurons, with their activity preceding that of their ipsilateral segmental ventral roots. Instead, during each locomotor cycle, onset of Hb9 IN activity lagged behind the onset of the ipsilateral ventral root burst by a mean phase of 0.21 during electrical stimulation and 0.28 during transmitter application. Whole-cell recordings in intact and hemisected spinal cords confirmed the imaging results. Our data suggest that Hb9 INs participate in fictive locomotion, but the delayed onset of activity relative to ipsilateral motoneurons suggests that Hb9 INs are unlikely to be the sole intrasegmental rhythm-generating kernel of the CPG.
Languageeng
Pub Type(s)In Vitro
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
PubMed ID19759307
  
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