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Author Notes:

Cengiz Günay : cgunay@ggc.edu

C.G., D.G.L., and R.L.C. designed research; C.G. performed research; C.G. and A.D.-M. contributed unpublished reagents/analytic tools; C.G. analyzed data; C.G., A.D.-M., D.G.L., and R.L.C. wrote the paper.

We thank Dr. Angela Wenning and Dr. Brian J. Norris for their insight into the fine details of heart neurons in Hirudo sp., support, immense biological data, and friendship through the years.

The authors declare no competing financial interests.

Subject:

Research Funding:

This work was supported by National Institutes of Health National Institute of Neurological Disorders and Stroke Grants 1 R01 NS085006, R01 NS024072, and R56 NS024072.

Keywords:

  • animal to animal variability
  • hirudo medicinalis
  • intrinsic membrane properties
  • motor networks
  • neuron simulation
  • synaptic variability

Journal Title:

eNeuro

Volume:

Volume 6, Number 4

Publisher:

Type of Work:

Article | Final Publisher PDF

Abstract:

Identified neurons and the networks they compose produce stereotypical, albeit individually unique, activity across members of a species. We propose, for a motor circuit driven by a central pattern generator (CPG), that the uniqueness derives mainly from differences in synaptic strength rather than from differences in intrinsic membrane conductances. We studied a dataset of recordings from six leech (Hirudo sp.) heartbeat control networks, containing complete spiking activity patterns from inhibitory premotor interneurons, motor output spike patterns, and synaptic strength patterns to investigate the source of uniqueness. We used a conductance-based multicompartmental motor neuron model to construct a bilateral motor circuit model, and controlled it by playing recorded input spike trains from premotor interneurons to generate output inhibitory synaptic patterns similar to experimental measurements. By generating different synaptic conductance parameter sets of this circuit model, we found that relative premotor synaptic strengths impinging onto motor neurons must be different across individuals to produce animal-specific output burst phasing. Obtaining unique outputs from each individual’s circuit model did not require different intrinsic ionic conductance parameters. Furthermore, changing intrinsic conductances failed to compensate for modified synaptic strength patterns. Thus, the pattern of synaptic strengths of motor neuron inputs is critical for the phasing of this motor circuit and can explain individual differences. When intrinsic conductances were allowed to vary, they exhibited the same conductance correlations across individuals, suggesting a motor neuron “type” required for proper network function. Our results are general and may translate to other systems and neuronal networks that control output phasing.

Copyright information:

© 2019 Günay et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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