Many everyday rhythmic activities such as breathing, chewing, and locomoting, are programed in part by neuronal networks called central pattern generators (CPGs). Mechanistic analysis of CPGs has been especially fruitful in the CPGs of invertebrates, which have relatively few neurons and can therefore be precisely defined in terms of identified neurons and specific synaptic connections. CPG networks of invertebrates have become proxies for experimental and theoretical analyses of how brain networks reliably yet flexibly process sensory information or program motor output. Our detailed analyses of the leech heartbeat CPG continue to contribute substantially to the organizing principles by which we now understand network function. Theoretical studies and experimental analysis in different networks and species have shown that the intrinsic membrane properties of the neurons and the strengths of their synaptic connections show 2-5 fold animal-to-animal variability, yet networks still produce functional output. Nevertheless, there are clear examples - including from our own work - showing that individual variation in synaptic and intrinsic properties do have functional consequences that manifest in network performance or susceptibility to perturbation. These studies imply that to understand fundamentally a neuronal network, we must strive to gather complete data from individuals because networks from individuals, while functionally stereotyped, may have different mechanistic underpinnings at the level of membrane currents and synaptic connections with discernible functional consequences. In light of this variation, an ensemble modeling approach is necessary to generate and test hypotheses about living networks. In this approach, multiple model instances (with different parameters) generated by evolutionary algorithms or brute force parameter variation are used. A prerequisite for this approach is experimental studies that determine parameter variation in the living system across a variety of networks. Our experiments will integrate computational and neurophysiological approaches to elucidate basic mechanisms of network function and the impact of individual variation in network parameters. Moreover, we will use individual variation as an innovative tool to probe network function. The leech heartbeat CPG is analogous to spinal CPGs that produce coordinated rhythmic activity in motor neurons, and its relative simplicity and superb accessibility allow a level of cellular analysis not currently possible in spinal cord. We will analyze the impact of inter-individual variation in CPG input and motor neuron intrinsic properties on motor output and how movements reflect this variation. These studies will provide basic mechanistic insights into network function in individuals, which will be useful in the study of spinal and brain networks and can lead to therapies for spinal cord and brain injury and disorders affecting motor performance.

Public Health Relevance

The leech heartbeat CPG is analogous to spinal CPGs that produce coordinated rhythmic activity in motor neurons, and its relative simplicity and superb accessibility allow a level of cellular analysis not currently possible in spinal cord. We will analyze the impact of inter-individual variation in CPG input and motor neuron intrinsic properties on motor output and how movements reflect this variation. These studies will provide basic mechanistic insights into network function in individuals, which will be useful in the study of spinal and brain networks and can lead to therapies for spinal cord and brain injury and disorders affecting motor performance.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS085006-03
Application #
8895431
Study Section
Sensorimotor Integration Study Section (SMI)
Program Officer
Chen, Daofen
Project Start
2013-09-15
Project End
2016-07-31
Budget Start
2015-08-01
Budget End
2016-07-31
Support Year
3
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Emory University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Calabrese, Ronald L (2018) Inconvenient Truth to Principle of Neuroscience. Trends Neurosci 41:488-491
Wenning, Angela; Norris, Brian J; Günay, Cengiz et al. (2018) Output variability across animals and levels in a motor system. Elife 7:
Calabrese, Ronald L (2017) Neural Evolution: Homology in Neuronal Networks. Curr Biol 27:R718-R719
Doloc-Mihu, Anca; Calabrese, Ronald L (2016) Analysis of Family Structures Reveals Robustness or Sensitivity of Bursting Activity to Parameter Variations in a Half-Center Oscillator (HCO) Model. eNeuro 3:
Calabrese, Ronald L; Norris, Brian J; Wenning, Angela (2016) The neural control of heartbeat in invertebrates. Curr Opin Neurobiol 41:68-77
Kueh, Daniel; Barnett, William H; Cymbalyuk, Gennady S et al. (2016) Na(+)/K(+) pump interacts with the h-current to control bursting activity in central pattern generator neurons of leeches. Elife 5:
Calabrese, Ronald L (2015) In search of lost scent. Elife 4:
Wenning, Angela; Norris, Brian J; Doloc-Mihu, Anca et al. (2014) Variation in motor output and motor performance in a centrally generated motor pattern. J Neurophysiol 112:95-109
Doloc-Mihu, Anca; Calabrese, Ronald L (2014) Identifying crucial parameter correlations maintaining bursting activity. PLoS Comput Biol 10:e1003678
Sober, Samuel J; Calabrese, Ronald L (2014) Falling on deaf neurons. Elife 3:e02289

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