- Poster presentation
- Open Access
Modeling study of a Central Pattern Generator in the Melibe seaslug
© Jalil et al; licensee BioMed Central Ltd. 2012
- Published: 16 July 2012
- Central Pattern Generator
- Network Configuration
- Synaptic Conductance
- Excitatory Drive
- Intrinsic Symmetry
Behaving animals show correlated neuronal activities in their nervous system. These observations lead to the question, how are the specific patterns of activities generated and used to control behaviors? Central Pattern Generators (CPGs) are small networks of neurons that are experimentally identified as necessary for expressions of behaviors, and the core group capable of controlling various aspects of the behavior. Mechanistic understanding of CPG functions is under intense investigation . In this study, we investigate the role of network configurations of an experimentally based CPG for swimming behavior in the marine invertebrate Melibe leonine .
Repetitive nature of activity patterns of CPGs can be examined through the relative phase relations between bursting interneurons. Experimentally and computationally, such phase-lags are measured with respect to a reference neuron, thus allowing for an analysis of various activity patterns in a systematic way. For the Melibe CPG model under consideration, we consider four Hodgkin-Huxley type square-wave bursters, connected via fast non-delayed inhibitory synapses represented by fast threshold modulating function. Due to intrinsic symmetry, the network can be treated as two pairs of half center oscillators (HCOs). In a HCO both neurons reciprocally inhibit each other, leading to alternate, anti-phase bursting patterns, which can coexist with in-phase bursting when the HCO is inhibited externally [3, 4]. In the given model, one HCO inhibits the other one and gets a positive feedback in the form of excitatory drive. We will further enhance the CPG model by including additional interneurons to reflect physiological fine details observed in-vitro. The exploration of stable phase-locked states, perturbed externally by applied current pulses, allows us to suggest plausible mechanisms of the CPG and come up with predictions that may be verified by electrophysiological experiments.
The phase-locked pattern, observed in the experiment, is identified as an attractor in numerical simulations. We find that specific distributions of synaptic conductance shift the attractor so that it merges with a saddle corresponding to unstable phase-locked state. Investigation indicates that weak excitatory connections play no significant role in the generation of the pattern but may have stabilizing effect. Electrical coupling, which appears to be very weak and negligible in the physiological context, may play a critical role in altering the behavior of the network.
We conclude that the idiosyncratic phase-locking seen in the experimental setup is due to a specific network configuration of the CPG model where a driving HCO uni-directionally inhibits a nearly identical one, provided that coupling strengths stay rather weak. Future investigations will be focused on enhanced realistic CPG models with additional connections and participating interneurons.
We acknowledge Brain and Behavior Fellowship provided by Neuroscience Institute at Georgia State University; NSF DMS-1009591 funding including REU.
- Marder E, Calabrese RL: Principles of rhythmic motor pattern generation. Physiol Rev. 1996, 76: 687-717.PubMedGoogle Scholar
- Sakurai A, Newcomb JM, Lillvis JL, Katz PS: Different Roles for Homologous Interneurons in Species Exhibiting Similar Rhythmic Behaviors. Curr Biol. 2011, 21: 1036-1043. 10.1016/j.cub.2011.04.040.View ArticlePubMedGoogle Scholar
- Jalil S, Belykh I, Shilnikov A: Fast reciprocal inhibition can synchronize bursting neurons. Phys Rev E. 2010, 81: 045201-045204(R).View ArticleGoogle Scholar
- Belykh IV, Shilnikov AL: When weak inhibition synchronizes strongly desynchronizing networks of bursting neurons. Phys Rev Letters. 2008, 101: 078102-078105.View ArticleGoogle Scholar
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