The Construction of Movement with Behavior-Specific and Behavior-Independent Modules

Growing evidence suggests that different forms of complex motor acts are constructed through flexible combinations of a small number of modules in interneuronal networks. It remains to be established, however, whether a module simply controls groups of muscles and functions as a computational unit for use in multiple behaviors (behavior independent) or whether a module controls multiple salient features that define one behavior and is used primarily for that behavior (behavior specific). We used the Aplysia feeding motor network to examine the two proposals by studying the functions of identifiable interneurons. We identified three types of motor programs that resemble three types of behaviors that Aplysia produce: biting, swallowing, and rejection. Two ingestive programs (biting, swallowing) are defined by two movement parameters of the feeding apparatus (the radula): one is the same in both programs (phasing of radula closure motoneurons relative to radula protraction-retraction), whereas the other parameter (protraction duration) is different in the two programs. In each program, these two parameters were specified together by an individual neuron, but the neurons in each were different (B40 for biting, B30 for swallowing). These findings support the existence of behavior-specific modules. Furthermore, neuron B51 was found to mediate a phase that can be flexibly added on to both ingestive and egestive-rejection programs, suggesting that B51 may be a behavior-independent module. The functional interpretation of the role played by these modules is supported by the patterns of synaptic connectivity that they make. Thus, both behavior-specific and behavior-independent modules are used to construct complex behaviors.

[1]  F. Plum Handbook of Physiology. , 1960 .

[2]  N. A. Bernshteĭn The co-ordination and regulation of movements , 1967 .

[3]  G. J. Thomas The Co-ordination and Regulation of Movements , 1967 .

[4]  F. Marriott Practical problems in a method of cluster analysis. , 1971, Biometrics.

[5]  I. Kupfermann Feeding behavior in Aplysia: a simple system for the study of motivation. , 1974, Behavioral biology.

[6]  I Kupfermann,et al.  Motor control of buccal muscles in Aplysia. , 1978, Journal of neurophysiology.

[7]  S. Grillner Control of Locomotion in Bipeds, Tetrapods, and Fish , 1981 .

[8]  S. Grillner Neurobiological bases of rhythmic motor acts in vertebrates. , 1985, Science.

[9]  P. Stein,et al.  Three forms of the scratch reflex in the spinal turtle: movement analyses. , 1985, Journal of neurophysiology.

[10]  H. Chiel,et al.  Activity of an identified histaminergic neuron, and its possible role in arousal of feeding behavior in semi-intact Aplysia , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  W. Krzanowski,et al.  A Criterion for Determining the Number of Groups in a Data Set Using Sum-of-Squares Clustering , 1988 .

[12]  M. Kirk,et al.  Premotor neurons B51 and B52 in the buccal ganglia of Aplysia californica: synaptic connections, effects on ongoing motor rhythms, and peptide modulation. , 1990, Journal of neurophysiology.

[13]  K. R. Weiss,et al.  Differential firing patterns of the peptide-containing cholinergic motor neurons B15 and B16 during feeding behavior inAplysia , 1990, Brain Research.

[14]  V. Reggie Edgerton,et al.  Neurobiological basis of human locomotion , 1991 .

[15]  F A Mussa-Ivaldi,et al.  Computations underlying the execution of movement: a biological perspective. , 1991, Science.

[16]  I Kupfermann,et al.  Identification and characterization of cerebral-to-buccal interneurons implicated in the control of motor programs associated with feeding in Aplysia , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  V. Castellucci,et al.  Contribution of polysynaptic pathways in the mediation and plasticity of Aplysia gill and siphon withdrawal reflex: evidence for differential modulation , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  P. Stein,et al.  Activity of descending propriospinal axons in the turtle hindlimb enlargement during two forms of fictive scratching: broad tuning to regions of the body surface , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[19]  P. Church,et al.  Activity of multiple identified motor neurons recorded intracellularly during evoked feedinglike motor programs in Aplysia. , 1994, Journal of neurophysiology.

[20]  P. Stein,et al.  Bilateral control of hindlimb scratching in the spinal turtle: contralateral spinal circuitry contributes to the normal ipsilateral motor pattern of fictive rostral scratching , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  P. Katz Neurons, Networks, and Motor Behavior , 1996, Neuron.

[22]  I. Hurwitz,et al.  B64, a newly identified central pattern generator element producing a phase switch from protraction to retraction in buccal motor programs of Aplysia californica. , 1996, Journal of neurophysiology.

[23]  H. Chiel,et al.  Activity patterns of the B31/B32 pattern initiators innervating the I2 muscle of the buccal mass during normal feeding movements in Aplysia californica. , 1996, Journal of neurophysiology.

[24]  W. Kristan,et al.  The role of population coding in the control of movement , 1997 .

[25]  I. Hurwitz,et al.  Different roles of neurons B63 and B34 that are active during the protraction phase of buccal motor programs in Aplysia californica. , 1997, Journal of neurophysiology.

[26]  E. Cropper,et al.  Proprioceptive Input to Feeding Motor Programs inAplysia , 1998, The Journal of Neuroscience.

[27]  F. Lacquaniti,et al.  Motor patterns for human gait: backward versus forward locomotion. , 1998, Journal of neurophysiology.

[28]  D M Wolpert,et al.  Multiple paired forward and inverse models for motor control , 1998, Neural Networks.

[29]  E. Bizzi,et al.  The construction of movement by the spinal cord , 1999, Nature Neuroscience.

[30]  Ferdinando A Mussa-Ivaldi,et al.  Modular features of motor control and learning , 1999, Current Opinion in Neurobiology.

[31]  D. A. Baxter,et al.  In Vitro Analog of Operant Conditioning inAplysia. II. Modifications of the Functional Dynamics of an Identified Neuron Contribute to Motor Pattern Selection , 1999, The Journal of Neuroscience.

[32]  J. Hopfield,et al.  From molecular to modular cell biology , 1999, Nature.

[33]  W J Kargo,et al.  Rapid Correction of Aimed Movements by Summation of Force-Field Primitives , 2000, The Journal of Neuroscience.

[34]  Zoubin Ghahramani,et al.  Computational principles of movement neuroscience , 2000, Nature Neuroscience.

[35]  Miguel A. L. Nicolelis,et al.  Advances in neural population coding , 2001 .

[36]  J. Jing,et al.  Neural Mechanisms of Motor Program Switching inAplysia , 2001, The Journal of Neuroscience.

[37]  J. Jing,et al.  Interneuronal and peptidergic control of motor pattern switching in Aplysia. , 2002, Journal of neurophysiology.

[38]  P. Stein,et al.  Modular Organization of Turtle Spinal Interneurons during Normal and Deletion Fictive Rostral Scratching , 2002, The Journal of Neuroscience.

[39]  J. Jing,et al.  Interneuronal Basis of the Generation of Related but Distinct Motor Programs in Aplysia: Implications for Current Neuronal Models of Vertebrate Intralimb Coordination , 2002, The Journal of Neuroscience.

[40]  Emilio Bizzi,et al.  Coordination and localization in spinal motor systems , 2002, Brain Research Reviews.

[41]  K. R. Weiss,et al.  Fast synaptic connections from CBIs to pattern-generating neurons in Aplysia: initiation and modification of motor programs. , 2003, Journal of neurophysiology.

[42]  Emilio Bizzi,et al.  Combinations of muscle synergies in the construction of a natural motor behavior , 2003, Nature Neuroscience.

[43]  J. Jing,et al.  A newly identified buccal interneuron initiates and modulates feeding motor programs in aplysia. , 2003, Journal of neurophysiology.

[44]  Ji-Ho Park,et al.  Concerted GABAergic Actions of Aplysia Feeding Interneurons in Motor Program Specification , 2003, The Journal of Neuroscience.

[45]  H. Chiel,et al.  In vivo buccal nerve activity that distinguishes ingestion from rejection can be used to predict behavioral transitions in Aplysia , 1993, Journal of Comparative Physiology A.

[46]  H. Chiel,et al.  The timing of activity in motor neurons that produce radula movements distinguishes ingestion from rejection in Aplysia , 1993, Journal of Comparative Physiology A.