Functional Recovery after Lesion of a Central Pattern Generator

In cases of neuronal injury when regeneration is restricted, functional recovery can occur through reorganization of the remaining neural circuitry. We found an example of such recovery in the central pattern generator (CPG) for the escape swim of the mollusc Tritonia diomedea. The CPG neurons are bilaterally represented and each neuron projects an axon through one of two pedal commissures. Cutting the posterior pedal commissure [pedal nerve 6 (PdN6)] in the animal or in the isolated brain caused a deficit in the swim behavior and in the fictive motor pattern, respectively, each of which recovered over the course of 20 h. Locally blocking spiking activity in PdN6 with sodium-free saline and/or tetrodotoxin disrupted the motor pattern in a reversible manner. Maintained blockade of PdN6 led to a functional recovery of the swim motor pattern similar to that observed in response to cutting the commissure. Among the CPG neurons, cerebral neuron 2 (C2) makes functional connection onto the ventral swim interneuron-B (VSI) in both pedal ganglia. Cutting or blocking PdN6 eliminated C2-evoked excitation of VSI in the pedal ganglion distal to the lesion. Associated with the recovery of the swim motor pattern, the synaptic action of C2 onto VSI in the proximal pedal ganglion changed from being predominantly inhibitory to being predominantly excitatory. These results show that the Tritonia swim CPG undergoes adaptive plasticity in response to the loss of critical synaptic connections; reversal of synaptic action in the CPG may be at least partially responsible for this functional recovery.

[1]  Tian,et al.  Swim Initiation Neurons in Tritonia diomedea , 2002 .

[2]  G. Davis Homeostatic control of neural activity: from phenomenology to molecular design. , 2006, Annual review of neuroscience.

[3]  V. Edgerton,et al.  Plasticity of the spinal neural circuitry after injury. , 2004, Annual review of neuroscience.

[4]  S. Rossignol Plasticity of connections underlying locomotor recovery after central and/or peripheral lesions in the adult mammals , 2006, Philosophical Transactions of the Royal Society B: Biological Sciences.

[5]  M. Kirk,et al.  Axonal regeneration in the central nervous system of Aplysia californica determined by anterograde transport of biocytin , 1999, The Journal of comparative neurology.

[6]  Evan S Hill,et al.  Role of membrane potential in calcium signaling during rhythmic bursting in tritonia swim interneurons. , 2007, Journal of neurophysiology.

[7]  R. Calabrese,et al.  Multiple sites of spike initiation in a single dendritic system. , 1974, Brain research.

[8]  Giorgio A Ascoli,et al.  A new bursting model of CA3 pyramidal cell physiology suggests multiple locations for spike initiation. , 2002, Bio Systems.

[9]  Juha Voipio,et al.  Cation–chloride co-transporters in neuronal communication, development and trauma , 2003, Trends in Neurosciences.

[10]  E. Marder,et al.  Variability, compensation and homeostasis in neuron and network function , 2006, Nature Reviews Neuroscience.

[11]  X. Navarro,et al.  Neural plasticity after peripheral nerve injury and regeneration , 2007, Progress in Neurobiology.

[12]  P A Getting,et al.  Motor organization of Tritonia swimming. II. Synaptic drive to flexion neurons from premotor interneurons. , 1982, Journal of neurophysiology.

[13]  J. Simmers,et al.  Neuromodulatory Inputs Maintain Expression of a Lobster Motor Pattern-Generating Network in a Modulation-Dependent State: Evidence from Long-Term Decentralization In Vitro , 1998, The Journal of Neuroscience.

[14]  C. Sahley,et al.  Multiple sites of action potential initiation increase neuronal firing rate. , 2001, Journal of neurophysiology.

[15]  P. Katz,et al.  Intrinsic neuromodulation in the Tritonia swim CPG: the serotonergic dorsal swim interneurons act presynaptically to enhance transmitter release from interneuron C2 , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  Pedal neuron 3 serves a significant role in effecting turning during crawling by the marine slug Tritonia diomedea (Bergh) , 2005, Journal of Comparative Physiology A.

[17]  L. Vinay,et al.  Inhibitory postsynaptic potentials in lumbar motoneurons remain depolarizing after neonatal spinal cord transection in the rat. , 2006, Journal of neurophysiology.

[18]  Jorge Golowasch,et al.  Ionic mechanism underlying recovery of rhythmic activity in adult isolated neurons. , 2006, Journal of neurophysiology.

[19]  J. Barthe,et al.  Locomotor recovery in the chronic spinal rat: effects of long‐term treatment with a 5‐HT2 agonist , 2002, The European journal of neuroscience.

[20]  G. Hoyle,et al.  The neuronal basis of behavior in Tritonia. I. Functional organization of the central nervous system. , 1973, Journal of neurobiology.

[21]  1-Phenoxy-2-propanol is a useful anaesthetic for gastropods used in neurophysiology , 2009, Journal of Neuroscience Methods.

[22]  D. Zecevic,et al.  Multiple spike-initiation zones in single neurons revealed by voltage-sensitive dyes , 1996, Nature.

[23]  E. Marder,et al.  Episodic bouts of activity accompany recovery of rhythmic output by a neuromodulator- and activity-deprived adult neural network. , 2003, Journal of neurophysiology.

[24]  S. Rossignol,et al.  Re-expression of locomotor function after partial spinal cord injury. , 2009, Physiology.

[25]  Paul S. Katz,et al.  Tritonia swim network , 2009, Scholarpedia.

[26]  P. A. Getting Mechanisms of pattern generation underlying swimming in Tritonia. I. Neuronal network formed by monosynaptic connections. , 1981, Journal of Neurophysiology.

[27]  K. Westberg,et al.  Do muscle-spindle afferent act as interneurons during mastication? , 1995, Trends in Neurosciences.

[28]  Michael J. O'Donovan,et al.  Dual personality of GABA/glycine-mediated depolarizations in immature spinal cord , 2007, Proceedings of the National Academy of Sciences.

[29]  Steven C. Cramer Repairing the human brain after stroke: I. Mechanisms of spontaneous recovery , 2008, Annals of neurology.

[30]  S. Rossignol Locomotion and its recovery after spinal injury , 2000, Current Opinion in Neurobiology.

[31]  A. Sik,et al.  Transition to seizures in the isolated immature mouse hippocampus: a switch from dominant phasic inhibition to dominant phasic excitation , 2008, The Journal of physiology.

[32]  P. R. Lennard,et al.  Central pattern generator mediating swimming in Tritonia. I. Identification and synaptic interactions. , 1980, Journal of neurophysiology.

[33]  V R Edgerton,et al.  Plasticity of functional connectivity in the adult spinal cord , 2006, Philosophical Transactions of the Royal Society B: Biological Sciences.

[34]  Bo Yang,et al.  A rapid switch in sympathetic neurotransmitter release properties mediated by the p75 receptor , 2002, Nature Neuroscience.

[35]  J. Golowasch,et al.  Activity and neuromodulatory input contribute to the recovery of rhythmic output after decentralization in a central pattern generator. , 2009, Journal of neurophysiology.

[36]  P. Katz,et al.  Comparative mapping of serotonin‐immunoreactive neurons in the central nervous systems of nudibranch molluscs , 2006, The Journal of comparative neurology.

[37]  S. Rossignol,et al.  Recovery of locomotion after chronic spinalization in the adult cat , 1987, Brain Research.

[38]  Serge Rossignol,et al.  Prominent Role of the Spinal Central Pattern Generator in the Recovery of Locomotion after Partial Spinal Cord Injuries , 2008, The Journal of Neuroscience.

[39]  E. Marder,et al.  Multiple axonal spike initiation zones in a motor neuron: serotonin activation , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[40]  F. P. Haugen,et al.  Functional Organization of the Central Nervous System , 1954, Neurology.

[41]  P. A. Getting Mechanisms of pattern generation underlying swimming in Tritonia. III. Intrinsic and synaptic mechanisms for delayed excitation. , 1983, Journal of neurophysiology.

[42]  Michael J. O'Donovan,et al.  Tapping into spinal circuits to restore motor function , 1999, Brain Research Reviews.

[43]  Y. Sauve,et al.  Recovery of function in spinalized, neonatal rats , 1991, Brain Research Bulletin.

[44]  T. Wieloch,et al.  Mechanisms of neural plasticity following brain injury , 2006, Current Opinion in Neurobiology.

[45]  W N Frost,et al.  Single neuron control over a complex motor program. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[46]  L. Vinay,et al.  Plasticity of spinal cord locomotor networks and contribution of cation–chloride cotransporters , 2008, Brain Research Reviews.

[47]  John Simmers,et al.  Long-term neuromodulatory regulation of a motor pattern-generating network: maintenance of synaptic efficacy and oscillatory properties. , 2002, Journal of neurophysiology.

[48]  G. Turrigiano Homeostatic plasticity in neuronal networks: the more things change, the more they stay the same , 1999, Trends in Neurosciences.

[49]  A. Cohen,et al.  Functional regeneration following spinal transection demonstrated in the isolated spinal cord of the larval sea lamprey. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[50]  Robert J Calin-Jageman,et al.  Parameter space analysis suggests multi-site plasticity contributes to motor pattern initiation in Tritonia. , 2007, Journal of neurophysiology.

[51]  S. Rossignol,et al.  Antidromic discharges in dorsal roots of decerebrate cats I. Studies at rest and during fictive locomotion , 1999, Brain Research.

[52]  John D. Slonimsky,et al.  BDNF and CNTF regulate cholinergic properties of sympathetic neurons through independent mechanisms , 2003, Molecular and Cellular Neuroscience.

[53]  Ronald L Calabrese,et al.  Phase relationships between segmentally organized oscillators in the leech heartbeat pattern generating network. , 2002, Journal of neurophysiology.

[54]  P. Katz,et al.  Spike Timing-Dependent Serotonergic Neuromodulation of Synaptic Strength Intrinsic to a Central Pattern Generator Circuit , 2003, The Journal of Neuroscience.

[55]  B. Tedeschi,et al.  Peripheral nerve regeneration. , 1991, Neurosurgery clinics of North America.

[56]  R. Nudo Mechanisms for recovery of motor function following cortical damage , 2006, Current Opinion in Neurobiology.

[57]  K. Lamsa,et al.  Use-dependent shift from inhibitory to excitatory GABAA receptor action in SP-O interneurons in the rat hippocampal CA3 area. , 2003, Journal of neurophysiology.

[58]  Jing Yang,et al.  Spinal cord injury‐induced attenuation of GABAergic inhibition in spinal dorsal horn circuits is associated with down‐regulation of the chloride transporter KCC2 in rat , 2008, The Journal of physiology.