Monoaminergic control of cauda-equina-evoked locomotion in the neonatal mouse spinal cord.

Monoaminergic projections are among the first supraspinal inputs to innervate spinal networks. Little is known regarding the role of monoamines in modulating ongoing locomotor patterns evoked by endogenous release of neurotransmitter. Here we activate a locomotor-like rhythm by electrical stimulation of afferents and then test the modulatory effects of monoamines on the frequency, pattern, and quality of the rhythm. Stimulation of the cauda equina induced a rhythm consisting of left-right and ipsilateral alternation indicative of locomotor-like activity. First, we examined the effects of noradrenaline (NA), serotonin (5-HT), or dopamine (DA) at dose levels that did not elicit locomotor activity. Bath application of NA and DA resulted in a depression of the cauda-equina-evoked rhythm. Conversely, bath-applied 5-HT increased both the amplitude and cycle period of the evoked rhythm, an effect that was mimicked by the addition of 5-HT(2) agonists to the bath. Application of 5-HT(7) agonists disrupted the evoked rhythmic behavior. Next, we examined the effects of NA alpha(1) and alpha(2) agonists and found that the suppressive effects of NA on the rhythm could be reproduced by adding the alpha(2) agonist, clonidine, to the bath. In contrast, bath applying the alpha(1) agonist, phenylephrine, increased the amplitude and duration of the cycle period. Finally, the suppressive effects of DA were not replicated by the administration of D(1), D(2), or D(3) agonists although application of NA alpha(2) antagonists reversed the effects of DA. Application of D(1) agonists, increased the amplitude of the bursts but did not affect the cycle period. Our results indicate that monoamines can control the expression, pattern, and timing of cauda-equina-evoked locomotor patterns in developing mice.

[1]  J. Weil-Fugazza,et al.  Dorsal and ventral dopaminergic innervation of the spinal cord: Functional implications , 1993, Brain Research Bulletin.

[2]  G. Basura,et al.  Distribution of Serotonin 2A and 2C Receptor mRNA Expression in the Cervical Ventral Horn and Phrenic Motoneurons Following Spinal Cord Hemisection , 2001, Experimental Neurology.

[3]  Sujay K. Singh,et al.  Expression of 5-HT2A, 5-HT2B and 5-HT2C receptors in the mouse embryo , 2000, International Journal of Developmental Neuroscience.

[4]  P. Whelan,et al.  Modulation of locomotor activity by multiple 5-HT and dopaminergic receptor subtypes in the neonatal mouse spinal cord. , 2004, Journal of neurophysiology.

[5]  N. Dale,et al.  Experimentally derived model for the locomotor pattern generator in the Xenopus embryo. , 1995, The Journal of physiology.

[6]  John Guckenheimer,et al.  Overexpression of a Hyperpolarization-Activated Cation Current (Ih) Channel Gene Modifies the Firing Activity of Identified Motor Neurons in a Small Neural Network , 2003, The Journal of Neuroscience.

[7]  R. Brownstone,et al.  Mechanisms underlying the early phase of spike frequency adaptation in mouse spinal motoneurones , 2005, The Journal of physiology.

[8]  Ronald M Harris-Warrick,et al.  Intrinsic and Functional Differences among Commissural Interneurons during Fictive Locomotion and Serotonergic Modulation in the Neonatal Mouse , 2006, The Journal of Neuroscience.

[9]  X. Li,et al.  Persistent sodium currents and repetitive firing in motoneurons of the sacrocaudal spinal cord of adult rats. , 2006, Journal of neurophysiology.

[10]  R. Harris-Warrick,et al.  Dopamine modulation of transient potassium current evokes phase shifts in a central pattern generator network , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  J. Cazalets,et al.  Noradrenergic control of locomotor networks in the in vitro spinal cord of the neonatal rat , 2000, Brain Research.

[12]  L. Jordan,et al.  The role of serotonin in reflex modulation and locomotor rhythm production in the mammalian spinal cord , 2000, Brain Research Bulletin.

[13]  N. Kudo,et al.  N-Methyl-d,l-aspartate-induced locomotor activity in a spinal cord-indlimb muscles preparation of the newborn rat studied in vitro , 1987, Neuroscience Letters.

[14]  P. Branchereau,et al.  Ontogenic Changes of the Spinal GABAergic Cell Population Are Controlled by the Serotonin (5-HT) System: Implication of 5-HT1 Receptor Family , 2005, The Journal of Neuroscience.

[15]  L. Vinay,et al.  Serotonin refines the locomotor‐related alternations in the in vitro neonatal rat spinal cord , 2005, The European journal of neuroscience.

[16]  H. Koch,et al.  Role of persistent sodium current in bursting activity of mouse neocortical networks in vitro. , 2006, Journal of neurophysiology.

[17]  A. Privat,et al.  Direct evidence for the link between monoaminergic descending pathways and motor activity: II. A study with microdialysis probes implanted in the ventral horn of the spinal cord , 1998, Brain Research.

[18]  D. Stehouwer,et al.  L-DOPA-induced air-stepping in the preweanling rat: electromyographic and kinematic analyses. , 2000, Behavioral neuroscience.

[19]  A. Privat,et al.  Study of 5-HT release with a chronically implanted microdialysis probe in the ventral horn of the spinal cord of unrestrained rats during exercise on a treadmill , 1994, Journal of Neuroscience Methods.

[20]  Edouard Pearlstein,et al.  Development of posture and locomotion: an interplay of endogenously generated activities and neurotrophic actions by descending pathways , 2002, Brain Research Reviews.

[21]  A. Lundberg,et al.  The effect of DOPA on the spinal cord. 6. Half-centre organization of interneurones transmitting effects from the flexor reflex afferents. , 1967, Acta physiologica Scandinavica.

[22]  X. Wang,et al.  Descending inhibition in the neonate rat spinal cord is mediated by 5-hydroxytryptamine , 1993, Neuropharmacology.

[23]  T. Narahashi,et al.  Effects of the neuroprotective agent riluzole on the high voltage-activated calcium channels of rat dorsal root ganglion neurons. , 1997, The Journal of pharmacology and experimental therapeutics.

[24]  A Lev-Tov,et al.  Pattern generation in caudal-lumbar and sacrococcygeal segments of the neonatal rat spinal cord. , 2002, Journal of neurophysiology.

[25]  C. Heckman,et al.  Essential role of the persistent sodium current in spike initiation during slowly rising inputs in mouse spinal neurones , 2006, The Journal of physiology.

[26]  E. Callaway,et al.  V1 spinal neurons regulate the speed of vertebrate locomotor outputs , 2006, Nature.

[27]  Hui Li,et al.  Serotonin potentiation of glycine-activated whole-cell currents in the superficial laminae neurons of the rat spinal dorsal horn is mediated by protein kinase C , 2002, Brain Research Bulletin.

[28]  J. Feldman,et al.  Sodium and Calcium Current-Mediated Pacemaker Neurons and Respiratory Rhythm Generation , 2005, The Journal of Neuroscience.

[29]  Julian F R Paton,et al.  Respiratory rhythm generation during gasping depends on persistent sodium current , 2006, Nature Neuroscience.

[30]  James N. Davis,et al.  Postnatal development of brain alpha1-adrenergic receptors: In vitro autoradiography with [125i]HEAT in normal rats and rats treated with alpha-difluoromethylornithine, a specific, irreversible inhibitor of ornithine decarboxylase , 1985, Neuroscience.

[31]  M. Geffard,et al.  Spinal dopaminergic system of the rat: light and electron microscopic study using an antiserum against dopamine, with particular emphasis on synaptic incidence , 1992, Brain Research.

[32]  S. Grillner,et al.  Calcium-dependent potassium channels play a critical role for burst termination in the locomotor network in lamprey. , 1994, Journal of neurophysiology.

[33]  P. Branchereau,et al.  Descending 5-Hydroxytryptamine Raphe Inputs Repress the Expression of Serotonergic Neurons and Slow the Maturation of Inhibitory Systems in Mouse Embryonic Spinal Cord , 2002, The Journal of Neuroscience.

[34]  R. Harris-Warrick Voltage-sensitive ion channels in rhythmic motor systems , 2002, Current Opinion in Neurobiology.

[35]  T. Jessell,et al.  Conditional Rhythmicity of Ventral Spinal Interneurons Defined by Expression of the Hb9 Homeodomain Protein , 2005, The Journal of Neuroscience.

[36]  R. Harris-Warrick,et al.  Modulation of neural networks for behavior. , 1991, Annual review of neuroscience.

[37]  Ole Kiehn,et al.  Role of EphA4 and EphrinB3 in Local Neuronal Circuits That Control Walking , 2003, Science.

[38]  A Lev-Tov,et al.  Neural pathways between sacrocaudal afferents and lumbar pattern generators in neonatal rats. , 2003, Journal of neurophysiology.

[39]  P. Whelan,et al.  Deciphering the organization and modulation of spinal locomotor central pattern generators , 2006, Journal of Experimental Biology.

[40]  W. Crill,et al.  Persistent sodium current in mammalian central neurons. , 1996, Annual review of physiology.

[41]  S. Hochman,et al.  Pharmacological characterization of serotonin receptor subtypes modulating primary afferent input to deep dorsal horn neurons in the neonatal rat , 2001, British journal of pharmacology.

[42]  J. Holstege,et al.  Distribution of dopamine immunoreactivity in the rat, cat, and monkey spinal cord , 1996, The Journal of comparative neurology.

[43]  B. Jacobs,et al.  5-HT and motor control: a hypothesis , 1993, Trends in Neurosciences.

[44]  A Lev-Tov,et al.  Alpha-1 adrenoceptor agonists generate a "fast" NMDA receptor-independent motor rhythm in the neonatal rat spinal cord. , 2004, Journal of neurophysiology.

[45]  D. Vergé,et al.  The 5‐HT2A receptor is widely distributed in the rat spinal cord and mainly localized at the plasma membrane of postsynaptic neurons , 2004, The Journal of comparative neurology.

[46]  F. Clarac,et al.  Activation of the central pattern generators for locomotion by serotonin and excitatory amino acids in neonatal rat. , 1992, The Journal of physiology.

[47]  Michael J. O'Donovan,et al.  Properties of rhythmic activity generated by the isolated spinal cord of the neonatal mouse. , 2000, Journal of neurophysiology.

[48]  M. Geffard,et al.  Pre- and postnatal development of noradrenergic projections to the rat spinal cord: an immunocytochemical study. , 1992, Brain research. Developmental brain research.

[49]  R. Harris-Warrick,et al.  Distributed Effects of Dopamine Modulation in the Crustacean Pyloric Network a , 1998, Annals of the New York Academy of Sciences.

[50]  Masatoshi Tanaka,et al.  Existence of new dopaminergic terminal plexus in the rat spinal cord: assessment by immunohistochemistry using anti-dopamine serum , 1988, Neuroscience Letters.

[51]  K. Sung,et al.  Inhibition of the cloned delayed rectifier K+ channels, Kv1.5 and Kv3.1, by riluzole , 2005, Neuroscience.

[52]  C. Heckman,et al.  Increased persistent Na+ current and its effect on excitability in motoneurones cultured from mutant SOD1 mice , 2005, The Journal of physiology.

[53]  T. Jessell,et al.  Genetic Identification of Spinal Interneurons that Coordinate Left-Right Locomotor Activity Necessary for Walking Movements , 2004, Neuron.

[54]  D. McCrea,et al.  Modelling spinal circuitry involved in locomotor pattern generation: insights from deletions during fictive locomotion , 2006, The Journal of physiology.

[55]  I. Delvolvé,et al.  The motor output and behavior produced by rhythmogenic sacrocaudal networks in spinal cords of neonatal rats. , 2001, Journal of neurophysiology.

[56]  Consuelo Morgado-Valle,et al.  Respiratory Rhythm An Emergent Network Property? , 2002, Neuron.

[57]  G. Bernardi,et al.  Kainate‐induced currents in rat cortical neurons in culture are modulated by riluzole , 2002, Synapse.

[58]  E. Jankowska,et al.  Modulatory Effects of α1-, α2-, and β-Receptor Agonists on Feline Spinal Interneurons with Monosynaptic Input from Group I Muscle Afferents , 2003, The Journal of Neuroscience.

[59]  M. Geffard,et al.  Evidence for nonsynaptic serotonergic and noradrenergic innervation of the rat dorsal horn and possible involvement of neuron-glia interactions , 1993, Neuroscience.

[60]  I. Delvolvé,et al.  Pattern generation in non-limb moving segments of the mammalian spinal cord , 2000, Brain Research Bulletin.

[61]  A. Patel,et al.  The neuroprotective agent riluzole activates the two P domain K(+) channels TREK-1 and TRAAK. , 2000, Molecular pharmacology.

[62]  S. Barasi,et al.  RESPONSES OF MOTONEURONES TO ELECTROPHORETICALLY APPLIED DOPAMINE , 1977, British journal of pharmacology.

[63]  Linying Wu,et al.  Locomotor-like rhythms in a genetically distinct cluster of interneurons in the mammalian spinal cord. , 2005, Journal of neurophysiology.

[64]  A. Privat,et al.  Direct evidence for the link between monoaminergic descending pathways and motor activity. I. A study with microdialysis probes implanted in the ventral funiculus of the spinal cord , 1995, Brain Research.

[65]  Michael J. O'Donovan,et al.  Locomotor-like activity generated by the neonatal mouse spinal cord , 2002, Brain Research Reviews.

[66]  S Grillner,et al.  Roles of high-voltage-activated calcium channel subtypes in a vertebrate spinal locomotor network. , 2000, Journal of neurophysiology.

[67]  E. Jankowska,et al.  The actions of monoamines and distribution of noradrenergic and serotoninergic contacts on different subpopulations of commissural interneurons in the cat spinal cord , 2004, The European journal of neuroscience.

[68]  H. Hatt,et al.  Dopamine enhances glutamate-activated currents in spinal motoneurons , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[69]  L. Jordan,et al.  Propriospinal neurons involved in the control of locomotion: potential targets for repair strategies? , 2002, Progress in brain research.

[70]  Anders Lansner,et al.  Computer simulation of the segmental neural network generating locomotion in lamprey by using populations of network interneurons , 2004, Biological Cybernetics.

[71]  G. Bernardi,et al.  Riluzole interacts with voltage-activated sodium and potassium currents in cultured rat cortical neurons , 1998, Neuroscience.

[72]  J. Stamford Descending control of pain. , 1995, British journal of anaesthesia.

[73]  M. Savasta,et al.  Autoradiographic distribution of the D1 agonist [3H]SKF 38393, in the rat brain and spinal cord. Comparison with the distribution of D2 dopamine receptors , 1986, Neuroscience.

[74]  N. Mellen,et al.  Neuromodulation of the locomotor network by dopamine in the isolated spinal cord of newborn rat , 2004, The European journal of neuroscience.

[75]  Ole Kiehn,et al.  Firing Properties of Identified Interneuron Populations in the Mammalian Hindlimb Central Pattern Generator , 2002, The Journal of Neuroscience.

[76]  T. Hökfelt,et al.  Distribution of alpha2-adrenoceptor mRNAs in the rat lumbar spinal cord in normal and axotomized rats. , 1999, Neuroreport.

[77]  A. Urbani,et al.  Riluzole inhibits the persistent sodium current in mammalian CNS neurons , 2000, The European journal of neuroscience.

[78]  Ronald M Harris-Warrick,et al.  Serotonin modulates the properties of ascending commissural interneurons in the neonatal mouse spinal cord. , 2006, Journal of neurophysiology.

[79]  J. J. Couey,et al.  Modulation of recombinant and native neuronal SK channels by the neuroprotective drug riluzole. , 2002, European journal of pharmacology.

[80]  L M Jordan,et al.  Cholinergic and serotonergic excitation of ascending commissural neurons in the thoraco-lumbar spinal cord of the neonatal mouse. , 2006, Journal of neurophysiology.

[81]  R. Wightman,et al.  Catecholamine release and uptake in the mouse prefrontal cortex , 2001, Journal of neurochemistry.

[82]  O. Kiehn,et al.  EphA4 defines a class of excitatory locomotor-related interneurons. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[83]  O Kiehn,et al.  Distribution of Networks Generating and Coordinating Locomotor Activity in the Neonatal Rat Spinal Cord In Vitro: A Lesion Study , 1996, The Journal of Neuroscience.

[84]  A. Lundberg,et al.  The effect of DOPA on the spinal cord. 5. Reciprocal organization of pathways transmitting excitatory action to alpha motoneurones of flexors and extensors. , 1967, Acta physiologica Scandinavica.

[85]  John Simmers,et al.  Propriospinal Circuitry Underlying Interlimb Coordination in Mammalian Quadrupedal Locomotion , 2005, The Journal of Neuroscience.

[86]  E Jankowska,et al.  Spinal interneurones; how can studies in animals contribute to the understanding of spinal interneuronal systems in man? , 2002, Brain Research Reviews.

[87]  E. Izhikevich,et al.  Persistent sodium currents in mesencephalic v neurons participate in burst generation and control of membrane excitability. , 2005, Journal of neurophysiology.

[88]  Elzbieta Jankowska,et al.  Networks of inhibitory and excitatory commissural interneurons mediating crossed reticulospinal actions , 2003, The European journal of neuroscience.

[89]  F. Clarac,et al.  Localization and organization of the central pattern generator for hindlimb locomotion in newborn rat , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[90]  F. Clarac,et al.  Reversible Disorganization of the Locomotor Pattern after Neonatal Spinal Cord Transection in the Rat , 2003, The Journal of Neuroscience.

[91]  B. Bean,et al.  Ionic Mechanisms of Burst Firing in Dissociated Purkinje Neurons , 2003, The Journal of Neuroscience.

[92]  E. Jankowska,et al.  Functional differentiation and organization of feline midlumbar commissural interneurones , 2005, The Journal of physiology.

[93]  T. Hökfelt,et al.  Differential distribution of alpha2A and alpha2C adrenergic receptor immunoreactivity in the rat spinal cord. , 1998, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[94]  O. Kiehn,et al.  Distribution of Central Pattern Generators for Rhythmic Motor Outputs in the Spinal Cord of Limbed Vertebrates a , 1998, Annals of the New York Academy of Sciences.

[95]  J. Wu,et al.  Is 5-hydroxytryptamine mediating descending inhibition in the neonatal rat spinal cord through different receptor subtypes? , 1993, European Journal of Pharmacology.

[96]  R. Brownstone,et al.  Development of L‐type calcium channels and a nifedipine‐sensitive motor activity in the postnatal mouse spinal cord , 1999, The European journal of neuroscience.

[97]  D. McCrea,et al.  Deletions of rhythmic motoneuron activity during fictive locomotion and scratch provide clues to the organization of the mammalian central pattern generator. , 2005, Journal of neurophysiology.

[98]  O. Kiehn,et al.  Functional Identification of Interneurons Responsible for Left-Right Coordination of Hindlimbs in Mammals , 2003, Neuron.

[99]  R. Miledi,et al.  Distribution of serotonin 2A, 2C and 3 receptor mRNA in spinal cord and medulla oblongata. , 2001, Brain research. Molecular brain research.

[100]  K. Sillar,et al.  Development and Aminergic Neuromodulation of a Spinal Locomotor Network Controlling Swimming in Xenopus Larvae a , 1998, Annals of the New York Academy of Sciences.

[101]  Jürg Streit,et al.  INaP underlies intrinsic spiking and rhythm generation in networks of cultured rat spinal cord neurons , 2004, The European journal of neuroscience.

[102]  S. Fleetwood-Walker,et al.  Antinociceptive actions of descending dopaminergic tracts on cat and rat dorsal horn somatosensory neurones. , 1988, The Journal of physiology.

[103]  E. Marder,et al.  Principles of rhythmic motor pattern generation. , 1996, Physiological reviews.

[104]  S. Hochman,et al.  Conversion of the Modulatory Actions of Dopamine on Spinal Reflexes from Depression to Facilitation in D3 Receptor Knock-Out Mice , 2004, The Journal of Neuroscience.

[105]  K. Sillar,et al.  Effects of noradrenaline on locomotor rhythm-generating networks in the isolated neonatal rat spinal cord. , 1999, Journal of neurophysiology.

[106]  O Kiehn,et al.  Characterization of commissural interneurons in the lumbar region of the neonatal rat spinal cord , 1999, The Journal of comparative neurology.

[107]  B. Schmidt,et al.  Regional distribution of the locomotor pattern-generating network in the neonatal rat spinal cord. , 1997, Journal of neurophysiology.

[108]  I. Delvolvé,et al.  Sacrocaudal afferents induce rhythmic efferent bursting in isolated spinal cords of neonatal rats. , 2000, Journal of neurophysiology.

[109]  Ole Kiehn,et al.  Activity of Renshaw Cells during Locomotor-Like Rhythmic Activity in the Isolated Spinal Cord of Neonatal Mice , 2006, The Journal of Neuroscience.

[110]  E. Jankowska Spinal interneuronal systems: identification, multifunctional character and reconfigurations in mammals , 2001, The Journal of physiology.

[111]  J. Balthazart,et al.  Dopamine Activates Noradrenergic Receptors in the Preoptic Area , 2002, The Journal of Neuroscience.

[112]  H. Suzuki,et al.  Serotonergic fibers induce a long-lasting inhibition of monosynaptic reflex in the neonatal rat spinal cord , 1992, Neuroscience.

[113]  P. Branchereau,et al.  Ontogeny of descending serotonergic innervation and evidence for intraspinal 5-HT neurons in the mouse spinal cord. , 2002, Brain research. Developmental brain research.

[114]  L. Jordan,et al.  Stimulation of the parapyramidal region of the neonatal rat brain stem produces locomotor-like activity involving spinal 5-HT7 and 5-HT2A receptors. , 2005, Journal of neurophysiology.

[115]  A. El Manira,et al.  Characterization of a high-voltage-activated IA current with a role in spike timing and locomotor pattern generation , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[116]  T. Hökfelt,et al.  Differential Distribution of α2A and α2C Adrenergic Receptor Immunoreactivity in the Rat Spinal Cord , 1998, The Journal of Neuroscience.

[117]  C. Zona,et al.  Modulation of AMPA receptors in spinal motor neurons by the neuroprotective agent riluzole , 2004, Journal of neuroscience research.

[118]  T. Hökfelt,et al.  Differential Distribution of a 2 A and a 2 C Adrenergic Receptor Immunoreactivity in the Rat Spinal Cord , 1998 .

[119]  Effects of flufenamic acid on fictive locomotion, plateau potentials, calcium channels and NMDA receptors in the lamprey spinal cord , 2006, Neuropharmacology.

[120]  A. Berkowitz,et al.  Activity of descending propriospinal axons in the turtle hindlimb enlargement during two forms of fictive scratching: phase analyses , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[121]  D. Vergé,et al.  Pre‐ and postsynaptic localization of the 5‐HT7 receptor in rat dorsal spinal cord: Immunocytochemical evidence , 2005, The Journal of comparative neurology.