Light-Induced Rescue of Breathing after Spinal Cord Injury

Paralysis is a major consequence of spinal cord injury (SCI). After cervical SCI, respiratory deficits can result through interruption of descending presynaptic inputs to respiratory motor neurons in the spinal cord. Expression of channelrhodopsin-2 (ChR2) and photostimulation in neurons affects neuronal excitability and produces action potentials without any kind of presynaptic inputs. We hypothesized that after transducing spinal neurons in and around the phrenic motor pool to express ChR2, photostimulation would restore respiratory motor function in cervical SCI adult animals. Here we show that light activation of ChR2-expressing animals was sufficient to bring about recovery of respiratory diaphragmatic motor activity. Furthermore, robust rhythmic activity persisted long after photostimulation had ceased. This recovery was accomplished through a form of respiratory plasticity and spinal adaptation which is NMDA receptor dependent. These data suggest a novel, minimally invasive therapeutic avenue to exercise denervated circuitry and/or restore motor function after SCI.

[1]  W. Porter The Path of the Respiratory Impulse from the Bulb to the Phrenic Nuclei , 1895, The Journal of physiology.

[2]  R. Skinner,et al.  Cells of origin of long descending propriospinal fibers connecting the spinal enlargements in cat and monkey determined by horseradish peroxidase and electrophysiological techniques , 1979, The Journal of comparative neurology.

[3]  A. Aguayo,et al.  Influences of the glial environment on the elongation of axons after injury: transplantation studies in adult rodents. , 1981, The Journal of experimental biology.

[4]  W. Willis,et al.  An estimate of the ratio of propriospinal to long tract neurons in the sacral spinal cord of the rat , 1984, Neuroscience Letters.

[5]  S. Rossignol,et al.  Electromyographic study of lumbar back muscles during locomotion in acute high decerebrate and in low spinal cats , 1984, Brain Research.

[6]  M. Schwab,et al.  Dissociated neurons regenerate into sciatic but not optic nerve explants in culture irrespective of neurotrophic factors , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[7]  D. Menétrey,et al.  Propriospinal fibers reaching the lumbar enlargement in the rat , 1985, Neuroscience Letters.

[8]  R. Coggeshall,et al.  Primary afferent and propriospinal fibers in the rat dorsal and dorsolateral funiculi , 1987, The Journal of comparative neurology.

[9]  A. Aguayo,et al.  Regeneration of axons from the central nervous system of adult rats. , 1987, Progress in brain research.

[10]  P. Caroni,et al.  Antibody against myelin associated inhibitor of neurite growth neutralizes nonpermissive substrate properties of CNS white matter , 1988, Neuron.

[11]  J. C. Smith,et al.  Pre-Bötzinger complex: a brainstem region that may generate respiratory rhythm in mammals. , 1991, Science.

[12]  S. Nakanishi,et al.  Molecular cloning and characterization of the rat NMDA receptor , 1991, Nature.

[13]  S. Grillner,et al.  Neural mechanisms of intersegmental coordination in lamprey: local excitability changes modify the phase coupling along the spinal cord. , 1992, Journal of neurophysiology.

[14]  J. Nadler,et al.  Kindling enhances sensitivity of CA3 hippocampal pyramidal cells to NMDA , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  J. Nadler,et al.  Kindling induces the long-lasting expression of a novel population of NMDA receptors in hippocampal region CA3 , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  S. T. Buckland,et al.  An Introduction to the Bootstrap. , 1994 .

[17]  J. Isaac,et al.  Evidence for silent synapses: Implications for the expression of LTP , 1995, Neuron.

[18]  T. Kuner,et al.  The NMDA receptor channel: molecular design of a coincidence detector. , 1995, Recent progress in hormone research.

[19]  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.

[20]  D. Basso,et al.  A sensitive and reliable locomotor rating scale for open field testing in rats. , 1995, Journal of neurotrauma.

[21]  Sheila M. Thomas,et al.  Calcium influx induces neurite growth through a Src-Ras signaling cassette , 1995, Neuron.

[22]  Michael S. Beattie,et al.  Graded Histological and Locomotor Outcomes after Spinal Cord Contusion Using the NYU Weight-Drop Device versus Transection , 1996, Experimental Neurology.

[23]  Yihai Cao,et al.  Spinal Cord Repair in Adult Paraplegic Rats: Partial Restoration of Hind Limb Function , 1996, Science.

[24]  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.

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

[26]  A. Prochazka,et al.  Phasic activity in the human erector spinae during repetitive hand movements , 1997, The Journal of physiology.

[27]  Activity of thoracic and lumbar epaxial extensors during postural responses in the cat , 1998, Experimental Brain Research.

[28]  G W Plant,et al.  Long-Distance Axonal Regeneration in the Transected Adult Rat Spinal Cord Is Promoted by Olfactory Ensheathing Glia Transplants , 1998, The Journal of Neuroscience.

[29]  F. Clarac,et al.  Gabaergic Control of Spinal Locomotor Networks in the Neonatal Rat , 1998, Annals of the New York Academy of Sciences.

[30]  S. Rumpel,et al.  Silent Synapses in the Developing Rat Visual Cortex: Evidence for Postsynaptic Expression of Synaptic Plasticity , 1998, The Journal of Neuroscience.

[31]  M. Schwartz,et al.  Implantation of stimulated homologous macrophages results in partial recovery of paraplegic rats , 1998, Nature Medicine.

[32]  Pattern Generators and Cortical Maps in Locomotion of Spinal Injured Rats a , 1998, Annals of the New York Academy of Sciences.

[33]  P. Reier,et al.  Spontaneous Functional Recovery in a Paralyzed Hemidiaphragm Following Upper Cervical Spinal Cord Injury in Adult Rats , 1999 .

[34]  J. Fawcett,et al.  The glial scar and central nervous system repair , 1999, Brain Research Bulletin.

[35]  E. Shimizu,et al.  Genetic enhancement of learning and memory in mice , 1999, Nature.

[36]  A. Gramsbergen,et al.  The activation of back muscles during locomotion in the developing rat. , 1999, Brain research. Developmental brain research.

[37]  J. Mcdonald,et al.  Transplanted embryonic stem cells survive, differentiate and promote recovery in injured rat spinal cord , 1999, Nature Medicine.

[38]  M. Bellingham Synaptic inhibition of cat phrenic motoneurons by internal intercostal nerve stimulation. , 1999, Journal of neurophysiology.

[39]  Jesús Avila,et al.  Functional Recovery of Paraplegic Rats and Motor Axon Regeneration in Their Spinal Cords by Olfactory Ensheathing Glia , 2000, Neuron.

[40]  M. Beattie,et al.  Review of current evidence for apoptosis after spinal cord injury. , 2000, Journal of neurotrauma.

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

[42]  H. Dai,et al.  Axonal Regeneration and Functional Recovery after Complete Spinal Cord Transection in Rats by Delayed Treatment with Transplants and Neurotrophins , 2001, The Journal of Neuroscience.

[43]  M. Oudega,et al.  Neurotrophins BDNF and NT-3 promote axonal re-entry into the distal host spinal cord through Schwann cell-seeded mini-channels. , 2001, The European journal of neuroscience.

[44]  S. Harkema,et al.  Retraining the injured spinal cord , 2001, The Journal of physiology.

[45]  K. Fouad,et al.  Anatomical Correlates of Locomotor Recovery Following Dorsal and Ventral Lesions of the Rat Spinal Cord , 2002, Experimental Neurology.

[46]  K. Fouad,et al.  Protective effects of oral creatine supplementation on spinal cord injury in rats , 2002, Spinal Cord.

[47]  S. Strittmatter,et al.  Nogo-66 receptor antagonist peptide promotes axonal regeneration , 2002, Nature.

[48]  Gong Ju,et al.  Spontaneous recovery of locomotion induced by remaining fibers after spinal cord transection in adult rats. , 2003, Restorative neurology and neuroscience.

[49]  X. Navarro,et al.  Olfactory ensheathing cells transplanted in lesioned spinal cord prevent loss of spinal cord parenchyma and promote functional recovery , 2003, Glia.

[50]  D. Fuller,et al.  Synaptic Pathways to Phrenic Motoneurons Are Enhanced by Chronic Intermittent Hypoxia after Cervical Spinal Cord Injury , 2003, The Journal of Neuroscience.

[51]  H. Goshgarian Invited Review: The crossed phrenic phenomenon: a model for plasticity in the respiratory pathways following spinal cord injury , 2003 .

[52]  M. Tuszynski,et al.  NT-3 gene delivery elicits growth of chronically injured corticospinal axons and modestly improves functional deficits after chronic scar resection , 2003, Experimental Neurology.

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

[54]  J. Esteban AMPA receptor trafficking: a road map for synaptic plasticity. , 2003, Molecular interventions.

[55]  H. Goshgarian The crossed phrenic phenomenon: a model for plasticity in the respiratory pathways following spinal cord injury. , 2003, Journal of applied physiology.

[56]  Margaret Fahnestock,et al.  Kindling and status epilepticus models of epilepsy: rewiring the brain , 2004, Progress in Neurobiology.

[57]  Martin E Schwab,et al.  The injured spinal cord spontaneously forms a new intraspinal circuit in adult rats , 2004, Nature Neuroscience.

[58]  O. A. Nikitin,et al.  Initiation of Locomotor Activity in Spinal Cats by Epidural Stimulation of the Spinal Cord , 2003, Neuroscience and Behavioral Physiology.

[59]  M. Stocker Ca2+-activated K+ channels: molecular determinants and function of the SK family , 2004, Nature Reviews Neuroscience.

[60]  Pavel Osten,et al.  Sindbis vector SINrep(nsP2S726): a tool for rapid heterologous expression with attenuated cytotoxicity in neurons , 2004, Journal of Neuroscience Methods.

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

[62]  K. Deisseroth,et al.  Millisecond-timescale, genetically targeted optical control of neural activity , 2005, Nature Neuroscience.

[63]  Gordon S. Mitchell,et al.  Spinal Synaptic Enhancement with Acute Intermittent Hypoxia Improves Respiratory Function after Chronic Cervical Spinal Cord Injury , 2005, The Journal of Neuroscience.

[64]  D. White,et al.  Phrenic long‐term facilitation requires NMDA receptors in the phrenic motonucleus in rats , 2005, The Journal of physiology.

[65]  H. Chiel,et al.  Fast noninvasive activation and inhibition of neural and network activity by vertebrate rhodopsin and green algae channelrhodopsin. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[66]  V. Edgerton,et al.  Hindlimb stepping movements in complete spinal rats induced by epidural spinal cord stimulation , 2005, Neuroscience Letters.

[67]  J. Feldman,et al.  Looking for inspiration: new perspectives on respiratory rhythm , 2006, Nature Reviews Neuroscience.

[68]  F. Frizelle,et al.  Colorectal motility and defecation after spinal cord injury in humans. , 2006, Progress in brain research.

[69]  R. Moreland,et al.  In vitro models: research in physiology and pharmacology of the lower urinary tract , 2006, British journal of pharmacology.

[70]  Jerry Silver,et al.  Combining an Autologous Peripheral Nervous System “Bridge” and Matrix Modification by Chondroitinase Allows Robust, Functional Regeneration beyond a Hemisection Lesion of the Adult Rat Spinal Cord , 2006, The Journal of Neuroscience.

[71]  R. Sidman,et al.  Physical activity-mediated functional recovery after spinal cord injury: potential roles of neural stem cells. , 2006, Regenerative medicine.

[72]  Jaideep Kapur,et al.  GABAergic Synaptic Inhibition Is Reduced before Seizure Onset in a Genetic Model of Cortical Malformation , 2006, The Journal of Neuroscience.

[73]  Feng Zhang,et al.  Channelrhodopsin-2 and optical control of excitable cells , 2006, Nature Methods.

[74]  A. Dolphin,et al.  A short history of voltage‐gated calcium channels , 2006, British journal of pharmacology.

[75]  P. Potter Disordered control of the urinary bladder after human spinal cord injury: what are the problems? , 2006, Progress in brain research.

[76]  M. Weller,et al.  Signaling from cAMP/PKA to MAPK and synaptic plasticity , 2003, Molecular Neurobiology.

[77]  Lu Sun,et al.  Activation of extrasynaptic NMDA receptors induces a PKC‐dependent switch in AMPA receptor subtypes in mouse cerebellar stellate cells , 2007, The Journal of physiology.

[78]  Benjamin R. Arenkiel,et al.  In Vivo Light-Induced Activation of Neural Circuitry in Transgenic Mice Expressing Channelrhodopsin-2 , 2007, Neuron.

[79]  L. Landmesser,et al.  New optical tools for controlling neuronal activity , 2007, Current Opinion in Neurobiology.

[80]  K. Nantwi,et al.  Effect of Spinal Cord Injury on the Respiratory System: Basic Research and Current Clinical Treatment Options , 2007, The journal of spinal cord medicine.

[81]  E. Bertram,et al.  The Relevance of Kindling for Human Epilepsy , 2007, Epilepsia.

[82]  Sergiy Yakovenko,et al.  Intraspinal stimulation caudal to spinal cord transections in rats. Testing the propriospinal hypothesis. , 2007, Journal of neurophysiology.

[83]  K. Deisseroth,et al.  Circuit-breakers: optical technologies for probing neural signals and systems , 2007, Nature Reviews Neuroscience.

[84]  T. Oertner,et al.  Optical induction of synaptic plasticity using a light-sensitive channel , 2007, Nature Methods.

[85]  Feng Zhang,et al.  Multimodal fast optical interrogation of neural circuitry , 2007, Nature.

[86]  Thomas G. Oertner,et al.  Optical induction of plasticity at single synapses reveals input-specific accumulation of αCaMKII , 2008, Proceedings of the National Academy of Sciences.

[87]  W. Alilain,et al.  Glutamate receptor plasticity and activity-regulated cytoskeletal associated protein regulation in the phrenic motor nucleus may mediate spontaneous recovery of the hemidiaphragm following chronic cervical spinal cord injury , 2008, Experimental Neurology.

[88]  W. C. Groat,et al.  The neural control of micturition , 2008, Nature Reviews Neuroscience.

[89]  K. Svoboda,et al.  Sparse optical microstimulation in barrel cortex drives learned behaviour in freely moving mice , 2008, Nature.

[90]  A. Williamson,et al.  Glutamate and astrocytes—Key players in human mesial temporal lobe epilepsy? , 2008, Epilepsia.

[91]  P. Reier,et al.  Respiratory neuroplasticity and cervical spinal cord injury: translational perspectives , 2008, Trends in Neurosciences.

[92]  Douglas S Kim,et al.  Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration , 2008, Nature Neuroscience.