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Spinal locomotion

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Spinal locomotion results from intricate dynamic interactions between a central program in lower thoracolumbar spine and proprioceptive feedback from body in the absence of central control by brain as in complete spinal cord injury (SCI).[1][2][3] Following SCI, the spinal circuitry below the lesion site does not become silent rather it continues to maintain active and functional neuronal properties although in a modified manner.[4][5]

Components of spinal locomotionEdit

File:Anatomy and physiology of animals Relation btw sensory, relay & motor neurons.jpg

Centrally generated patternsEdit

The spinal cord executes rhythmical and sequential activation of muscles in locomotion. The central pattern generator (CPG) provides the basic locomotor rhythm and synergies by integrating commands from various sources that serve to initiate or modulate its output to meet the requirements of the environment. CPG within the lumbosacral spinal cord segments represent an important component of the total circuitry that generates and controls posture and locomotion.[6] This spinal circuitry can function independently in the absence of descending input from the brain to generate stable posture and locomotion and even modulate activity to match changing conditions (e.g., stepping over obstacles).[7] This capability improve with training (spinal plasticity)[8] and therefore it is believed that spinal cord has the capability to learn and memorize.[9][10]

Sensory feedbackEdit

The sensory feedback originates from muscles, joints, tendons and skin afferents as well as from special senses and dynamically adapts the locomotor pattern of spinal cord to the requirements of the environment. These afferent sensory receptors perceive deformation of tissue the amount of pressure (stretch or simply, placement), direction of movement, speed and velocity at which movement is occurring.

Sensory modulation of CPGEdit

File:Nervous system organization en.svg

The dynamic interactions between Spinal cord and sensory input are ensured by modulating transmission in locomotor pathways in a state- and phase-dependent manner. For instance, proprioceptive inputs from extensors can, during stance, adjust the timing and amplitude of muscle activities of the limbs to the speed of locomotion but be silenced during the swing phase of the cycle. Similarly, skin afferents participate predominantly in the correction of limb and foot placement during stance on uneven terrain, but skin stimuli can evoke different types of responses depending on when they occur within the step cycle.[11] It is important to note that inputs from the hip appear to play a critical role in spinal locomotion. Experiments on spinal animals showed that when one limb is held with the hip flexed, locomotion on that side stops while the other limb continues walking. However, when the stopped limb is extended at the hip joint to a point normally reached at the end of stance during walking, it suddenly flexes and starts walking again provided that the contralateral limb is a position to accept the weight of the hindquarters.[12] Other work confirmed the importance of hip afferents for locomotor rhythm generation since flexion of the hip will abolish the rhythm whereas extension will enhance it.[13]

The spinal cord processes and interprets proprioception in a manner similar to how our visual system processes information.[14] When we view a painting, the brain interprets the total visual field, as opposed to processing each individual pixel of information independently, and then derives an image. At any instant the spinal cord receives an ensemble of information from all receptors throughout the body that signals a proprioceptive “image” that represents time and space, and it computes which neurons to excite next based on the most recently perceived “images.” The importance of the CPG is not simply its ability to generate repetitive cycles, but also to receive, interpret, and predict the appropriate sequences of actions during any part of the step cycle, i.e., state dependence. The peripheral input then provides important information from which the probabilities of a given set of neurons being active at any given time can be finely tuned to a given situation during a specific phase of a step cycle. An excellent example of this is when a mechanical stimulus is applied to the dorsum of the paw of a cat. When the stimulus is applied during the swing phase, the flexor muscles of that limb are excited, and the result is enhanced flexion in order to step over the obstacle that created the stimulus.[15] However, when the same stimulus is applied during stance, the extensors are excited. Thus, the functional connectivity between mechanoreceptors and specific interneuronal populations within the spinal cord varies according to the physiological state. Even the efficacy of the monosynaptic input from muscle spindles to the motor neuron changes readily from one part of the step cycle to another, according to whether a subject is running or walking.[16]

In the absence of CPG, control by brain as it happens in complete spinal cord injury, sensory feedback is very important in generating rhythmic locomotion. Firstly, locomotor movements can be initiated or blocked by some proprioceptive afferent inputs.[12] Other work confirmed the importance of hip afferents for locomotor rhythm generation since flexion of the hip will abolish the rhythm whereas extension will enhance it.[13] Secondly, proprioceptive afferents may participate in adapting walking speed, in determining overall cycle duration, and in regulating the structure of the step cycle’s subphases (i.e., swing, stance), which is required for speed adaptation and interlimb coupling.[16][17] Thirdly, proprioceptive afferents are involved in setting the level of muscle activity through various reflex pathways.[18]

Developmental evidenceEdit

Ultrasound recordings have captured in utero images of human fetuses at 13–14 gestational weeks "creeping and climbing" and producing alternating steps.[19] Onset of stepping in the fetus precedes development and myelinition of most descending brain pathways strongly suggesting human spinal cord locomotor CPG and sensory feedback coordination and plasticity. Collectively, studies across the first postnatal year indicates that a locomotor continuum extends from neonatal stepping to the onset of independent walking further suggesting human locomotion is controlled by CPG and sensory input interaction.

RehabilitationEdit

The injured spinal cord is an “altered” spinal cord. After a SCI, supraspinal and spinal sources of control of movement differ substantially from that which existed prior to the injury,[20] thus resulting in an altered spinal cord. The automaticity of posture and locomotion emerge from the interactions between peripheral nervous system (PNS) and central nervous system (CNS) to work in synergy, each system having intrinsic activation and inhibition patterns that can generate coordinated motor outputs.

Electrical stimulationEdit

Numerous experiments have demonstrated that electrical stimulation (ES) of the lumbosacral enlargement and dorsal root can induce locomotor EMG patterns and even hindlimb stepping in acute and chronic low-spinal animals and humans.[21][22] Increased stimulation amplitude resulted in increased EMG amplitudes and an increased frequency of rhythmic activity. High frequencies of stimulation (>70 Hz) produced tonic activity in the leg musculature, which suggests that the upper lumbar stimulation may activate neuronal structures that then recruit interneurons involved in CPG.[23]

Treadmill trainingEdit

Treadmill training (more commonly known as body weight supported treadmill training) can be applied via manual (therapist) or robotic assistance. In manual treadmill training the therapists provide assistance to facilitate an upright posture and a normal stepping pattern.[24] Therapist assistance may be provided at the patient’s pelvis, leg and foot, and a third therapist controlling the treadmill settings.[25] In robotic-assisted treadmill training, a device replaces the need for therapists to assist the patient in generating a normal stepping pattern. Currently, there are three different models available: Hocoma's Lokomat, the HealthSouth AutoAmbulator, and the Mechanized Gait Trainer II.[25] The Lokomat is a driven gait orthosis that consists of a computer -controlled exoskeleton that secured to the patient’s legs while being supported over a treadmill.[24] In addition to a belt driven treadmill and an overhead lift, the HealthSouth AutoAmbulator also includes a pair of articulated arms (that drives the hip and knee joints) and two upright structures that house the computer controls and body-weight unloading mechanism.[25] Unlike the first two, the Mechanized Gait Trainer II does not work in conjunction with a treadmill; instead it is based on a crank and rocker gear system which provides limb motion similar to an elliptical trainer.[25] Robotic-assisted treadmill training was developed with three goals in mind: 1. to decrease therapist physical demand and time, 2. to improve repeatability of step kinematics, and 3. to increase volume of locomotor training.[25]

In Humans with clinically complete SCI, there is evidence that treadmill training can improve several aspects of walking with some weight support assistance. Dietz and colleagues reported that after several weeks of treadmill training, the levels of weight bearing that can be imposed on the legs of clinically complete SCI subjects during treadmill walking significantly increases.[26] When stepping on a treadmill with body-weight support, rhythmic leg muscle activation patterns can be elicited in clinically complete subjects who are otherwise unable to voluntarily produce muscle activity in their legs.[27] A recent study has demonstrated that the levels of leg extensor muscle activity recorded in clinically complete SCI subjects significantly improved over course of several weeks of step training.[28] Interestingly, the stepping ability of clinically complete SCI subjects can improve in response to step training, but the level of improvement has not reached a level that allows complete independence from assistance during full weight-bearing. Largely due to the knowledge gained from studies on spinalized animals, two general principles have emerged for exciting the spinal circuits that generate stepping:

  • Body weight–supported treadmill training improves the ability of the lumbosacral spinal cord to generate weight-bearing stepping.
  • Patterns of sensory input provided during locomotor training are critical for driving the plasticity that mediates locomotor recovery.

See alsoEdit

ReferencesEdit

  1. , Edgerton et al, 1998a. Locomotor capacity attributable to step training versus spontaneous recovery after spinalization in adult cats. J. Neurophysiol 79:1329–40
  2. Edgerton et al, 1999a. Retention of hindlimb stepping ability in adult spinal cats after the cessation of step training. J. Neurophysiol. 81:85–94
  3. Edgerton et al, 2002. Use of robotics in assessing the adaptive capacity of the rat lumbar spinal cord. Prog. Brain Res. 137:141–49
  4. Edgerton, V.R., Harkema, S.J., Dobkin, B.H. 2003. Retraining the Human Spinal Cord In: Spinal Cord Medicine: Principles and Practices. Demos Medical Publishing, Chapter 60 817-826
  5. de Leon, R.D., Roy, R.R., and Edgerton, V.R.2001 Is the recovery of stepping following spinal cord injury mediated by modifying existing neural pathways or by generating new pathways? Phys. Therapy 81(12): 1904-1911
  6. Dietz 2003. spinal cord pattern generators for locomotion. Clin Neurophysiol. 114:1379–89
  7. Forssberg H, Grillner S, Rossignol S. 1975 Phase dependent reflex reversal during walking in chronic spinal cats. Brain Res. 85:103–7
  8. Dietz 2003. Spinal cord pattern generators for locomotion. Clin. Neurophysiol. 114:1379–89
  9. Garraway SM, Hochman S. 2001. Serotonin increases the incidence of primary afferentevoked long-term depression in rat deep dorsal horn neurons. J. Neurophysiol. 85:1864–72
  10. Rygh LJ, Tjolsen A, Hole K, Svendsen F. 2002. Cellular memory in spinal nociceptive circuitry.Scand. J. Psychol. 43:153–59
  11. Simonsen EB, Dyhre-Poulsen P. 1999. Amplitude of the human soleus H reflex during walking and running. J. Physiol.515:929–39
  12. 12.0 12.1 Grillner, S., Rossignol, S., 1978. On the initiation of the swing phase of locomotion in chronic spinal cats. Brain Res. 146, 269–277
  13. 13.0 13.1 Pearson, K.G., Rossignol, S., 1991. Fictive motor patterns in chronic spinal cats. J. Neurophysiol. 66, 1874–1887
  14. Reggie Edgerton 2004. Plasticity of the spinal neural circitry after injury Annu. Rev. Neurosci. 27:145–67
  15. Forssberg H.1979 Stumbling corrective reaction: a phase-dependent compensatory reaction during locomotion. J Neurophysiol 42:936–953
  16. 16.0 16.1 Lovely RG, Gregor RJ, Roy RR, Edgerton VR.1990. Weight-bearing hindlimb stepping in treadmill-exercised adult spinal cats. Brain Res. 514:206–18
  17. Zehret al,2003 Neural control of rhythmic human arm movement: phase dependence and task modulation of Hoffmann reflexes in forearm muscles. J. Neurophysiol. 89:12–21
  18. Duysens J, Pearson KG. 1980. Inhibition of flexor burst generation by loading ankle extensor muscles in walking cats. Brain Res.187:321–32
  19. Ianniruberto and Tajani Ultrasonographic study of fetal movements. Semin Perinatol 5: 175–181, 1981.[Web of Science][Medline]
  20. Dietz et al, 1998b. Locomotor pattern in paraplegic patients: training effects and recovery of spinal cord function. Spinal Cord 36:380–90
  21. Grillner S, Zangger P. 1984. The effect of dorsal root transection on the efferent motor pattern in the cat’s hindlimb during locomotion. Acta Physiol. Scand. 120:393–405
  22. Gerasimenko YP, Avelev VD, Nikitin OA, Lavrov IA. 2003. Initiation of locomotor activity in spinal cats by epidural stimulation of the spinal cord. Neurosci. Behav.Physiol.33:247–54
  23. Dimitrijevic MR, Gerasimenko Y, Pinter MM.1998. Evidence for a spinal central pattern generator in humans. Ann. NY Acad. Sci.860:360–76
  24. 24.0 24.1 Hornby, George T., Zemon, David H., & Campbell, Donielle. 2005. Robotic-assisted body weight supported treadmill training in individuals following motor incomplete spinal cord injury. Physical Therapy, 85(1), 52-66.
  25. 25.0 25.1 25.2 25.3 25.4 Winchester, Patricia & Querry, Ross. 2006. Robotic-orthoses for body weight supported treadmill training. Physical Medicine and Rehabilitation Clinics of North America, 17(1), 159-172.
  26. Dietz V, Colombo G, Jensen L, Baumgartner L.1995. Locomotor capacity of spinal cord in paraplegic patients. Ann. Neurol. 37:574–82
  27. Maegele M, Muller S,Wernig A, Edgerton VR,Harkema SJ. 2002. Recruitment of spinal motor pools during voluntary movements versus stepping after human spinal cord injury. J. Neurotrauma 19:1217–29
  28. Wirz M, Colombo G, Dietz V. 2001. Long term effects of locomotor training in spinal man. J. Neurol. Neurosurg. Psychiatry 71:93–96

External linksEdit

Spinal cord

epidural space, dura mater, subdural space, arachnoid mater, subarachnoid space, pia mater, denticulate ligaments, conus medullaris, cauda equina, filum terminale, cervical enlargement, lumbar enlargement, anterior median fissure, dorsal root, dorsal root ganglion, dorsal ramus, ventral root, ventral ramus, sympathetic trunk, gray ramus communicans, white ramus communicans

grey matter: central canal, substantia gelatinosa of Rolando, reticular formation, substantia gelatinosa centralis, interneuron, anterior horn, lateral horn, posterior horn (column of Clarke, dorsal spinocerebellar tract)

white matter: anterior funiculus: descending (anterior corticospinal tract, vestibulospinal fasciculus, tectospinal tract), ascending (anterior spinothalamic tract, anterior proper fasciculus)

lateral funiculus: descending (lateral corticospinal tract, rubrospinal tract, olivospinal tract), ascending dorsal spinocerebellar tract, ventral spinocerebellar tract, spinothalamic tract, lateral spinothalamic tract, anterior spinothalamic tract, spinotectal tract, posterolateral tract, lateral proper fasciculus, medial longitudinal fasciculus

posterior funiculus: fasciculus gracilis, fasciculus cuneatus, posterior proper fasciculus


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