Literature DB >> 18674601

Timing in the absence of supraspinal input I: variable, but not fixed, spaced stimulation of the sciatic nerve undermines spinally-mediated instrumental learning.

K M Baumbauer1, K C Hoy, J R Huie, A J Hughes, S A Woller, D A Puga, B Setlow, J W Grau.   

Abstract

Rats with complete spinal transections are capable of acquiring a simple instrumentally trained response. If rats receive shock to one hind limb when the limb is extended (controllable shock), the spinal cord will learn to hold the leg in a flexed position that minimizes shock exposure. If shock is delivered irrespective of leg position, subjects do not exhibit an increase in flexion duration and subsequently fail to learn when tested with controllable shock (learning deficit). Just 6 min of variable intermittent shock produces a learning deficit that lasts 24 h. Evidence suggests that the neural mechanisms underlying the learning deficit may be related to those involved in other instances of spinal plasticity (e.g. windup, long-term potentiation). The present paper begins to explore these relations by demonstrating that direct stimulation of the sciatic nerve also impairs instrumental learning. Six minutes of electrical stimulation (mono- or biphasic direct current [DC]) of the sciatic nerve in spinally transected rats produced a voltage-dependent learning deficit that persisted for 24 h (experiments 1-2) and was dependent on C-fiber activation (experiment 7). Exposure to continuous stimulation did not produce a deficit, but intermittent burst or single pulse (as short as 0.1 ms) stimulation (delivered at a frequency of 0.5 Hz) did, irrespective of the pattern (fixed or variable) of stimulus delivery (experiments 3-6, 8). When the duration of stimulation was extended from 6 to 30 min, a surprising result emerged; shocks applied in a random (variable) fashion impaired subsequent learning whereas shocks given in a regular pattern (fixed spacing) did not (experiments 9-10). The results imply that spinal neurons are sensitive to temporal relations and that stimulation at regular intervals can have a restorative effect.

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Year:  2008        PMID: 18674601      PMCID: PMC2633135          DOI: 10.1016/j.neuroscience.2008.07.003

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  81 in total

Review 1.  Cerebellar function: coordination, learning or timing?

Authors:  M D Mauk; J F Medina; W L Nores; T Ohyama
Journal:  Curr Biol       Date:  2000-07-13       Impact factor: 10.834

2.  Classical conditioning, sensitization and habituation in the spinal cat.

Authors:  R G Durkovic
Journal:  Physiol Behav       Date:  1975-03

3.  Instrumental learning within the spinal cord: III. Prior exposure to noncontingent shock induces a behavioral deficit that is blocked by an opioid antagonist.

Authors:  Robin L Joynes; James W Grau
Journal:  Neurobiol Learn Mem       Date:  2004-07       Impact factor: 2.877

4.  Neonatal hind-paw injury disrupts acquisition of an instrumental response in adult spinal rats.

Authors:  Erin E Young; Kyle M Baumbauer; Audrea Elliot; Robin L Joynes
Journal:  Behav Neurosci       Date:  2007-10       Impact factor: 1.912

5.  Pharmacological activation and modulation of the central pattern generator for locomotion in the cat.

Authors:  S Rossignol; C Chau; E Brustein; N Giroux; L Bouyer; H Barbeau; T A Reader
Journal:  Ann N Y Acad Sci       Date:  1998-11-16       Impact factor: 5.691

6.  Low-frequency stimulation of afferent Adelta-fibers induces long-term depression at primary afferent synapses with substantia gelatinosa neurons in the rat.

Authors:  J Sandkühler; J G Chen; G Cheng; M Randić
Journal:  J Neurosci       Date:  1997-08-15       Impact factor: 6.167

7.  Progressive tactile hypersensitivity: an inflammation-induced incremental increase in the excitability of the spinal cord.

Authors:  Qing-Ping Ma; Clifford J Woolf
Journal:  Pain       Date:  1996-09       Impact factor: 6.961

8.  Instrumental learning within the spinal cord: IV. Induction and retention of the behavioral deficit observed after noncontingent shock.

Authors:  Eric D Crown; Adam R Ferguson; Robin L Joynes; James W Grau
Journal:  Behav Neurosci       Date:  2002-12       Impact factor: 1.912

9.  Evidence for a central component of post-injury pain hypersensitivity.

Authors:  C J Woolf
Journal:  Nature       Date:  1983 Dec 15-21       Impact factor: 49.962

10.  Mechanoreceptors in rat glabrous skin: redevelopment of function after nerve crush.

Authors:  K H Sanders; M Zimmermann
Journal:  J Neurophysiol       Date:  1986-04       Impact factor: 2.714

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  26 in total

Review 1.  Learning to promote recovery after spinal cord injury.

Authors:  James W Grau; Rachel E Baine; Paris A Bean; Jacob A Davis; Gizelle N Fauss; Melissa K Henwood; Kelsey E Hudson; David T Johnston; Megan M Tarbet; Misty M Strain
Journal:  Exp Neurol       Date:  2020-04-28       Impact factor: 5.330

Review 2.  What Is Being Trained? How Divergent Forms of Plasticity Compete To Shape Locomotor Recovery after Spinal Cord Injury.

Authors:  J Russell Huie; Kazuhito Morioka; Jenny Haefeli; Adam R Ferguson
Journal:  J Neurotrauma       Date:  2017-01-13       Impact factor: 5.269

3.  Peripheral noxious stimulation reduces withdrawal threshold to mechanical stimuli after spinal cord injury: role of tumor necrosis factor alpha and apoptosis.

Authors:  Sandra M Garraway; Sarah A Woller; J Russell Huie; John J Hartman; Michelle A Hook; Rajesh C Miranda; Yung-Jen Huang; Adam R Ferguson; James W Grau
Journal:  Pain       Date:  2014-08-29       Impact factor: 6.961

4.  Brain-derived neurotrophic factor promotes adaptive plasticity within the spinal cord and mediates the beneficial effects of controllable stimulation.

Authors:  J R Huie; S M Garraway; K M Baumbauer; K C Hoy; B S Beas; K S Montgomery; J L Bizon; J W Grau
Journal:  Neuroscience       Date:  2011-10-25       Impact factor: 3.590

5.  A brief period of moderate noxious stimulation induces hemorrhage and impairs locomotor recovery after spinal cord injury.

Authors:  Misty M Strain; Michelle A Hook; Joshua D Reynolds; Yung-Jen Huang; Melissa K Henwood; James W Grau
Journal:  Physiol Behav       Date:  2019-10-21

6.  Intermittent apnea elicits inactivity-induced phrenic motor facilitation via a retinoic acid- and protein synthesis-dependent pathway.

Authors:  Nathan A Baertsch; Tracy L Baker
Journal:  J Neurophysiol       Date:  2017-08-16       Impact factor: 2.714

7.  Timing in the absence of supraspinal input III: regularly spaced cutaneous stimulation prevents and reverses the spinal learning deficit produced by peripheral inflammation.

Authors:  Kyle M Baumbauer; James W Grau
Journal:  Behav Neurosci       Date:  2011-02       Impact factor: 1.912

8.  Temporal regularity determines the impact of electrical stimulation on tactile reactivity and response to capsaicin in spinally transected rats.

Authors:  K M Baumbauer; K H Lee; D A Puga; S A Woller; A J Hughes; J W Grau
Journal:  Neuroscience       Date:  2012-10-02       Impact factor: 3.590

9.  Inactivity-induced phrenic and hypoglossal motor facilitation are differentially expressed following intermittent vs. sustained neural apnea.

Authors:  N A Baertsch; T L Baker-Herman
Journal:  J Appl Physiol (1985)       Date:  2013-03-14

10.  Timing in the absence of supraspinal input II: regularly spaced stimulation induces a lasting alteration in spinal function that depends on the NMDA receptor, BDNF release, and protein synthesis.

Authors:  Kyle M Baumbauer; John R Huie; Abbey J Hughes; James W Grau
Journal:  J Neurosci       Date:  2009-11-18       Impact factor: 6.167

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