Literature DB >> 9987039

Effects of dorsolateral spinal lesions on stretch reflex threshold and stiffness in awake cats.

J Taylor1, J Munson, C Vierck.   

Abstract

Measurements of threshold angle and incremental dynamic stiffness (IDS) were derived from triceps surae stretch reflexes, elicited by ramp and hold flexion at the ankle joint of four cats that were tested while awake. Stretch reflexes were assessed from trials that began from different ankle joint start positions or were matched using a post-hoc analysis for initial background force during testing sessions before and following unilateral lesions of the dorsolateral funiculus at levels ranging from T13 to L3. Unilateral lesions of the dorsolateral funiculus (DLF) produced significant ipsilateral decreases in stretch reflex threshold and increases in reflex gain, measured as incremental dynamic stiffness (IDS). ANCOVA testing indicated that the reduction in threshold, but not the increase in IDS, was dependent upon the level of background force. Reflex testing from different start angles demonstrated that DLF lesions diminished the correlation between threshold and IDS. Intravenous infusion of ketamine dose-dependently reduced IDS, compared with testing in the unanaesthetized state. Postoperative reflex testing during infusion of ketamine at 22.2 mg/kg per h, when electromyographic responses were reduced to 24% of control levels, abolished differences in IDS between the ipsilateral and contralateral hindlimbs. These and related observations suggest that the postoperative increase in IDS in awake animals was not due to an increase in passive stiffness.

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Year:  1999        PMID: 9987039     DOI: 10.1046/j.1460-9568.1999.00468.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  5 in total

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Authors:  Raffaele Nardone; Yvonne Höller; Aljoscha Thomschewski; Peter Höller; Piergiorgio Lochner; Stefan Golaszewski; Francesco Brigo; Eugen Trinka
Journal:  J Neural Transm (Vienna)       Date:  2014-05-28       Impact factor: 3.575

2.  Polysynaptic excitatory postsynaptic potentials that trigger spasms after spinal cord injury in rats are inhibited by 5-HT1B and 5-HT1F receptors.

Authors:  Katherine C Murray; Marilee J Stephens; Michelle Rank; Jessica D'Amico; Monica A Gorassini; David J Bennett
Journal:  J Neurophysiol       Date:  2011-06-08       Impact factor: 2.714

3.  Spasticity therapy reacts to astrocyte GluA1 receptor upregulation following spinal cord injury.

Authors:  Julio Gómez-Soriano; Eider Goiriena; Julian Taylor
Journal:  Br J Pharmacol       Date:  2010-11       Impact factor: 8.739

4.  Treatment of rat spinal cord injury with the neurotrophic factor albumin-oleic acid: translational application for paralysis, spasticity and pain.

Authors:  Gerardo Avila-Martin; Iriana Galan-Arriero; Julio Gómez-Soriano; Julian Taylor
Journal:  PLoS One       Date:  2011-10-26       Impact factor: 3.240

5.  Thoracic 9 Spinal Transection-Induced Model of Muscle Spasticity in the Rat: A Systematic Electrophysiological and Histopathological Characterization.

Authors:  Jose A Corleto; Mariana Bravo-Hernández; Kota Kamizato; Osamu Kakinohana; Camila Santucci; Michael R Navarro; Oleksandr Platoshyn; Dasa Cizkova; Nadezda Lukacova; Julian Taylor; Martin Marsala
Journal:  PLoS One       Date:  2015-12-29       Impact factor: 3.240

  5 in total

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