Literature DB >> 114558

Cells of origin of long descending propriospinal fibers connecting the spinal enlargements in cat and monkey determined by horseradish peroxidase and electrophysiological techniques.

R D Skinner, J D Coulter, R J Adams, R S Remmel.   

Abstract

The cells of origin of the long descending propriospinal tract (LDPT) in the cervical enlargement were studied in cat and monkey by using the retrograde transport of horseradish peroxidase (HRP). Their distribution was confirmed electrophysiologically in cat by recording their antidromic action potentials. In cats and monkeys unilateral injections of HRP were made into the gray matter of the lumbosacral enlargement, but there was some spread to the contralateral side. In cats labeled somas were found in greatest numbers in lamina VIII and medial lamina VII, bilaterally. Labeled cells also were found bilaterally in laminae I, IV--VI, and X, but few were in IV and VI. Those in lamina V were usually in the lateral part of the lamina near the reticulated region. The cross-sectional areas of 20 neurons from each of laminae I and V--VIII were measured. Cells in lamina I were smallest and the largest were in VII and VIII. In cats with the spinal cord hemisected between the injection site and the cervical enlargement containing the somas, the bilaterality of the LDPT neurons in laminae VII and VIII was confirmed anatomically and physiologically. Contralaterally projecting neurons in laminae VIII and medial VII constituted a majority of LDPT cells in those laminae. The LDPT neurons in the dorsal horn appeared to project mainly ipsilaterally, but the number of labeled dorsal horn cells in these preparations was small. The distribution of antidromically localized cells of the LDPT was found to be in good agreement with the anatomical results. Their conduction velocity was 59 +/- 22 m/s (mean +/- s.d., n = 245). Histograms of the conduction velocity by laminae are given. In monkey the distribution of labeled somas was similar to that in the cat, except that the concentration of labeled somas in the ventral horn was more medially and dorsally located. Labeled somas were found bilaterally in laminae I, IV--VIII, and X, but more appeared to be ipsilateral to the side of the injection, especially in the dorsal horn. The bilaterality of the LDPT in the monkey was not tested with hemisections of the spinal cord. Neurons of the LDPT are ideally situated for conveying sensory information from the forelimb for eliciting reflexes in the hindlimb, as has been observed after stimulating afferents in the forelimb, and for coordinating, in general, motor functions between the two pairs of limbs.

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Year:  1979        PMID: 114558     DOI: 10.1002/cne.901880307

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  16 in total

1.  Magnetically evoked inter-enlargement response: an assessment of ascending propriospinal fibers following spinal cord injury.

Authors:  Eric Beaumont; Stephen M Onifer; William R Reed; David S K Magnuson
Journal:  Exp Neurol       Date:  2006-06-22       Impact factor: 5.330

2.  Propriospinal neurons contribute to bulbospinal transmission of the locomotor command signal in the neonatal rat spinal cord.

Authors:  Eugene Zaporozhets; Kristine C Cowley; Brian J Schmidt
Journal:  J Physiol       Date:  2006-02-09       Impact factor: 5.182

3.  Propriospinal neurons are sufficient for bulbospinal transmission of the locomotor command signal in the neonatal rat spinal cord.

Authors:  Kristine C Cowley; Eugene Zaporozhets; Brian J Schmidt
Journal:  J Physiol       Date:  2008-01-31       Impact factor: 5.182

Review 4.  Schwann cell transplantation and descending propriospinal regeneration after spinal cord injury.

Authors:  Ling-Xiao Deng; Chandler Walker; Xiao-Ming Xu
Journal:  Brain Res       Date:  2014-09-26       Impact factor: 3.252

5.  Evidence for sequential degeneration of the neurons in the intermediate zone of the spinal cord in amyotrophic lateral sclerosis: a topographic and quantitative investigation.

Authors:  K Oyanagi; F Ikuta; Y Horikawa
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

6.  Branching neurons in the cervical spinal cord: a retrograde fluorescent double-labeling study in the rat.

Authors:  C A Verburgh; H G Kuypers
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

7.  Anatomical Plasticity of Rostrally Terminating Axons as a Possible Bridging Substrate across a Spinal Injury.

Authors:  Adele E Doperalski; Lynnette R Montgomery; Sarah E Mondello; Dena R Howland
Journal:  J Neurotrauma       Date:  2019-12-23       Impact factor: 5.269

Review 8.  The neural control of interlimb coordination during mammalian locomotion.

Authors:  Alain Frigon
Journal:  J Neurophysiol       Date:  2017-03-15       Impact factor: 2.714

9.  Disease-specific patterns of neuronal loss in the spinal ventral horn in amyotrophic lateral sclerosis, multiple system atrophy and X-linked recessive bulbospinal neuronopathy, with special reference to the loss of small neurons in the intermediate zone.

Authors:  S Terao; G Sobue; Y Hashizume; T Mitsuma; A Takahashi
Journal:  J Neurol       Date:  1994-02       Impact factor: 4.849

10.  Anterograde labeling of ventrolateral funiculus pathways with spinal enlargement connections in the adult rat spinal cord.

Authors:  William R Reed; Alice Shum-Siu; Ashley Whelan; Stephen M Onifer; David S K Magnuson
Journal:  Brain Res       Date:  2009-09-18       Impact factor: 3.252

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