Literature DB >> 50333

Golgi studies in the substantia gelatinosa neurons in the spinal trigeminal nucleus.

S Gobel.   

Abstract

This Golgi study identifies three neuronal cell types in the substantia gelatinosa (SG) layer of the spinal trigeminal nucleus. The SG neurons are distinguished from each other based on: (1) dendritic branching pattern, (2) denritic spine distribution, (3) geometric shape of the denritic tree, (4) laminar distribution of the dendrites, (5) axonal branching pattern and (6) laminar distribution of the axonal arbor. The islet cell is found in small clusters and its dendrites and axonal arbor are confined within the SG layer. Its dendrites span the full width of the SG layer and extend up to 500 mum in the long axis of the layer. Dendritic spines are generally sparse with small clusters of spines found on the higher order dendritic branches. The islet cell axon extends for at least 1 mm in the long axis of the layer. Each of its collaterals divide every 50-100 mum with one branch doubling back in the direction of the cell body and the other branch continuing on in the direction of its parent. In this manner each islet cell generates a profuse axonal plexus in the SG layer. The stalked cell is found individually within the SG layer. Its cell body is usually found in the inner half of the SG layer and its sinuous dendrites cross the SG layer and enter the marginal layer. The stalked cell dendrites emit numerous fine stalk-like branches and dentritic spines. Its axon emits branches in the SG and marginal layers. The spiny cell is found singly between groups of islet cells. Its extensive dendritic tree spans up to 500 mum rostrocaudally and mediolaterally crossing into both the marginal and magnocellular layers. Spiny cells have evenly distributed dendritic spines along their dendrites in the SG layer. The spiny cell axon sends branches into all three layers of nucleus caudalis. Numerous branches enter the outer 300 mum of the magnocellular layer where they undergo further branching with some branches returning in recurrent fashion toward the SG layer. The three neuronal cell types of the SG layer satisfy all of the morphological criteria for Golgi type II interneurons. Their highly branched axons generate many collaterals within the confines of their dendritic trees and do not project out of nucleus caudalis. The SG neurons are considered to be inhibitory interneurons interposed between V nerve primary afferent axons which arborize in the SG layer and second order neurons of nucleus caudalis.

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Year:  1975        PMID: 50333     DOI: 10.1002/cne.901620308

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


  25 in total

1.  Correlations between neuronal morphology and electrophysiological features in the rodent superficial dorsal horn.

Authors:  T J Grudt; E R Perl
Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

2.  The grey matter of the dorsal horn of the adult human spinal cord, including comparisons with general somatic and visceral efferent cranial nerve nuclei.

Authors:  T E Abdel-Maguid; D Bowsher
Journal:  J Anat       Date:  1985-10       Impact factor: 2.610

3.  Neurons with asymmetrical dendritic arbors in the substantia gelatinosa of the rat spinal cord.

Authors:  J A Beal; K N Nandi; D S Knight
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

4.  Morphology of inhibitory and excitatory interneurons in superficial laminae of the rat dorsal horn.

Authors:  David J Maxwell; Mino D Belle; Ornsiri Cheunsuang; Anika Stewart; Richard Morris
Journal:  J Physiol       Date:  2007-08-23       Impact factor: 5.182

Review 5.  Neuropeptide gene expression and neural activity: assessing a working hypothesis in nucleus caudalis and dorsal horn neurons expressing preproenkephalin and preprodynorphin.

Authors:  G R Uhl; T Nishimori
Journal:  Cell Mol Neurobiol       Date:  1990-03       Impact factor: 5.046

6.  Nociceptive neurones in the superficial dorsal horn of cat lumbar spinal cord and their primary afferent inputs.

Authors:  W M Steedman; V Molony; A Iggo
Journal:  Exp Brain Res       Date:  1985       Impact factor: 1.972

7.  The morphology of Golgi-stained neurons in lamina II of the rat spinal cord.

Authors:  A J Todd; S G Lewis
Journal:  J Anat       Date:  1986-12       Impact factor: 2.610

Review 8.  Transmitting pain and itch messages: a contemporary view of the spinal cord circuits that generate gate control.

Authors:  João Braz; Carlos Solorzano; Xidao Wang; Allan I Basbaum
Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

9.  Neurokinin-1 receptor immunoreactive neuronal elements in the superficial dorsal horn of the chicken spinal cord: with special reference to their relationship with the tachykinin-containing central axon terminals in synaptic glomeruli.

Authors:  Hiroshi Sakamoto; Toyoko Kawate; Yongnan Li; Saoko Atsumi
Journal:  Acta Histochem Cytochem       Date:  2009-07-15       Impact factor: 1.938

10.  Quantitative characterization of low-threshold mechanoreceptor inputs to lamina I spinoparabrachial neurons in the rat.

Authors:  David Andrew
Journal:  J Physiol       Date:  2009-11-23       Impact factor: 5.182

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