Literature DB >> 2808777

Morphology and somatotopic organization of the central terminals of hindlimb hair follicle afferents in the rat lumbar spinal cord.

P Shortland1, C J Woolf, M Fitzgerald.   

Abstract

The morphology of the central collateral arborizations of 24 A-beta hair follicle afferents (HFAs) innervating different regions of the skin of the hindlimb were studied by the intra-axonal injection of horseradish peroxidase (HRP) in adult rats. A total of 236 collaterals were recovered. These fell into three classes--complex, simple, and blind-ending--based on numbers of boutons and terminal branch patterns. The morphology of the HFA central arbors innervating the lateral and medial leg and dorsum of the foot was flame-shaped. Afferents with receptive fields on the glabrous-hairy skin border consistently had extra terminal branches running ventromedially into laminae IV/V. Differences in the width of terminal arbors were found. HFA terminals innervating the lateral leg formed narrower sheets than those innervating the dorsum of the foot and toes. The somatotopic organization of the collaterals and terminal arborizations of individual afferents were analyzed both by considering all the collaterals along an axon's rostrocaudal extent and by only examining arbors with boutons (the complex and simple arbors). Thirty-seven percent of blind-ending and 18% of simple collaterals were found to overlap in the rostrocaudal direction with the complex arborizations of afferents whose receptive fields were in a different cutaneous nerve territory. There was no overlap between complex arborizations of afferents from different nerve territories. However, the complex arbors of afferents with receptive fields within a particular nerve territory showed considerable terminal overlap even if they had nonadjacent peripheral receptive fields. The topographical organization of the central terminals of HFAs, forms a coarse somatotopic map of overlapping terminals whereby a particular region of dorsal horn has a maximal, but not exclusive, input from a particular area of skin.

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Year:  1989        PMID: 2808777     DOI: 10.1002/cne.902890307

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


  19 in total

1.  Synaptic reorganization in the substantia gelatinosa after peripheral nerve neuroma formation: aberrant innervation of lamina II neurons by Abeta afferents.

Authors:  I Kohama; K Ishikawa; J D Kocsis
Journal:  J Neurosci       Date:  2000-02-15       Impact factor: 6.167

2.  Lack of evidence for sprouting of Abeta afferents into the superficial laminas of the spinal cord dorsal horn after nerve section.

Authors:  David I Hughes; Dugald T Scott; Andrew J Todd; John S Riddell
Journal:  J Neurosci       Date:  2003-10-22       Impact factor: 6.167

3.  Distribution and injury-induced plasticity of cadherins in relationship to identified synaptic circuitry in adult rat spinal cord.

Authors:  John H Brock; Alice Elste; George W Huntley
Journal:  J Neurosci       Date:  2004-10-06       Impact factor: 6.167

4.  A novel method to quantify histochemical changes throughout the mediolateral axis of the substantia gelatinosa after spared nerve injury: characterization with TRPV1 and substance P.

Authors:  Gregory Corder; Andrew Siegel; Allison B Intondi; Xing Zhang; James E Zadina; Bradley K Taylor
Journal:  J Pain       Date:  2010-04       Impact factor: 5.820

5.  Choleragenoid horseradish peroxidase used for studying projections of some hindlimb cutaneous nerves and plantar foot afferents to the dorsal horn and Clarke's column in the rat.

Authors:  C Rivero-Melián; G Grant
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

6.  Stereological and somatotopic analysis of the spinal microglial response to peripheral nerve injury.

Authors:  Simon Beggs; Michael W Salter
Journal:  Brain Behav Immun       Date:  2006-12-16       Impact factor: 7.217

7.  Proper development of relay somatic sensory neurons and D2/D4 interneurons requires homeobox genes Rnx/Tlx-3 and Tlx-1.

Authors:  Ying Qian; Senji Shirasawa; Chih-Li Chen; Leping Cheng; Qiufu Ma
Journal:  Genes Dev       Date:  2002-05-15       Impact factor: 11.361

Review 8.  Neuronal circuitry for pain processing in the dorsal horn.

Authors:  Andrew J Todd
Journal:  Nat Rev Neurosci       Date:  2010-11-11       Impact factor: 34.870

9.  Peripheral nerve injury alters excitatory synaptic transmission in lamina II of the rat dorsal horn.

Authors:  Tatsuro Kohno; Kimberly A Moore; Hiroshi Baba; Clifford J Woolf
Journal:  J Physiol       Date:  2003-02-07       Impact factor: 5.182

10.  Innocuous, not noxious, input activates PKCgamma interneurons of the spinal dorsal horn via myelinated afferent fibers.

Authors:  Simona Neumann; Joao M Braz; Kate Skinner; Ida J Llewellyn-Smith; Allan I Basbaum
Journal:  J Neurosci       Date:  2008-08-06       Impact factor: 6.167

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