Literature DB >> 3968229

The somatotopic organization of primary afferent terminals in the superficial laminae of the dorsal horn of the rat spinal cord.

J E Swett, C J Woolf.   

Abstract

Transganglionic transport of wheatgerm agglutinin conjugated horse-radish peroxidase (WGA-HRP) was used to reveal the central distribution of terminals of primary afferent fibers from peripheral nerves innervating the hind leg of the rat. In separate experiments the sizes and locations of cutaneous peripheral receptive fields were determined by electrophysiological recording techniques for each of the nerves that had been labeled with WGA-HRP. By using digital image analysis, the sizes and positions of the peripheral receptive fields were correlated with the areas of superficial dorsal horn occupied by terminals of primary afferents from each of these receptive fields. Data were obtained from the posterior cutaneous nerve of the thigh, lateral sural, sural, saphenous, superficial peroneal, and tibial nerves. The subdivisions of the sciatic nerve, the sural, lateral sural, superficial peroneal, and tibial nerves each projected to a separate and distinct region of the superficial dorsal horn and collectively formed a "U"-shaped zone of terminal labeling extending from lumbar spinal segments L2 to the caudal portions of L5. The gap in the "U" extended from L2 to the L3-4 boundary and was occupied by terminals from the saphenous nerve. Collectively, all primary afferents supplying the hindlimb occupied the medial 3/4 of the superficial dorsal horn with terminals from the tibial nerve lying most medially and occupying the largest of all the terminal fields. Afferents from the superficial peroneal lay in a zone between the medially situated tibial zone and the more laterally placed sural zone. Afferents from the posterior cutaneous nerve were located most caudally and laterally. Terminal fields from the posterior cutaneous and saphenous nerves differed from the others in having split representations caused presumably by their proximity to the mid-axial line of the limb. Comparisons between the peripheral and the central representations of each nerve revealed that 1 mm2 of surface area of the superficial dorsal horn serves approximately 600-900 mm2 of hairy skin and roughly 300 mm2 of glabrous skin. The vast majority of terminal labeling observed in the dorsal horn was found in the marginal layer and substantia gelatinosa, suggesting that small diameter afferents have an orderly somatotopic arrangement in which each portion of the skin surface is innervated by afferent fibers that terminate in preferred localities within the dorsal horn.

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Mesh:

Year:  1985        PMID: 3968229     DOI: 10.1002/cne.902310106

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


  74 in total

1.  Sciatic nerve injury in adult rats causes distinct changes in the central projections of sensory neurons expressing different glial cell line-derived neurotrophic factor family receptors.

Authors:  Janet R Keast; Shelley L Forrest; Peregrine B Osborne
Journal:  J Comp Neurol       Date:  2010-08-01       Impact factor: 3.215

2.  Spinal sensorimotor transformation: relation between cutaneous somatotopy and a reflex network.

Authors:  Anders Levinsson; Hans Holmberg; Jonas Broman; Mengliang Zhang; Jens Schouenborg
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

3.  Electrophysiological mapping of the nociceptive inputs to the substantia gelatinosa in rat horizontal spinal cord slices.

Authors:  Go Kato; Hidemasa Furue; Toshihiko Katafuchi; Toshiharu Yasaka; Yukihide Iwamoto; Megumu Yoshimura
Journal:  J Physiol       Date:  2004-08-05       Impact factor: 5.182

4.  Stance-phase force on the opposite limb dictates swing-phase afferent presynaptic inhibition during locomotion.

Authors:  Heather Brant Hayes; Young-Hui Chang; Shawn Hochman
Journal:  J Neurophysiol       Date:  2012-03-21       Impact factor: 2.714

5.  Sensory representation of the wing in the spinal dorsal horn of the pigeon.

Authors:  R Necker
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

6.  Time-related changes in the labeling pattern of motor and sensory neurons innervating the gastrocnemius muscle, as revealed by the retrograde transport of the cholera toxin B subunit.

Authors:  M Hirakawa; J T McCabe; M Kawata
Journal:  Cell Tissue Res       Date:  1992-03       Impact factor: 5.249

7.  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

8.  Effects of distal nerve injuries on dorsal-horn neurons and glia: relationships between lesion size and mechanical hyperalgesia.

Authors:  J W Lee; S M Siegel; A L Oaklander
Journal:  Neuroscience       Date:  2008-10-11       Impact factor: 3.590

Review 9.  Spatial organization of cortical and spinal neurons controlling motor behavior.

Authors:  Ariel J Levine; Kathryn A Lewallen; Samuel L Pfaff
Journal:  Curr Opin Neurobiol       Date:  2012-07-27       Impact factor: 6.627

10.  Functional electrical stimulation helps replenish progenitor cells in the injured spinal cord of adult rats.

Authors:  Daniel Becker; Devin S Gary; Ephron S Rosenzweig; Warren M Grill; John W McDonald
Journal:  Exp Neurol       Date:  2010-01-06       Impact factor: 5.330

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