Literature DB >> 109477

Spinal termination of functionally identified primary afferent neurons with slowly conducting myelinated fibers.

A R Light, E R Perl.   

Abstract

Single primary afferent myelinated fibers from cutaneous receptors of cat and monkey were functionally identified by recording from the spinal cord with micropipettes filled with horseradish peroxidase (HRP). Relatively slowly conducting fibers (less than 40 m/sec) from high threshold mechanoreceptors (mechanical nociceptors) and two types of low threshold mechanoreceptor (D-hair and field) were selected for staining. Iontophoresis of the HRP and subsequent histochemical reaction stained the axons recorded from and their collaterals, including terminations, for several millimeters. The termination patterns in the two species proved essentially identical. Ipsilaterally, the mechanical nociceptor fibers terminated principally in the dorsal horn's marginal zone and in the ventral parts of the nucleus proprius (lamina V in the cat). Some of these nociceptors also had terminals in the midline just dorsal to the central canal, contralaterally in the marginal zone, and at the base of the opposite nucleus proprius. In contrast, the D-hair primary afferent axons terminated in the dorsal part of the nucleus proprius overlapping into the innermost portion of the substantia gelatinosa. The field receptor fibers terminated predominantly in the middle part of the nucleus proprius. These results suggest that there is a highly specialized central projection of primary afferent endings which is related to sensory function and not to fiber diameter. The marginal zone and most dorsal parts of the substantia gelatinosa receive direct projections from cutaneous nociceptors but do not have direct input from cutaneous receptors transmitting activity initiated by innocuous stimulation.

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Year:  1979        PMID: 109477     DOI: 10.1002/cne.901860203

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


  113 in total

1.  Ascending projections from the area around the spinal cord central canal: A Phaseolus vulgaris leucoagglutinin study in rats.

Authors:  C C Wang; W D Willis; K N Westlund
Journal:  J Comp Neurol       Date:  1999-12-20       Impact factor: 3.215

2.  Widespread projections from myelinated nociceptors throughout the substantia gelatinosa provide novel insights into neonatal hypersensitivity.

Authors:  C Jeffery Woodbury; H Richard Koerber
Journal:  J Neurosci       Date:  2003-01-15       Impact factor: 6.167

3.  Spinal neurons exhibiting a specific nociceptive response receive abundant substance P-containing synaptic contacts.

Authors:  Y De Koninck; A Ribeiro-da-Silva; J L Henry; A C Cuello
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

4.  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

5.  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

6.  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

7.  Inflammation reduces the contribution of N-type calcium channels to primary afferent synaptic transmission onto NK1 receptor-positive lamina I neurons in the rat dorsal horn.

Authors:  Beth K Rycroft; Kristina S Vikman; MacDonald J Christie
Journal:  J Physiol       Date:  2007-02-15       Impact factor: 5.182

8.  Synaptic responses of substantia gelatinosa neurones to dorsal column stimulation in rat spinal cord in vitro.

Authors:  H Baba; M Yoshimura; S Nishi; K Shimoji
Journal:  J Physiol       Date:  1994-07-01       Impact factor: 5.182

9.  Distinct central representations for sensory fibers innervating either the conjunctiva or cornea of the rat.

Authors:  W Michael Panneton; Hugo Hsu; Qi Gan
Journal:  Exp Eye Res       Date:  2009-12-11       Impact factor: 3.467

10.  Post-tetanic depression of spinal reflexes in the rabbit and the possible involvement of opioid peptides.

Authors:  D M Catley; R W Clarke; J E Pascoe
Journal:  J Physiol       Date:  1984-07       Impact factor: 5.182

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