Literature DB >> 1702117

Analysis of calcitonin gene-related peptide-like immunoreactivity in the cat dorsal spinal cord and dorsal root ganglia provide evidence for a multisegmental projection of nociceptive C-fiber primary afferents.

R J Traub1, B Allen, E Humphrey, M A Ruda.   

Abstract

Recent studies have suggested that calcitonin gene-related peptide (CGRP) can be used as a marker for a subpopulation of nociceptive primary afferents. Consequently, CGRP-immunoreactive (CGRP-IR) primary afferents have been reported to project many segments rostral to their segment of entry and to send collaterals into the superficial and deep laminae of the dorsal horn. This study reports that some CGRP-IR primary afferents of sacral origin project rostral through the ipsilateral lumbar enlargement in the cat. The ultrastructure of these multisegmentally projecting primary afferent axons and terminals identified in a partially denervated cat was examined and compared to the ultrastructure of CGRP-IR afferents from an intact cat. Retrograde transport of wheatgerm agglutinin-colloidal gold injected into the cat L4 spinal cord resulted in labeling of primary afferent cell bodies in the ipsilateral L4-S1 dorsal root ganglia (DRG). Analysis of every fourth section through the ipsilateral S1 DRG revealed as many as 1,000 retrogradely labeled neuronal cell bodies. One third of these cell bodies were double labeled for CGRP-like immunoreactivity. The number of single- and double-labeled cells increased in ganglia closer to the injection site (L4-L7). At the ultrastructural level, in the lumbosacral dorsal spinal cord of a normal cat, most CGRP-IR axons were unmyelinated, while the rest were small myelinated axons. In both the superficial dorsal horn and lamina V, CGRP-IR varicosities were dome shaped, scallop shaped, or elongated. The CGRP-IR varicosities contained small agranular vesicles and frequently a few dense core vesicles. These labeled varicosities formed asymmetric synapses on unlabeled dendritic spines, shafts, or neuronal somata. One cat received multiple unilateral dorsal rhizotomies (S1-L4) and an ipsilateral hemisection (mid L4). CGRP-IR axons and terminals were found within each of the rhizotomized segments, although their density was greatly reduced compared to that in the intact animals. In Lissauer's tract the majority (greater than 90%) of CGRP-IR fibers were unmyelinated. In laminae I and V, the remaining CGRP-IR varicosities were mainly the dome-shaped varicosities morphologically similar to those observed in the normal spinal cords. They contained small agranular vesicles and a few dense core vesicles and formed asymmetric synapses on unlabeled dendritic shafts and spines. These data demonstrate that unmyelinated, presumably C-fiber nociceptive primary afferents and some small myelinated A-delta nociceptive primary afferents of sacral origin project rostral through the cat lumbar enlargement and make synaptic connections in both the superficial and deep laminae of the cat dorsal spinal cord.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1702117     DOI: 10.1002/cne.903020312

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


  11 in total

1.  Spinal cord injury triggers an intrinsic growth-promoting state in nociceptors.

Authors:  Supinder S Bedi; Michael T Lago; Luke I Masha; Robyn J Crook; Raymond J Grill; Edgar T Walters
Journal:  J Neurotrauma       Date:  2011-11-04       Impact factor: 5.269

2.  Electrophysiological characterization of vagal afferents relevant to mucosal nociception in the rat upper oesophagus.

Authors:  J K M Lennerz; C Dentsch; N Bernardini; T Hummel; W L Neuhuber; P W Reeh
Journal:  J Physiol       Date:  2007-05-03       Impact factor: 5.182

3.  Chronic spontaneous activity generated in the somata of primary nociceptors is associated with pain-related behavior after spinal cord injury.

Authors:  Supinder S Bedi; Qing Yang; Robyn J Crook; Junhui Du; Zizhen Wu; Harvey M Fishman; Raymond J Grill; Susan M Carlton; Edgar T Walters
Journal:  J Neurosci       Date:  2010-11-03       Impact factor: 6.167

4.  Prenatal expression of purinergic receptor P2X3 in human dorsal root ganglion.

Authors:  Aihua Pan; Haiping Wu; Ming Li; Dahua Lu; Xu He; Xinan Yi; Xiao-Xin Yan; Zhiyuan Li
Journal:  Purinergic Signal       Date:  2011-11-04       Impact factor: 3.765

5.  Collateral projections of trigeminal ganglion neurons to both the principal sensory trigeminal and the spinal trigeminal nuclei in the rat.

Authors:  Y Q Li; M Takada; H Ohishi; Y Shinonaga; N Mizuno
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

Review 6.  Cutaneous neuroma physiology and its relationship to chronic pain.

Authors:  Catherine Curtin; Ian Carroll
Journal:  J Hand Surg Am       Date:  2009-05-28       Impact factor: 2.230

7.  Nociceptors as chronic drivers of pain and hyperreflexia after spinal cord injury: an adaptive-maladaptive hyperfunctional state hypothesis.

Authors:  Edgar T Walters
Journal:  Front Physiol       Date:  2012-08-02       Impact factor: 4.566

8.  Localization of Brain Natriuretic Peptide Immunoreactivity in Rat Spinal Cord.

Authors:  Essam M Abdelalim; Jean-Pierre Bellier; Ikuo Tooyama
Journal:  Front Neuroanat       Date:  2016-12-02       Impact factor: 3.856

9.  Nitric oxide-producing islet cells modulate the release of sensory neuropeptides in the rat substantia gelatinosa.

Authors:  P Aimar; L Pasti; G Carmignoto; A Merighi
Journal:  J Neurosci       Date:  1998-12-15       Impact factor: 6.167

10.  Resiniferatoxin for Pain Treatment: An Interventional Approach to Personalized Pain Medicine.

Authors:  Michael J Iadarola; Gian Luigi Gonnella
Journal:  Open Pain J       Date:  2013-03-08
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.