Literature DB >> 6643730

Anatomical and physiological studies of the gray matter surrounding the spinal cord central canal.

R L Nahin, A M Madsen, G J Giesler.   

Abstract

Recent histochemical evidence suggests that neurons in the gray matter surrounding the central canal may play a role in nociception. We attempted to evaluate this possibility by studying the response properties and ascending projections of these cells in the rat. In the first series of experiments, the ascending projections of neurons around the central canal were studied by the method of retrograde transport of horseradish peroxidase (HRP). Predominantly contralateral labeling of neurons around the central canal appeared after HRP injections into the paramedian medullary or pontine reticular formation in intact or cerebellectomized animals. Far fewer cells were labeled by injections into the lateral medulla and/or pons. A small number of cells was retrogradely labeled by HRP injections into the vermal and intermediate regions of the cerebellum or the periaqueductal gray matter. Injections into other brainstem areas outside of the reticular formation also failed to label large numbers of neurons around the centra canal. In a second set of experiments, we recorded extracellular unitary activity from the lumbar enlargement in spinalized, decerebrate, unanesthetized rats. Thirteen units were functionally characterized and histologically localized within 300 micrometers of the central canal. All of the units identified responded exclusively to noxious stimuli applied within highly circumscribed receptive fields. Thus, neurons around the central canal contribute strongly to long ascending spinal cord projections. Physiologically, neurons found within this region are reminiscent of the noxious-specific cells in the outer most layers of the dorsal horn.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6643730     DOI: 10.1002/cne.902200306

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


  20 in total

1.  Identification of the G-protein-coupled ORL1 receptor in the mouse spinal cord by [35S]-GTPgammaS binding and immunohistochemistry.

Authors:  M Narita; H Mizoguchi; D E Oji; N J Dun; B H Hwang; H Nagase; L F Tseng
Journal:  Br J Pharmacol       Date:  1999-11       Impact factor: 8.739

2.  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

3.  Upper thoracic postsynaptic dorsal column neurons conduct cardiac mechanoreceptive information, but not cardiac chemical nociception in rats.

Authors:  Melanie D Goodman-Keiser; Chao Qin; Ann M Thompson; Robert D Foreman
Journal:  Brain Res       Date:  2010-11-03       Impact factor: 3.252

4.  Localization of substance P-like immunoreactive fibers in the thoracic spinal cord of guinea pig.

Authors:  M S Davidoff; P G Galabov; P Kaufmann
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

5.  Phosphorylation of transcription factor CREB in rat spinal cord after formalin-induced hyperalgesia: relationship to c-fos induction.

Authors:  R R Ji; F Rupp
Journal:  J Neurosci       Date:  1997-03-01       Impact factor: 6.167

Review 6.  Structure-function relationships in identified afferent neurones.

Authors:  S Mense
Journal:  Anat Embryol (Berl)       Date:  1990

7.  Is there a pathway in the posterior funiculus that signals visceral pain?

Authors:  R M Hirshberg; E D Al-Chaer; N B Lawand; K N Westlund; W D Willis
Journal:  Pain       Date:  1996-10       Impact factor: 6.961

8.  Ependyma of the central canal of the rat spinal cord: a light and transmission electron microscopic study.

Authors:  J E Bruni; K Reddy
Journal:  J Anat       Date:  1987-06       Impact factor: 2.610

9.  Neuroprotective ferulic acid (FA)-glycol chitosan (GC) nanoparticles for functional restoration of traumatically injured spinal cord.

Authors:  Wei Wu; Seung-Young Lee; Xiangbing Wu; Jacqueline Y Tyler; He Wang; Zheng Ouyang; Kinam Park; Xiao-Ming Xu; Ji-Xin Cheng
Journal:  Biomaterials       Date:  2013-12-12       Impact factor: 12.479

10.  Spinal cord transection significantly influences nNOS-IR in neuronal circuitry that underlies the tail-flick reflex activity.

Authors:  Alexandra Dávidová; Andrea Schreiberová; Dalibor Kolesár; L'udmila Capková; Ol'ga Krizanová; Nadezda Lukácová
Journal:  Cell Mol Neurobiol       Date:  2009-03-17       Impact factor: 5.046

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.