Literature DB >> 6890076

Two types of synaptic glomeruli and their distribution in laminae I-III of the rat spinal cord.

A Ribeiro-da-Silva, A Coimbra.   

Abstract

Systematic examination of photomontages revealed two types of synaptic glomeruli in laminae II-III. Type I glomeruli have a dark small central (C) terminal of indented contour with closely packed spherical vesicles of variable diameter and few mitochondria. Among the peripheral terminals there are dendritic spines and a few presynaptic dendritic spines (V1 terminals) and axon endings rich in discoid vesicles (V2). These glomeruli occur in groups which are particularly evident in parasagittal sections in which successive C terminals are connected by narrower portions or dark unmyelinated profiles. Type II glomeruli have an electron-lucent and large C terminal of regular contour with less packed synaptic vesicles of more uniform diameter, more mitochondria, and sometimes neurofilaments. Presynaptic dendrites are fewer and axon endings more numerous. C terminals in type II glomeruli are fusiform in longitudinal section, rarely occurring in groups. Lamina I is virtually devoid of glomeruli. Within lamina II, glomeruli are rare in the dorsalmost 20-micrometers band and abundant in the immediately ventral 20-micrometers band in which type I glomeruli are prevalent (approximately 79%). In ventral lamina II, type II glomeruli predominate (66%), being practically exclusive in lamina III where most contain neurofilaments. Considering the distribution of terminations of primary afferents, it is suggested that type I C terminals originated from unmyelinated primary afferents, type II C terminals without neurofilaments from direct myelinated fibers, the those with neurofilaments from recurrent large fibers. The distinct numbers of presynaptic dendritic and axonal endings suggest different modulatory mechanisms functioning in the two types and in ventral vs. dorsal areas of this region.

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Year:  1982        PMID: 6890076     DOI: 10.1002/cne.902090205

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


  40 in total

1.  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

2.  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

3.  AMPA receptor subunits underlying terminals of fine-caliber primary afferent fibers.

Authors:  A Popratiloff; R J Weinberg; A Rustioni
Journal:  J Neurosci       Date:  1996-05-15       Impact factor: 6.167

4.  Inhibitory Interneurons That Express GFP in the PrP-GFP Mouse Spinal Cord Are Morphologically Heterogeneous, Innervated by Several Classes of Primary Afferent and Include Lamina I Projection Neurons among Their Postsynaptic Targets.

Authors:  Robert P Ganley; Noboru Iwagaki; Patricia del Rio; Najma Baseer; Allen C Dickie; Kieran A Boyle; Erika Polgár; Masahiko Watanabe; Victoria E Abraira; Amanda Zimmerman; John S Riddell; Andrew J Todd
Journal:  J Neurosci       Date:  2015-05-13       Impact factor: 6.167

5.  The morphology of Golgi-stained neurons in lamina II of the rat spinal cord.

Authors:  A J Todd; S G Lewis
Journal:  J Anat       Date:  1986-12       Impact factor: 2.610

6.  Early morphological changes of primary afferent neurons and their processes in newborn mice after treatment with capsaicin.

Authors:  A Hiura; H Ishizuka
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

7.  The neuronal population of the marginal zone (lamina I) of the rat spinal cord. A study based on reconstructions of serially sectioned cells.

Authors:  D Lima; A Coimbra
Journal:  Anat Embryol (Berl)       Date:  1983

8.  The effects of cholinoceptor agonists and antagonists on C-fibre evoked responses in the substantia gelatinosa of neonatal rat spinal cord slices.

Authors:  L Bleazard; R Morris
Journal:  Br J Pharmacol       Date:  1993-11       Impact factor: 8.739

9.  Molecular architecture of endocannabinoid signaling at nociceptive synapses mediating analgesia.

Authors:  Rita Nyilas; Laura C Gregg; Ken Mackie; Masahiko Watanabe; Andreas Zimmer; Andrea G Hohmann; István Katona
Journal:  Eur J Neurosci       Date:  2009-05-09       Impact factor: 3.386

10.  A population of large neurons in laminae III and IV of the rat spinal cord that have long dorsal dendrites and lack the neurokinin 1 receptor.

Authors:  Erika Polgár; Suzanne Thomson; David J Maxwell; Khulood Al-Khater; Andrew J Todd
Journal:  Eur J Neurosci       Date:  2007-09       Impact factor: 3.386

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