Literature DB >> 17717012

Morphology of inhibitory and excitatory interneurons in superficial laminae of the rat dorsal horn.

David J Maxwell1, Mino D Belle, Ornsiri Cheunsuang, Anika Stewart, Richard Morris.   

Abstract

If we are to stand any chance of understanding the circuitry of the superficial dorsal horn, it is imperative that we can identify which classes of interneuron are excitatory and which are inhibitory. Our aim was to test the hypothesis that there is a correlation between the morphology of an interneuron and its postsynaptic action. We used in vitro slice preparations of the rat spinal cord to characterize and label interneurons in laminae I-III with Neurobiotin. Labelled cells (n = 19) were reconstructed in 3D with Neurolucida and classified according to the scheme proposed by Grudt & Perl (2002). We determined if cells were inhibitory or excitatory by reacting their axon terminals with antibodies to reveal glutamate decrboxylase (for GABAergic cells) or the vesicular glutamate transporter 2 (for glutamatergic cells). All five islet cells retrieved were inhibitory. Of the six vertical (stalked) cells analysed, four were excitatory and, surprisingly, two were inhibitory. It was noted that these inhibitory cells had axonal projections confined to lamina II whereas excitatory vertical cells projected to lamina I and II. Of the remaining neurons, three were radial cells (2 inhibitory, 1 excitatory), two were antennae cells (1 inhibitory, 1 excitatory), one was an inhibitory central cell and the remaining two were unclassifiable excitatory cells. Our hypothesis appears to be correct only for islet cells. Other classes of cells have mixed actions, and in the case of vertical cells, the axonal projection appears to be a more important determinant of postsynaptic action.

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Year:  2007        PMID: 17717012      PMCID: PMC2277171          DOI: 10.1113/jphysiol.2007.140996

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  23 in total

1.  Spinal lamina I neurons that express neurokinin 1 receptors: morphological analysis.

Authors:  O Cheunsuang; R Morris
Journal:  Neuroscience       Date:  2000       Impact factor: 3.590

2.  Immunocytochemical localization of glutamic acid decarboxylase in physiologically identified interneurons of hamster spinal laminae III-V.

Authors:  S P Schneider; M Lopez
Journal:  Neuroscience       Date:  2002       Impact factor: 3.590

3.  Morphological and physiological features of a set of spinal substantia gelatinosa neurons defined by green fluorescent protein expression.

Authors:  Adam W Hantman; Anthony N van den Pol; Edward R Perl
Journal:  J Neurosci       Date:  2004-01-28       Impact factor: 6.167

4.  The expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in neurochemically defined axonal populations in the rat spinal cord with emphasis on the dorsal horn.

Authors:  A J Todd; D I Hughes; E Polgár; G G Nagy; M Mackie; O P Ottersen; D J Maxwell
Journal:  Eur J Neurosci       Date:  2003-01       Impact factor: 3.386

5.  Cell-type-specific excitatory and inhibitory circuits involving primary afferents in the substantia gelatinosa of the rat spinal dorsal horn in vitro.

Authors:  Toshiharu Yasaka; Go Kato; Hidemasa Furue; Md Harunor Rashid; Motoki Sonohata; Akihiro Tamae; Yuzo Murata; Sadahiko Masuko; Megumu Yoshimura
Journal:  J Physiol       Date:  2007-03-08       Impact factor: 5.182

6.  The large synaptic complexes of the substantia gelatinosa.

Authors:  M Réthelyi; J Szentágothai
Journal:  Exp Brain Res       Date:  1969       Impact factor: 1.972

7.  Golgi studies of the neurons in layer II of the dorsal horn of the medulla (trigeminal nucleus caudalis).

Authors:  S Gobel
Journal:  J Comp Neurol       Date:  1978-07-15       Impact factor: 3.215

8.  Golgi studies in the substantia gelatinosa neurons in the spinal trigeminal nucleus.

Authors:  S Gobel
Journal:  J Comp Neurol       Date:  1975-08-01       Impact factor: 3.215

9.  Distribution and colocalisation of glutamate decarboxylase isoforms in the rat spinal cord.

Authors:  M Mackie; D I Hughes; D J Maxwell; N J K Tillakaratne; A J Todd
Journal:  Neuroscience       Date:  2003       Impact factor: 3.590

Review 10.  Spinal dorsal horn neurone targets for nociceptive primary afferents: do single neurone morphological characteristics suggest how nociceptive information is processed at the spinal level.

Authors:  Richard Morris; Ornsiri Cheunsuang; Anika Stewart; David Maxwell
Journal:  Brain Res Brain Res Rev       Date:  2004-10
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  66 in total

1.  Inhibitory neurones of the spinal substantia gelatinosa mediate interaction of signals from primary afferents.

Authors:  Jihong Zheng; Yan Lu; Edward R Perl
Journal:  J Physiol       Date:  2010-04-19       Impact factor: 5.182

2.  Transcript expression of vesicular glutamate transporters in lumbar dorsal root ganglia and the spinal cord of mice - effects of peripheral axotomy or hindpaw inflammation.

Authors:  M Malet; C A Vieytes; K H Lundgren; R P Seal; E Tomasella; K B Seroogy; T Hökfelt; G F Gebhart; P R Brumovsky
Journal:  Neuroscience       Date:  2013-05-31       Impact factor: 3.590

3.  Three-dimensional organization of local excitatory and inhibitory inputs to neurons in laminae III-IV of the spinal dorsal horn.

Authors:  Go Kato; Masafumi Kosugi; Masaharu Mizuno; Andrew M Strassman
Journal:  J Physiol       Date:  2013-08-27       Impact factor: 5.182

Review 4.  Ionotropic glutamate receptors in spinal nociceptive processing.

Authors:  Max Larsson
Journal:  Mol Neurobiol       Date:  2009-10-31       Impact factor: 5.590

Review 5.  Transmitting pain and itch messages: a contemporary view of the spinal cord circuits that generate gate control.

Authors:  João Braz; Carlos Solorzano; Xidao Wang; Allan I Basbaum
Journal:  Neuron       Date:  2014-05-07       Impact factor: 17.173

6.  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

7.  Large projection neurons in lamina I of the rat spinal cord that lack the neurokinin 1 receptor are densely innervated by VGLUT2-containing axons and possess GluR4-containing AMPA receptors.

Authors:  Erika Polgár; Khulood M Al-Khater; Safa Shehab; Masahiko Watanabe; Andrew J Todd
Journal:  J Neurosci       Date:  2008-12-03       Impact factor: 6.167

8.  Neurokinin 1 receptor-expressing projection neurons in laminae III and IV of the rat spinal cord have synaptic AMPA receptors that contain GluR2, GluR3 and GluR4 subunits.

Authors:  Andrew J Todd; Erika Polgár; Christine Watt; Mark E S Bailey; Masahiko Watanabe
Journal:  Eur J Neurosci       Date:  2009-02-06       Impact factor: 3.386

9.  Antinociceptive action of oxytocin involves inhibition of potassium channel currents in lamina II neurons of the rat spinal cord.

Authors:  Jean Didier Breton; Pierrick Poisbeau; Pascal Darbon
Journal:  Mol Pain       Date:  2009-11-12       Impact factor: 3.395

10.  Quantitative characterization of low-threshold mechanoreceptor inputs to lamina I spinoparabrachial neurons in the rat.

Authors:  David Andrew
Journal:  J Physiol       Date:  2009-11-23       Impact factor: 5.182

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