Literature DB >> 10375678

The types of neuron which contain protein kinase C gamma in rat spinal cord.

E Polgár1, J H Fowler, M M McGill, A J Todd.   

Abstract

Protein kinase C (PKC) is thought to have a role in sensitization of dorsal horn neurons in certain pain states, and a recent study has reported that mice which lack the gamma isoform (PKCgamma) show reduced neuropathic pain after peripheral nerve injury. Although PKCgamma is present at high levels in the ventral part of lamina II we have limited information concerning the types of neuron in which it is located. In this study we have used immunocytochemistry to characterise the neurons which contain PKCgamma. Immunoreactive neurons were concentrated in ventral lamina II, but were also present in lamina III. Some weakly-immunoreactive neurons were located in the dorsal part of lamina II and in lamina I. The great majority (92%) of cells with PKCgamma were not GABA-immunoreactive, and these cells are likely to be excitatory interneurons. Dual-immunofluorescence labelling showed that PKCgamma was not randomly distributed amongst non-GABAergic neurons, since it was present in 76% of cells with neurotensin and 45% of those with somatostatin, but only 5% of those with the mu-opioid receptor (MOR-1). Cells with the neurokinin 1 receptor are found in lamina I and lamina III, and PKCgamma was present in 22% and 37% of these populations, respectively. These results suggest that excitatory interneurons in laminae II and III which lack the micro-opioid receptor may have a significant role in generating neuropathic pain. Copyright 1999 Elsevier Science B.V.

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Year:  1999        PMID: 10375678     DOI: 10.1016/s0006-8993(99)01500-0

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  64 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-29       Impact factor: 11.205

2.  Involvement of spinal protein kinase Cgamma in the attenuation of opioid mu-receptor-mediated G-protein activation after chronic intrathecal administration of [D-Ala2,N-MePhe4,Gly-Ol(5)]enkephalin.

Authors:  M Narita; H Mizoguchi; M Narita; H Nagase; T Suzuki; L F Tseng
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3.  Pain processing by spinal microcircuits: afferent combinatorics.

Authors:  Steven A Prescott; Stéphanie Ratté
Journal:  Curr Opin Neurobiol       Date:  2012-03-10       Impact factor: 6.627

4.  Lack of evidence for sprouting of Abeta afferents into the superficial laminas of the spinal cord dorsal horn after nerve section.

Authors:  David I Hughes; Dugald T Scott; Andrew J Todd; John S Riddell
Journal:  J Neurosci       Date:  2003-10-22       Impact factor: 6.167

5.  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

6.  Ontogeny of excitatory spinal neurons processing distinct somatic sensory modalities.

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Journal:  J Neurosci       Date:  2013-09-11       Impact factor: 6.167

7.  Spinal mediators that may contribute selectively to antinociceptive tolerance but not other effects of morphine as revealed by deletion of GluR5.

Authors:  A M Gregus; C N Inra; T P Giordano; A C S Costa; A M Rajadhyaksha; C E Inturrisi
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Review 8.  Spinal and afferent PKC signaling mechanisms that mediate chronic pain in sickle cell disease.

Authors:  Ying He; Zaijie Jim Wang
Journal:  Neurosci Lett       Date:  2019-04-30       Impact factor: 3.046

Review 9.  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

10.  5-HT2A Receptor-Induced Morphological Reorganization of PKCγ-Expressing Interneurons Gates Inflammatory Mechanical Allodynia in Rat.

Authors:  Cristina Alba-Delgado; Sarah Mountadem; Noémie Mermet-Joret; Lénaïc Monconduit; Radhouane Dallel; Alain Artola; Myriam Antri
Journal:  J Neurosci       Date:  2018-10-24       Impact factor: 6.167

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