Literature DB >> 12589919

Role of kainate receptors in nociception.

Ruth Ruscheweyh1, Jürgen Sandkühler.   

Abstract

Nociceptive nerve fibers use L-glutamate as a fast excitatory neurotransmitter and it is therefore not surprising that both, ionotropic and metabotropic glutamate receptors play pivotal roles for transmission of nociceptive information in spinal cord. A subtype of ionotropic glutamate receptors, the kainate receptor, is present in spinal dorsal horn. However, its role has remained obscure as specific antagonists and agonists have become available only recently. Kainate receptors are present on small, including nociceptive, dorsal root ganglion cells and on intrinsic dorsal horn neurons, and those two locations can be targeted separately by appropriate agonists and antagonists. Postsynaptic kainate receptors on spinal dorsal horn neurons are activated by high intensity electrical stimulation of the dorsal root entry zone that activates nociceptive primary afferent fibers. In contrast, low intensity stimulation that activates only non-nociceptive fibers is ineffective. Selective blockade of kainate receptors may produce analgesia. Here, we review what is known about localization of kainate receptors in dorsal root ganglia and spinal dorsal horn and their physiological and pathophysiological importance with special reference to nociceptive pathways. A short overview on molecular biology and agonist and antagonist pharmacology is included.

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Year:  2002        PMID: 12589919     DOI: 10.1016/s0165-0173(02)00203-5

Source DB:  PubMed          Journal:  Brain Res Brain Res Rev


  12 in total

1.  Kainate receptors are primarily postsynaptic to SP-containing axon terminals in the trigeminal dorsal horn.

Authors:  Deborah M Hegarty; Jennifer L Mitchell; Kristin C Swanson; Sue A Aicher
Journal:  Brain Res       Date:  2007-10-04       Impact factor: 3.252

Review 2.  Neuroplasticity of ascending and descending pathways after somatosensory system injury: reviewing knowledge to identify neuropathic pain therapeutic targets.

Authors:  P Boadas-Vaello; S Castany; J Homs; B Álvarez-Pérez; M Deulofeu; E Verdú
Journal:  Spinal Cord       Date:  2016-01-12       Impact factor: 2.772

3.  Regioselective Domino Metathesis of Unsymmetrical 7-Oxanorbornenes with Electron-Rich Vinyl Acetate toward Biologically Active Glutamate Analogues.

Authors:  Masato Oikawa; Minoru Ikoma; Makoto Sasaki; Martin B Gill; Geoffrey T Swanson; Keiko Shimamoto; Ryuichi Sakai
Journal:  European J Org Chem       Date:  2009-11-01

Review 4.  Spinal cord mechanisms of chronic pain and clinical implications.

Authors:  Hsinlin Thomas Cheng
Journal:  Curr Pain Headache Rep       Date:  2010-06

5.  Modulation of excitatory synaptic transmission in the spinal substantia gelatinosa of mice deficient in the kainate receptor GluR5 and/or GluR6 subunit.

Authors:  Dong-Ho Youn; Mirjana Randic
Journal:  J Physiol       Date:  2004-01-14       Impact factor: 5.182

6.  Regioselective Domino Metathesis of 7-Oxanorbornenes and Its Application to the Synthesis of Biologically Active Glutamate Analogues.

Authors:  Minoru Ikoma; Masato Oikawa; Martin B Gill; Geoffrey T Swanson; Ryuichi Sakai; Keiko Shimamoto; Makoto Sasaki
Journal:  European J Org Chem       Date:  2008-11

7.  Activation of iGluR5 kainate receptors inhibits neurogenic dural vasodilatation in an animal model of trigeminovascular activation.

Authors:  A P Andreou; P R Holland; P J Goadsby
Journal:  Br J Pharmacol       Date:  2009-03-20       Impact factor: 8.739

8.  Molecular and pharmacological evidence for a facilitatory functional role of pre-synaptic GLUK2/3 kainate receptors on GABA release in rat trigeminal caudal nucleus.

Authors:  I Samengo; D Currò; P Navarra; V Barrese; M Taglialatela; M Martire
Journal:  Eur J Pain       Date:  2012-03-06       Impact factor: 3.931

9.  Modulation of nociceptive dural input to the trigeminocervical complex through GluK1 kainate receptors.

Authors:  Anna P Andreou; Philip R Holland; Michele P Lasalandra; Peter J Goadsby
Journal:  Pain       Date:  2015-03       Impact factor: 7.926

10.  A Targeted Mutation Disrupting Mitochondrial Complex IV Function in Primary Afferent Neurons Leads to Pain Hypersensitivity Through P2Y1 Receptor Activation.

Authors:  Rory Mitchell; Graham Campbell; Marta Mikolajczak; Katie McGill; Don Mahad; Sue M Fleetwood-Walker
Journal:  Mol Neurobiol       Date:  2019-01-28       Impact factor: 5.590

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