Literature DB >> 9067842

Spatial distribution of kainate receptor subunit mRNA in the mouse basal ganglia and ventral mesencephalon.

S Bischoff1, J Barhanin, B Bettler, C Mulle, S Heinemann.   

Abstract

In an attempt to gain knowledge of the possible functions of kainate receptors, we have used in situ hybridization to examine the regional and cellular expression patterns of glutamate receptor subunits GluR5-7, KA1 and KA2 in the adult mouse basal ganglia, known to play a pivotal role in the translation of motivation into actions. Kainate receptor subunits were found to be differentially expressed in the circuitry forming the basal ganglia. They differ from each other in expression levels and their spatial localization. GluR6 appeared as the key subunit for the descending gamma-aminobutyric acid (GABA)ergic-glutamatergic pathways, with highest message levels in the caudate putamen, globus pallidus and subthalamic nucleus as well as in the nucleus accumbens and olfactory tubercle. GluR7 exhibited highest expression in the ascending nigrostriatal and mesolimbic dopaminergic neurons. GluR5 had a restricted distribution pattern, with high expression in the ventral pallidum, the islands of Calleja and pars compacta of the substantia nigra. KA2 was usually coexpressed with GluR6, although with a generally lower level of expression. Finally, KA1 mRNA was barely detectable in these neuronal circuits. These data suggest that kainate receptors in general may be involved in the functions associated with the basal ganglia, with a key role in the control of the central dopaminergic transmission. Thus, they might be implicated in the neurodegenerative and psychic disorders associated with an impairment of the basal ganglia.

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Year:  1997        PMID: 9067842     DOI: 10.1002/(sici)1096-9861(19970324)379:4<541::aid-cne6>3.0.co;2-2

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


  22 in total

1.  Functional GluR6 kainate receptors in the striatum: indirect downregulation of synaptic transmission.

Authors:  K Chergui; A Bouron; E Normand; C Mulle
Journal:  J Neurosci       Date:  2000-03-15       Impact factor: 6.167

2.  Activation of presynaptic kainate receptors suppresses GABAergic synaptic transmission in the rat globus pallidus.

Authors:  X-T Jin; Y Smith
Journal:  Neuroscience       Date:  2007-07-20       Impact factor: 3.590

3.  Contrary roles of kainate receptors in transmitter release at corticothalamic synapses onto thalamic relay and reticular neurons.

Authors:  Mariko Miyata; Keiji Imoto
Journal:  J Physiol       Date:  2009-01-05       Impact factor: 5.182

4.  Molecular components of striatal plasticity: the various routes of cyclic AMP pathways.

Authors:  A Rajadhyaksha; J Leveque; W Macías; A Barczak; C Konradi
Journal:  Dev Neurosci       Date:  1998       Impact factor: 2.984

Review 5.  Localization and functions of kainate receptors in the basal ganglia.

Authors:  Xiao-Tao Jin; Yoland Smith
Journal:  Adv Exp Med Biol       Date:  2011       Impact factor: 2.622

6.  In Vitro Differentiation of Human Neural Progenitor Cells Into Striatal GABAergic Neurons.

Authors:  Lin Lin; Juan Yuan; Bjoern Sander; Monika M Golas
Journal:  Stem Cells Transl Med       Date:  2015-05-13       Impact factor: 6.940

7.  Heteromeric kainate receptors formed by the coassembly of GluR5, GluR6, and GluR7.

Authors:  C Cui; M L Mayer
Journal:  J Neurosci       Date:  1999-10-01       Impact factor: 6.167

8.  Deletion of the glutamate receptor 5 subunit of kainate receptors affects the development of morphine tolerance.

Authors:  Johanna J Bogulavsky; Ann M Gregus; Paul T-H Kim; Alberto C S Costa; Anjali M Rajadhyaksha; Charles E Inturrisi
Journal:  J Pharmacol Exp Ther       Date:  2008-10-28       Impact factor: 4.030

9.  Kainate receptor-mediated responses in the CA1 field of wild-type and GluR6-deficient mice.

Authors:  I Bureau; S Bischoff; S F Heinemann; C Mulle
Journal:  J Neurosci       Date:  1999-01-15       Impact factor: 6.167

10.  Identification of domains and amino acids involved in GLuR7 ion channel function.

Authors:  N Strutz; C Villmann; A Thalhammer; P Kizelsztein; M Eisenstein; V I Teichberg; M Hollmann
Journal:  J Neurosci       Date:  2001-01-15       Impact factor: 6.167

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