Expression of glutamate receptors in the human and rat basal ganglia: Effect of the dopaminergic denervation on AMPA receptor gene expression in the striatopallidal complex in parkinson's disease and rat with 6‐OHDA lesion

The overactivity of subthalamopallidal and corticostriatal glutamatergic neurons observed in Parkinson's disease (PD) suggests that antagonists of glutamate receptor could be used to alleviate the motor symptoms of the disease. In this study, we analysed two features of the striatopallidal complex: (1) the distribution of α‐amino‐3 hydroxy‐5‐methyl‐4‐isoxasol‐propionate (AMPA) and kainate receptors and their corresponding mRNA by immunohistochemistry and in situ hybridisation and (2) the effect of dopaminergic denervation on AMPA receptor gene expression in PD patients and rats with 6‐hydroxydopamine (6‐OHDA)‐induced degeneration of the nigrostriatal dopaminergic system.

[1]  M. Starr Glutamate/dopamine D1/D2 balance in the basal ganglia and its relevance to Parkinson' disease , 1995, Synapse.

[2]  J. Greenamyre,et al.  Polysynaptic regulation of glutamate receptors and mitochondrial enzyme activities in the basal ganglia of rats with unilateral dopamine depletion , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[3]  R. Albin,et al.  Localization of ampa-selective excitatory amino acid receptor subunits in identified populations of striatal neurons , 1994, Neuroscience.

[4]  G. Godeheu,et al.  NMDA and carbachol but not AMPA affect differently the release of [3H]GABA in striosome- and matrix-enriched areas of the rat striatum , 1994, Brain Research.

[5]  J. Penney,et al.  Glutamate receptors in striatum and substantia nigra: Effects of medial forebrain bundle lesions , 1994, Brain Research.

[6]  D. Schoepp,et al.  Molecular Cloning, Expression, and Pharmacological Characterization of humEAA1, a Human Kainate Receptor Subunit , 1994, Journal of neurochemistry.

[7]  D. Calne,et al.  Treatment of Parkinson's disease. , 1993, The New England journal of medicine.

[8]  W Wisden,et al.  A complex mosaic of high-affinity kainate receptors in rat brain , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  J. Morrison,et al.  Quantitative localization of AMPA/kainate and kainate glutamate receptor subunit immunoreactivity in neurochemically identified subpopulations of neurons in the prefrontal cortex of the macaque monkey , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  R. Huganir,et al.  AMPA glutamate receptor subunits are differentially distributed in rat brain , 1993, Neuroscience.

[11]  L. Raymond,et al.  Phosphorylation and modulation of recombinant GluR6 glutamate receptors by cAMP-dependent protein kinase , 1993, Nature.

[12]  M. Tohyama,et al.  The differential expression patterns of messenger RNAs encoding non-N-methyl-d-aspartate glutamate receptor subunits (GluR1–4) in the rat brain , 1993, Neuroscience.

[13]  D. Price,et al.  The striatal mosaic in primates: striosomes and matrix are differentially enriched in ionotropic glutamate receptor subunits , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  André Parent,et al.  Differential patterns of arborization of striatal and subthalamic fibers in the two pallidal segments in primates , 1992, Brain Research.

[15]  Y. Agid,et al.  The glutamate antagonist, MK-801, does not prevent dopaminergic cell death induced by the 1-methyl-4-phenylpyridinium ion (MPP+) in rat dissociated mesencephalic cultures , 1992, Brain Research.

[16]  B. Bloch,et al.  Phenotypical characterization of the rat striatal neurons expressing muscarinic receptor genes , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[17]  J. Penney,et al.  Compartmentalization of excitatory amino acid receptors in human striatum. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Bert Sakmann,et al.  Heteromeric NMDA Receptors: Molecular and Functional Distinction of Subtypes , 1992, Science.

[19]  B. Sakmann,et al.  The KA-2 subunit of excitatory amino acid receptors shows widespread expression in brain and forms ion channels with distantly related subunits , 1992, Neuron.

[20]  R. Albin,et al.  Alternative excitotoxic hypotheses , 1992, Neurology.

[21]  A. F. Schinder,et al.  Molecular cloning, chromosomal mapping, and functional expression of human brain glutamate receptors. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[22]  C. Stevens,et al.  Cloning of a putative glutamate receptor: A low affinity kainate-binding subunit , 1992, Neuron.

[23]  J. Penney,et al.  Excitatory amino acid binding sites in the basal ganglia of the rat: A quantitative autoradiographic study , 1992, Neuroscience.

[24]  R. Wenthold,et al.  Immunochemical characterization of the non-NMDA glutamate receptor using subunit-specific antibodies. Evidence for a hetero-oligomeric structure in rat brain. , 1992, The Journal of biological chemistry.

[25]  C. Marescaux,et al.  Contralateral disappearance of parkinsonian signs after subthalamic hematoma , 1992, Neurology.

[26]  T. Klockgether,et al.  The AMPA receptor antagonist NBQX has antiparkinsonian effects in monoamine‐depleted rats and MPTP‐treated monkeys , 1991, Annals of neurology.

[27]  S. Heinemann,et al.  Cloning of a cDNA for a glutamate receptor subunit activated by kainate but not AMPA , 1991, Nature.

[28]  P. Seeburg,et al.  Cloning of a putative high-affinity kainate receptor expressed predominantly in hippocampal CA3 cells , 1991, Nature.

[29]  B. Bloch,et al.  Phenotypical characterization of the rat striatal neurons expressing the D1 dopamine receptor gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[30]  S. Heinemann,et al.  Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition , 1991, Science.

[31]  A. Gobert,et al.  The glutamate-mediated release of dopamine in the rat striatum: Further characterization of the dual excitatory-inhibitory function , 1990, Neuroscience.

[32]  C. Gerfen,et al.  D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. , 1990, Science.

[33]  S. Heinemann,et al.  Cloning of a novel glutamate receptor subunit, GluR5: Expression in the nervous system during development , 1990, Neuron.

[34]  T. Klockgether,et al.  NMDA antagonists potentiate antiparkinsonian actions of L‐dopa in monoamine‐depleted rats , 1990, Annals of neurology.

[35]  B. Sakmann,et al.  Flip and flop: a cell-specific functional switch in glutamate-operated channels of the CNS. , 1990, Science.

[36]  H. Bergman,et al.  Reversal of experimental parkinsonism by lesions of the subthalamic nucleus. , 1990, Science.

[37]  S. Heinemann,et al.  Molecular cloning and functional expression of glutamate receptor subunit genes. , 1990, Science.

[38]  B. Sakmann,et al.  A family of AMPA-selective glutamate receptors. , 1990, Science.

[39]  G. E. Alexander,et al.  Functional architecture of basal ganglia circuits: neural substrates of parallel processing , 1990, Trends in Neurosciences.

[40]  J. Penney,et al.  The functional anatomy of basal ganglia disorders , 1989, Trends in Neurosciences.

[41]  S. Heinemann,et al.  Cloning by functional expression of a member of the glutamate receptor family , 1989, Nature.

[42]  A. Graybiel,et al.  Melanized dopaminergic neurons are differentially susceptible to degeneration in Parkinson's disease , 1988, Nature.

[43]  A. D. Smith,et al.  Identification of synaptic terminals of thalamic or cortical origin in contact with distinct medium‐size spiny neurons in the rat neostriatum , 1988, The Journal of comparative neurology.

[44]  T. van Groen,et al.  Species differences in hippocampal commissural connections: Studies in rat, guinea pig, rabbit, and cat , 1988, The Journal of comparative neurology.

[45]  A. Parent,et al.  The striatopallidal and striatonigral projections: two distinct fiber systems in primate , 1984, Brain Research.

[46]  D L Price,et al.  Basal forebrain neurons in the dementia of Parkinson disease , 1983, Annals of neurology.

[47]  B. Scatton,et al.  N-methyl-D-aspartate-type receptors mediate striatal 3H-acetylcholine release evoked by excitatory amino acids , 1982, Nature.

[48]  Seymour Geisser,et al.  Statistical Principles in Experimental Design , 1963 .

[49]  S. Nakanishi,et al.  Molecular diversity and functions of glutamate receptors. , 1994, Annual review of biophysics and biomolecular structure.

[50]  A L Benabid,et al.  [Effects of the stimulation of the subthalamic nucleus in Parkinson disease]. , 1993, Revue neurologique.

[51]  J. Brotchie,et al.  Alleviation of parkinsonism by antagonism of excitatory amino acid transmission in the medial segment of the globus pallidus in rat and primate , 1991, Movement disorders : official journal of the Movement Disorder Society.

[52]  T. Aziz,et al.  Lesion of the subthalamic nucleus for the alleviation of 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP)‐induced parkinsonism in the primate , 1991, Movement disorders : official journal of the Movement Disorder Society.

[53]  B. Bloch,et al.  Dopamine receptor gene expression by enkephalin neurons in rat forebrain. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[54]  S. Fahn Adverse Effects of Levodopa in Parkinson’s Disease , 1989 .

[55]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .

[56]  F. James Rohlf,et al.  Biometry: The Principles and Practice of Statistics in Biological Research , 1969 .