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Excitatory amino acidergic pathways and receptors in the basal ganglia

dc.contributor.authorDure, Leon S. IVen_US
dc.contributor.authorYoung, Anne B.en_US
dc.contributor.authorHollingsworth, Zane R.en_US
dc.contributor.authorPenney, John B.en_US
dc.contributor.authorMakowiec, Richard L.en_US
dc.contributor.authorSakurai, Sharin Y.en_US
dc.contributor.authorAlbin, Roger L.en_US
dc.date.accessioned2006-09-08T19:34:44Z
dc.date.available2006-09-08T19:34:44Z
dc.date.issued1991-10en_US
dc.identifier.citationAlbin, R. L.; Makowiec, R. L.; Hollingsworth, Z.; Sakurai, S. Y.; Dure, L. S.; Penney, J. B.; Young, A. B.; (1991). "Excitatory amino acidergic pathways and receptors in the basal ganglia." Amino Acids 1(3): 339-350. <http://hdl.handle.net/2027.42/41734>en_US
dc.identifier.issn1438-2199en_US
dc.identifier.issn0939-4451en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41734
dc.description.abstractThe striatum receives the majority of excitatory amino acidergic input to the basal ganglia from neocortical and allocortical sources. The subthalamic nucleus and the substantia nigra also receive excitatory amino acidergic inputs from neocortex. The subthalamic nucleus, which has prominent projections to the pallidum and nigra, is the only known intrinsic excitatory amino acidergic component of the basal ganglia. Possible excitatory amino acidergic inputs reach the basal ganglia from the intralaminar thalamic nuclei and the pedunculo-pontine nucleus. The striatum is richly endowed with all subtypes of excitatory amino acid receptors and these appear to be inhomogeneously distributed within the striatal complex. The non-striatal nuclei contain lesser levels of excitatory amino acid receptors and the relative proportion of these receptors varies between nuclei. The presence of high densities of excitatory amino acid receptors is a phylogenetically conserved feature of the striatum and its non-mammalian homologues. In Huntington's disease, there is substantial depletion of α -amino-3-hydroxy-5-methylisoxazole-4-propionic acid, N-methyl-D-aspartate, and kainate receptors within the striatum. In Parkinson's disease substantia nigra, there is significant loss of N-methyl-D-aspartate and α -amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors.en_US
dc.format.extent1884526 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherSubthalamic Nucleusen_US
dc.subject.otherBiochemical Engineeringen_US
dc.subject.otherProteomicsen_US
dc.subject.otherLife Sciencesen_US
dc.subject.otherLife Sciences, Generalen_US
dc.subject.otherPallidumen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherAnalytical Chemistryen_US
dc.subject.otherNeurobiologyen_US
dc.subject.otherGlutamateen_US
dc.subject.otherAmino Acidsen_US
dc.subject.otherα -Amino-3-Hydroxy-5-Methylisoxazole-4-Propionic Aciden_US
dc.subject.otherN-Methyl-D-asparateen_US
dc.subject.otherKainateen_US
dc.subject.otherStriatumen_US
dc.subject.otherAspartateen_US
dc.subject.otherSubstantia Nigraen_US
dc.titleExcitatory amino acidergic pathways and receptors in the basal gangliaen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USA; Department of Neuroscience Program, University of Michigan, Neuroscience Laboratory Building, 1103 E. Huron, 48104-1687, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USA; Department of Neuroscience Program, University of Michigan, Neuroscience Laboratory Building, 1103 E. Huron, 48104-1687, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neuroscience Program, University of Michigan, Neuroscience Laboratory Building, 1103 E. Huron, 48104-1687, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumDepartment of Neurology, University of Michigan, Ann Arbor, MI, USA; Department of Neuroscience Program, University of Michigan, Neuroscience Laboratory Building, 1103 E. Huron, 48104-1687, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid24194174en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41734/1/726_2004_Article_BF00814003.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00814003en_US
dc.identifier.sourceAmino Acidsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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