L-Glutamate Receptor Heterogeneity: Labeling of Distinct Receptor Sub-Types Using Radioligand Binding Techniques

References

• Watkins J. C., Evans R. H. Excitatory Amino Acid Transmitters. Ann. Rev. Pharmacol. Toxicol. 1981; 21: 165–204
   PubMed Web of Science ®Google Scholar
• Fagg G. E., Foster A. C. Amino Acid Neurotransmitters and Their Pathways in the Mammalian Central Nervous System. Neuroscience 1983; 9: 701–719
   PubMed Web of Science ®Google Scholar
• Foster A. C., Fagg G. E. Acidic Amino Acid Binding Sites in Mammalian Neuronal Membranes: their Characteristics and Relationship to Synaptic Receptors. Brain Res. Rev. 1984, in press
   Google Scholar
• Snyder S. H., Bennett J. P. Neurotransmitter Receptors in the Brain: Biochemical Identification. Ann Rev. Physiol. 1976; 38: 153–175
   PubMed Web of Science ®Google Scholar
• Fagg G. E., Foster A. C., Mena E. E., Cotman C. W. Chloride and Calcium Ions Reveal a Pharmacologically Distinct Population of L-Glutamate Binding Sites in Synaptic Membranes: Correspondence between Biochemical and Electrophysiological Data. J. Neurosci. 1982; 2: 958–965
   PubMed Web of Science ®Google Scholar
• Fagg G. E., Foster A. C., Mena E. E., Cotman C. W. Chloride and Calcium Ions Separate L-Glutamate Receptor Populations in Synaptic Membranes. Europ. J. Pharmacol. 1983; 88: 105–110
   PubMedGoogle Scholar
• Fagg G. E., Mena E. E., Cotman C. W. L-Glutamate Receptor Populations in Synaptic Membranes: Effects of Ions and Pharmacological Characteristics. Adv. Biochem. Psychopharmacol. 1983; 37: 199–209
   PubMedGoogle Scholar
• Fagg G. E., Mena E. E., Monaghan D. T., Cotman C. W. Freezing Eliminates a Specific Population of L-Glutamate Receptors in Synaptic Membranes. Neurosci. Lett. 1983; 38: 157–162
   PubMed Web of Science ®Google Scholar
• Jones D. H., Matus A. I. Isolation of Synaptic Plasma Membranes from Brain by Combined Flotation-Sedimentation Density Gradient Centrifugation. Biochim. Biophys. Acta. 1974; 356: 276–287
   PubMed Web of Science ®Google Scholar
• Cotman C. W., Kelly P. T. Macromolecular Architecture of CNS Synpases. The Cell Surface and Neuronal Function, C. W. Cotman, G. Poste, G.L. Nicolson. Elsevier, Amsterdam 1980; 505–533
   Google Scholar
• Gray E. G. Electron Microscopy of Excitatory and Inhibitory Synapses: a Brief Review. Prog. Brain Res. 1969; 31: 141–155
   PubMedGoogle Scholar
• Matus A. I., Taff-Jones D. H. Morphology and Molecular Composition of Isolated Postsynaptic Junctional Structures. Proc. R. Soc. Lond. B. 1978; 203: 135–151
   PubMedGoogle Scholar
• Cohen R. S., Blomberg F., Berzins K., Siekevitz P. The Structure of Postsynaptic Densities Isolated from Dog Cerebral Cortex. J. Cell Biol. 1977; 74: 181–203
   PubMed Web of Science ®Google Scholar
• Matus A. I., Pehling G., Wilkinson D. γ-Amino-butyric Acid Receptors in Brain Postsynaptic Densities. J. Neurobiol. 1981; 12: 67–73
   PubMedGoogle Scholar
• Evans R. H., Francis A. A., Hunt K., Oakes D. J., Watkins J. C. The Effect of a Series of ω-Phosphonic-α-Carboxylic Amino Acids on Electrically-Evoked and Excitant Amino Acid-Induced Responses in Isolated Spinal Cord Preparations. Br. J. Pharmacol. 1982; 75: 65–75
   PubMed Web of Science ®Google Scholar
• Honoré T., Lauridsen J., Krogsgaard-Larsen P. The Binding of [3H]AMPA, a Structural Analogue of Glutamic Acid, to Rat Brain Membranes. J. Neurochem. 1982; 38: 173–178
   PubMed Web of Science ®Google Scholar
• Harris E. W., Cotman C. W. Effects of Acidic Amino Acid Anatagonists on Paired-Pulse Potentiation at the Lateral Perforant Path. Exp. Brain Res. 1983; 52: 455–460
   PubMedGoogle Scholar
• Ferkany J. W., Zaczek R., Coyle J. T. Kainic Acid Stimulates Excitatory Amino Acid Neurotransmitter Release at Presynaptic Receptors. Nature (Lond.) 1982; 298: 757–759
   PubMedGoogle Scholar
• Collins G. G.S., Anson J., Surtees L. Presynaptic Kainate and N-Methyl-D-Aspartate Receptors Regulate Excitatory Amino Acid Release in the Olfactory Cortex. Brain Res. 1983; 265: 157–159
   PubMedGoogle Scholar
• Foster A. C., Mena E. E., Monaghan D. T., Cotman C. W. Synaptic Localization of Kainic Acid Binding Sites. Nature (Lond.) 1981; 289: 73–75
   PubMed Web of Science ®Google Scholar
• Dilber A., Henke H., Cuénod M., Winterhalter K. Characterization of the Low Affinity Kainic Acid Binding Site Solubilized from Pigeon Cerebellum. Abstr. Soc. Neurosci. 1983; 9: 260
   Google Scholar
• Foster A. C., Roberts P. J. High-Affinity L-[3H]-Glutamate Binding to Postsynaptic Sites on Rat Cerebellar Membranes. J. Neurochem. 1978; 31: 1467–1477
   PubMedGoogle Scholar
• Baudry M., Lynch G. Characterization of Two [3H]Glutamate Binding Sites in Rat Hippocampal Membranes. J. Neurochem. 1981; 36: 811–820
   PubMedGoogle Scholar
• DiLauro A., Meek J. L., Costa E. Specific High Affinity Binding of L-[3H]Aspartate to Rat Brain Membranes. J. Neurochem. 1982; 38: 1261–1267
   PubMedGoogle Scholar
• Napias C., Bergman M. O., Van Ness P. C., Greenlee D. V., Olsen R. W. GABA Binding in Mammalian Brain: Inhibition by Endogenous GABA. Life Sci. 1980; 27: 1001–1011
   PubMed Web of Science ®Google Scholar
• Gardner C. R., Klein J., Grove J. Endogenous GABA Determines the Characteristics of [3H]GABA Binding. Europ. J. Pharmacol. 1981; 75: 83–92
   PubMedGoogle Scholar