Autoradiographic Analysis of [³H]Kainic Acid Binding in Primate Braind

References

• Shinozaki H., Konishi S. Actions of several antihelminthics and insecticides on rat cortical neurones. Brain Res. 1970; 24: 368–371
   PubMedGoogle Scholar
• Hall J. G., Hicks T. P., McLennan H. Kainic acid and the glutamate receptor. Neurosci. Lett. 1978; 8: 171–175
   Web of Science ®Google Scholar
• Watkins J. C., Evans R. M. Excitatory amino acid neurotransmitters. Ann. Rev. Pharmac. Toxicol. 1981; 21: 165–204
   PubMed Web of Science ®Google Scholar
• Coyle J. T., Schwarcz R. Lesion of striatal neurones with kainic acid provides a model for Huntington's disease. Nature 1976; 263: 244–246
   PubMed Web of Science ®Google Scholar
• Simon J. R., Contrera J. F., Kuhar M. J. Binding of 3H-kainic acid, an analogue of L-glutamate, to brain membranes. J. Neurochem. 1975; 26: 141–147
   Web of Science ®Google Scholar
• Coyle J. T., Molliver M. R., Kuhar M. J. In situ injection of kainic acid: a new method for selectively lesioning neuronal cell bodies while sparing axons of passage. J. Comp. Neurol. 1978; 180: 301–318
   PubMed Web of Science ®Google Scholar
• McGeer E. G., Olney J. W., McGeer P. L. Kainic acid as a Tool in Neurobiology. Raven Press, Publishers, New York 1978
   Google Scholar
• Coyle J. T., Schwarcz R. Lesion of striatal neurones with kainic acid provides a model for Huntington's disease. Nature 1976; 263: 244–246
   PubMed Web of Science ®Google Scholar
• McGeer E. G., McGeer P. L. Duplication of biochemical changes in Huntington's chorea by intrastriatal injections of glutamic and kainic acids. Nature 1976; 263: 517–519
   PubMed Web of Science ®Google Scholar
• Herndon R. M., Addicks E., Coyle J. T. Ultrastructural analysis of kainic acid lesion to cerebellar cortex. Neuroscience 1980; 5: 1015–1026
   PubMed Web of Science ®Google Scholar
• Zaczek R., Coyle J. T. Excitatory amino acid analogues; neurotoxicity and seizures. Neuropharmacology 1982; 21: 15–26
   PubMed Web of Science ®Google Scholar
• Biziere K., Coyle J. T. Influence of cortical striatal afferents on striatal kainic acid neurotoxicity. Neurosci. Lett. 1978; 8: 303–310
   PubMed Web of Science ®Google Scholar
• Kohler C., Schwarcz R., Fuxe K. Hippocampal lesions indicate differences between the excitotoxic properties of acidic amino acids. Brain Res. 1979; 175: 366–371
   PubMed Web of Science ®Google Scholar
• Ben-Ari Y. Limbic seizure and brain damage produced by kainic acid: mechanisms and relevance to human temporal lobe epilepsy. Neuroscience 1985; 14: 375–403
   PubMed Web of Science ®Google Scholar
• French E. D., Aldino C., Schwarcz R. Intrahippocampal kainic acid, seizures and local neuronal degeneration: relationships assessed in unanaesthetised rats. Neuroscience 1982; 7: 2525–2536
   PubMed Web of Science ®Google Scholar
• Margerison J. H., Corsellis J. A. N. Epilepsy and the temporal lobes. A clinical electroencephalographic and neuropathological study of the brain in epilepsy with particular reference to the temporal lobes. Brain 1965; 151: 457–467
   Google Scholar
• Ben-Ari Y., Tremblay E., Ottersen O. P., Naquet R. Evidence suggesting secondary epileptogenic lesions after kainic acid; pretreatment with diazepam reduces distant but not local brain damage. Brain Res. 1979; 165: 362–365
   PubMed Web of Science ®Google Scholar
• Berger B., Ben-Ari Y. Autoradiographic visualisation of [3H]-kainic acid receptor subtypes in the rat hippocampus. Neurosci. Lett. 1983; 39: 237–242
   PubMed Web of Science ®Google Scholar
• Hall H., Thor L. Evaluation of a semi-automated filtration technique for receptor binding studies. Life Sci. 1978; 24: 2293–2300
   Web of Science ®Google Scholar
• Slater P. A microcomputer-based image analyser for receptor autoradiography. Br. J. Pharmac. 1985; 85: 391P
   Google Scholar
• Geary W. A., Toga A. W., Wooten G. C. Quantitative film autoradiography for tritium: methodological considerations. Brain Res. 1985; 337: 99–108
   PubMed Web of Science ®Google Scholar
• Kuhar M. J., Unnerstall J. R. Quantitative receptor mapping by autoradiography: some current technical problems. Trends in Neurosci. 1985; 8: 49–53
   Web of Science ®Google Scholar
• Foster A. C., Mena E. E., Monaghan D. T., Cotman C. W. Synaptic localisation of kainic acid binding sites. Nature 1981; 289: 73–75
   PubMed Web of Science ®Google Scholar
• London E. D., Coyle J. T. Cooperative interactions at [3H]-kainic acid binding sites in rat and human cerebellum. Eur.J. Pharmac. 1979; 56: 287–291
   PubMed Web of Science ®Google Scholar
• Monaghan D. T., Cotman C. W. The distribution of [3H]-kainic acid binding sites in rat CNS as determined by autoradiography. Brain Res. 1982; 252: 91–100
   PubMed Web of Science ®Google Scholar
• Unnerstall J. R., Wamsley J. K. Autoradiographic localisation of high-affinity [3H]-kainic acid binding sites in the rat forebrain. Eur. J. Pharmac. 1983; 86: 361–371
   PubMed Web of Science ®Google Scholar
• Tremblay E., Represa A., Ben-Ari Y. Autoradiographic localisation of kainic acid binding sites in the human hippocampus. Brain Res. 1985; 343: 378–382
   PubMed Web of Science ®Google Scholar
• Geddes J. W., Monaghan D. T., Cotman C. W., Lott I. T., Kim R. C., Chui M. C. Plasticity of hippocampal circuitry in Alzheimers disease. Science 1985; 230: 1179–1181
   PubMed Web of Science ®Google Scholar
• Schwarcz R., Fuxe K. 3H-Kainic acid binding: relevance for evaluating the neurotoxicity of kainic acid. Life Sci. 1979; 24: 1471–1480
   PubMed Web of Science ®Google Scholar
• Nadi N. S., McBride W. J., Rhode B. Distribution of several amino acids in regions of the cerebellum in the rat. J. Neurochem. 1977; 28: 453–455
   PubMed Web of Science ®Google Scholar
• Rea M. A., McBride W. J., Rhode B. Regional and synaptosomal levels of amino acid neurotransmitters in the 3-acetylpyridine deafferented rat cerebellum. J. Neurochem. 1980; 34: 1106–1108
   PubMed Web of Science ®Google Scholar
• Greenamyre J. T., Olsen J. M. M., Penney J. B., Young A. B. Autoradiographic characterisation of N-methyl-D-aspartate-, quisqualate-, and kainate-sensitive glutamate binding sites. J. Pharmac. exp. Ther. 1985; 233: 254–263
   PubMed Web of Science ®Google Scholar
• Lund-Karlson R., Fonnum F. Evidence for glutamate as a neurotransmitter in the corticofugal fibres to the lateral geniculate body and the superior colliculus in rats. Brain Res. 1978; 151: 457–467
   PubMed Web of Science ®Google Scholar
• Monaghan D. T., Yao D., Olverman H. J., Watkins J. C., Cotman C. W. Autoradiography of [3H]-amino-5-phosphonopentanoate binding sites in rat brain. Neurosci. Lett. 1984; 52: 253–258
   PubMed Web of Science ®Google Scholar
• French J. B., Gernandt B. E., Livingstone R. B. Regional differences in seizure susceptibility in monkey cortex. Arch. Neurol. Psychiat. 1956; 75: 260–274
   Google Scholar