The AMPA receptors of auditory neurons

Hearing Research

Volumn 147, Issue 1-2, 2000, Pages 77-91

  Parks, Thomas N ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Calcium permeable; Cochlear nucleus; Glutamate receptor; Nucleus magnocellularis; Rapid desensitization

Indexed keywords

6 CYANO 7 NITRO 2,3 QUINOXALINEDIONE; 6 NITRO 7 SULFAMOYLBENZO[F]QUINOXALINE 2,3 DIONE; 6,7 DINITRO 2,3 QUINOXALINEDIONE; AMPA RECEPTOR; GLUTAMATE RECEPTOR;

AUDITORY NERVOUS SYSTEM; BRAIN STEM; CALCIUM TRANSPORT; CENTRAL NERVOUS SYSTEM; COCHLEAR NUCLEUS; MAGNOCELLULAR NUCLEUS; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; REVIEW;

EID: 0033846659     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(00)00122-2     Document Type: Article

References (92)

1. Angulo M.C., Lambolez B., Audinat E., Hestrin S., Rossier J. Subunit composition, kinetic, and permeation properties of AMPA receptors in single neocortical nonpyramidal cells. J. Neurosci. 17:1997;6685-6696.
2. Banks M.I., Smith P.H. Intracellular recording from neurobiotin-labeled cells in brain slices of the rat medial nucleus of the trapezoid body. J. Neurosci. 12:1992;2819.
3. Barnes-Davies M., Forsythe I.D. the binaural auditory pathway: excitatory amino acid receptors mediate dual timecourse excitatory postsynaptic currents in the rat medial nucleus of the trapezoid body. Proc. R. Soc. Lond. B Biol. Sci. 251:1993;151-157.
4. Barnes-Davies M., Forsythe I.D. Pre- and postsynaptic glutamate receptors at a giant excitatory synapse in rat auditory brainstem slices. J. Physiol. 488:1995;387-406.
5. Borges K., Dingledine R. AMPA receptors: Molecular and functional diversity. Prog. Brain Res. 116:1998;153-170.
6. Caicedo A., Eybalin M. Glutamate receptor phenotypes in the auditory brainstem and mid-brain of the developing rat. Eur. J. Neurosci. 11:1999;51-74.
7. 2+ permeability of glutamate receptors. Eur. J. Neurosci. 10:1998;941-954.
8. Caspary D.M., Faingold C.L. Non-N-methyl-D-aspartate receptors may mediate ipsilateral excitation at lateral superior olivary synapses. Brain Res. 503:1989;83-90.
9. Chittajallu R., Braithwaite S.P., Clarke V.R., Henley J.M. Kainate receptors: subunits, synaptic localisation, and function. Trends Pharmacol. Sci. 20:1999;26-35.
10. Collingridge G.L., Lester R.A.J. Excitatory amino acid receptors in the vertebrate central nervous system. Pharmacol. Rev. 40:1989;144-209.
11. Danysz W., Lanthorn T. Uncompetitive NMDA receptor antagonists-is low-affinity better? Amino Acids. 17:1999;10-11.
12. Dingledine R., Borges K., Bowie D., Traynelis S.F. The glutamate receptor ion channels. Pharmacol. Rev. 51:1999;7-61.
13. Feldman D.E., Knudsen E.I. NMDA and non-NMDA glutamate receptors in auditory transmission in the barn owl inferior colliculus. J. Neurosci. 14:1994;5939-5958.
14. Ferragamo M.J., Golding N.L., Oertel D. Synaptic inputs to stellate cells in the ventral cochlear nucleus. J. Neurophysiol. 79:1998;51-63.
15. Gallo V., Upson J.M., Hayes W.P., Vyklicky L.J., Winters C.A., Buonanno A. Molecular cloning and developmental analysis of a new glutamate receptor subunit isoform in cerebellum. J. Neurosci. 12:1992;1010-1023.
16. Gardner S.M., Trussell L.O., Oertel D. Time course and permeation of synaptic AMPA receptors in cochlear nuclear neurons correlate with input. J. Neurosci. 19:1999;8721-8729.
17. Gaza W.C., Ribak C.E. Immunocytochemical localization of AMPA receptors in the rat inferior colliculus. Brain Res. 774:1997;175-183.
18. 2+ permeability of AMPA receptors in principal and interneurons in rat CNS. Neuron. 15:1995;193-204.
19. Hack N.J., Wride M.C., Charters K.M., Kater S.B., Parks T.N. Developmental changes in the subcellular localization of calretinin. J. Neurosci. 20:2000;RC67.
20. Hackett J.T., Jackson H., Rubel E.W. Synaptic excitation of the second and third order auditory neurons in the avian brain stem. Neuroscience. 7:1982;1455-1469.
21. Hollmann M., Heinemann S. Cloned glutamate receptors. Ann. Rev. Neurosci. 17:1994;31-108.
22. Hunter C., Petralia R.S., Vu T., Wenthold R.J. Expression of AMPA-selective glutamate receptor subunits in morphologically defined neurons of the mammalian cochlear nucleus. J. Neurosci. 13:1993;1932-1946.
23. Isaacson J.S., Walmsley B. Receptors underlying excitatory synaptic transmission in slices of the rat anteroventral cochlear nucleus. J. Neurophysiol. 73:1995;964-973.
24. Jackson H., Nemeth E.F., Parks T.N. Non-N-methyl-D-aspartate receptors mediating synaptic transmission in the avian cochlear nucleus: Effects of kynurenic acid, dipicolinic acid and streptomycin. Neuroscience. 16:1985;171-179.
25. Kandler K., Friauf E. Development of glycinergic and glutamatergic synaptic transmission in the auditory brainstem of perinatal rats. J. Neurosci. 15:1995;6890-6904.
26. Kidd F.L., Isaac J.T.R. Developmental and activity-dependent regulation of kainate receptors at thalamocortical synapses. Nature. 400:1999;569-573.
27. Kubke M.F., Carr C.E. Development of AMPA-selective glutamate receptors in the auditory brainstem of birds. Microsc. Res. Tech. 41:1998;176-186.
28. Kubke, M.F. and Carr, C.E., 2000. Development of the auditory brainstem of birds: Comparison between barn owls and chickens. Hear. Res., in press.
29. Kuriyama H., Jenkins O., Altschuler R.A. Immunocytochemical localization of AMPA selective glutamate receptor subunits in the rat cochlea. Hear. Res. 80:1994;233-240.
30. Lawrence J.J., Trussell L.O. Developmental regulation of AMPA receptor kinetics in the avian cochlear nucleus. Soc. Neurosci. Abstr. 24:1998;846.
31. Lee J.C., Greig A., Ravindranathan A., Parks T.N., Rao M.S. Molecular analysis of AMPA-specific receptors: subunit composition, editing, and calcium influx determination in small amounts of tissue. Brain Res. Protoc. 3:1998;142-154.
32. Levin M.D., Kubke M.F., Schneider M., Wenthold R., Carr C.E. Localization of AMPA-selective glutamate receptors in the auditory brain stem of the barn owl. J. Comp. Neurol. 378:1997;239-253.
33. Lodge, D. (1997) Subtypes of glutamate receptors: Historical perspectives on their pharmacological differentiation. In: Monaghan, D.T. and Wenthold, R.J. (Eds.), The Ionotropic Glutamate Receptors. Humana Press, Totowa, NJ, pp. 1-38.
34. Lomeli H., Mosbacher J., Melcher T., Hoger T., Geiger J.R.P., Monyer H., Higuchi M., Bach A., Seeburg P.H. Control of kinetic properties of AMPA receptors by nuclear RNA editing. Science. 266:1994;1709-1713.
35. Luo L., Brumm D., Ryan A.F. Distribution of non-NMDA glutamate receptor mRNAs in the developing rat cochlea. J. Comp. Neurol. 361:1995;372-382.
36. Manis P.B., Molitor S.C. N-methyl-D-aspartate receptors at parallel fiber synapses in the dorsal cochlear nucleus. J. Neurophysiol. 76:1996;1639-1656.
37. Martin M.R. Excitatory amino acid pharmacology of the auditory nerve and nucleus magnocellularis of the chicken. Hear. Res. 17:1985;153-160.
38. Matsubara A., Laske J.H., Davanger S., Usami S., Ottersen O.P. Organization of AMPA receptor subunits at a glutamate synapse: a quantitative immunogold analysis of hair cell synapses in the rat organ of Corti. J. Neurosci. 16:1996;4457-4467.
39. Meldrum B. The glutamate synapse as a therapeutic target: Perspectives for the future. Prog. Brain Res. 116:1998;441-458.
40. Michaelis E.K. Molecular biology of glutamate receptors in the central nervous system and their role in excitotoxicity, oxidative stress and aging. Prog. Neurobiol. 54:1998;369-415.
41. Moore D.R., Kotak V.C., Sanes D.H. Commissural and lemniscal synaptic input to the gerbil inferior colliculus. J. Neurophysiol. 80:1998;2229-2236.
42. Mosbacher J., Schoepfer R., Monyer H., Burnashev N., Seeburg P.H., Ruppersberg J.P. A molecular determinant for submillisecond desensitization in glutamate receptors. Science. 266:1994;1059-1061.
43. Myers S.J., Dingledine R., Borges K. Genetic regulation of glutamate receptor ion channels. Ann. Rev. Pharmcol. Toxicol. 39:1999;221-241.
44. Nakagawa T., Komune S., Uemura T., Akaike N. Excitatory amino acid response in isolated spiral ganglion cells of guinea pig cochlea. J. Neurophysiol. 65:1991;715-723.
45. Nemeth E.F., Jackson H., Parks T.N. Pharmacological evidence for synaptic transmission mediated by non-N-methyl-D-aspartate receptors in the avian cochlear nucleus. Neurosci. Lett. 40:1983;39-44.
46. Niedzielski A.S., Wenthold R.J. Expression of AMPA, kainate, and NMDA receptor subunits in cochlear and vestibular ganglia. J. Neurosci. 15:1995;2338-2353.
47. Niedzielski A.S., Saffieddine S., Wenthold R.J. Molecular analysis of excitatory amino acid receptor expression in the cochlea. Audiol. Neurootol. 2:1997;79-91.
48. 2+ permeability mediate synaptic transmission in the avian auditory pathway. J. Physiol. 482:1995;309-315.
49. Paternain A.V., Morales M., Lerma J. Selective antagonism of AMPA receptors unmasks kainate-receptor mediated responses in hippocampal neurons. Neuron. 14:1995;185-189.
50. Petralia, R.S. (1997) Immunocytochemical localization of ionotropic glutamate receptors (GluRs) in neural circuits. In: Monaghan, D.T. and Wenthold, R.J. (Eds.), The Ionotropic Glutamate Receptors. Humana Press, Totowa, NJ, pp. 219-263.
51. Petralia R.S., Wang Y.-X., Zhao H.-M., Wenthold R.J. Ionotropic and metabotropic glutamate receptors show unique postsynaptic, presynaptic, and glial localizations in the dorsal cochlear nucleus. J. Comp. Neurol. 372:1996;356-383.
52. Petralia R.S., Wang Y.-X., Mayat E., Wenthold R.J. Glutamate receptor subunit 2-selective antibody shows a differential distribution of calcium-impermeable AMPA receptors among populations of neurons. J. Comp. Neurol. 385:1997;456-476.
53. Petralia R.S., Wenthold R.J. Light and electron immunocytochemical localization of AMPA-selective glutamate receptors in the rat brain. J. Comp. Neurol. 318:1992;329-354.
54. Pruss R.M., Akeson R.L., Racke M.M., Wilburn J.L. Agonist-activated cobalt uptake identifies divalent cation-permeable kainate receptors on neurons and glial cells. Neuron. 7:1991;509-518.
55. Puel J.L. Chemical synaptic transmission in the cochlea. Prog. Neurobiol. 47:1995;449-476.
56. Raman I., Zhang S., Trussell L.O. Pathway-specific variants of AMPA receptors and their contributions to neuronal signaling. J. Neurosci. 14:1994;4998-5010.
57. Ravindranathan A., Parks T.N., Rao M.S. New isoforms of the chick glutamate receptor subunit GluR4: molecular cloning, regional expression and developmental analysis. Brain Res. Mol. Brain Res. 50:1997;143-153.
58. Ravindranathan A., Donevan S.D., Sugden S., Greig A., Rao M.S., Parks T.N. Contrasting molecular compositions and channel properties of AMPA receptors on chick auditory and brainstem motor neurons. J. Physiol. 523:(3):2000;667-684.
59. Reng D., Hack I., Muller M., Smolders J.W.T. AMPA-type glutamate receptor subunits are expressed in the avian cochlear hair cells and ganglion cells. NeuroReport. 10:1999;2137-2141.
60. Rogers S.W., Hughes T.E., Hollmann M., Gasic G.P., Deneris E.S., Heinemann S. The characterization and localization of the glutamate receptor subunit GluR1 in the rat brain. J. Neurosci. 11:1991;2713-2724.
61. Rubel, E.W. and Parks, T.N., 1988. Organization and development of the avian brainstem auditory system. In: Edelman, G.M., Gall, W.E. and Cowan, W.M. (Eds.), Auditory Function: Neurobiological Bases of Hearing. New York, Wiley-Interscience, pp. 3-92.
62. Rubio M.E., Wenthold R.J. Glutamate receptors are selectively targeted to postsynaptic sites in neurons. Neuron. 18:1997;939-950.
63. Ruel J., Chen C., Bobbin R.P., Puel J.L. AMPA-preferring glutamate receptors in cochlear physiology of adult guinea-pig. J. Physiol. (Lond.). 518:1999;667-680.
64. Ryan A.F., Brumm D., Kraft M. Occurrence and distribution of non-NMDA glutamate receptor mRNAs in the cochlea. NeuroReport. 2:1991;643-646.
65. Safieddine S., Eybalin M. Co-expression of NMDA and AMPA/kainate receptor mRNAs in cochlear neurones. NeuroReport. 3:1991;1145-1148.
66. Sato K., Kiyama H., Tohyama M. The differential expression patterns of messenger RNAs encoding non-N-methyl-D-aspartate glutamate receptor subunits (GluR1-4) in the rat brain. Neuroscience. 52:1993;515-539.
67. Sewell, W.F., 1997. Biochemistry and pharmacology of the auditory system. In: Crocker, M.J. (Ed.), Encyclopedia of Acoustics. J. Wiley and Sons, New York, pp. 1401-1408.
68. Simmons D.D., Song C., Giboney P. Kainic acid stimulates uptake of divalent cations in postnatal cochlear neurons. NeuroReport. 5:1994;1433-1437.
69. Sugden, S., Ravindranathan, A., Rao, M.S. and Parks, T.N., 1999. Developmental changes in the structure of AMPA receptors in the chick brainstem auditory system. Abstracts of the Midwinter Meeting of the Association for Research in Otolaryngology, p. 68.
70. Swanson G.T., Kamboj S.K., Cull-Candy S.G. Single-channel properties of recombinant AMPA receptors depend on RNA editing, splice variation, and subunit composition. J. Neurosci. 17:1997;58-69.
71. Trussell L.O. Cellular mechanisms for preservation of timing in central auditory pathways. Curr. Opin. Neurobiol. 7:1997;487-492.
72. Trussell L. Control of time course of glutamatergic synaptic currents. Prog. Brain Res. 116:1998;59-69.
73. Trussell L.O. Synaptic mechanisms for coding timing in auditory neurons. Ann. Rev. Physiol. 61:1999;477-496.
74. Vitten H., Friauf E., Peichl L., Lohrke S. Kainate receptor mediated currents in lateral superior olive neurons of the rat. Soc. Neursci. Abstr. 25:1999;974.
75. Wagner T. Lemniscal input to identified neurons of the central nucleus of mouse inferior colliculus: an intracellular brain slice study. Eur. J. Neurosci. 8:1996;1231-1239.
76. Waller H.J., Godfrey D.A., Chen K. Effects of parallel fiber stimulation on neurons of rat dorsal cochlear nucleus. Hear. Res. 98:1996;169-179.
77. Walmsley B., Alvarez F.J., Fyffe R.E. Diversity of structure and function at mammalian central synapses. Trends Neurosci. 21:1998;81-88.
78. Watkins J.C., Krogsgaard-Larsen P., Honore T. Structure-activity relationships in the development of excitatory amino acid receptor agonists and competitive antagonists. Trends Pharmacol. Sci. 11:1990;25-33.
79. Webber T.J., Green E.J., Winters R.W., Schneiderman N., McCabe P.M. Contribution of NMDA and non-NMDA receptors to synaptic transmission from the brachium of the inferior colliculus to the medial subdivision of the medial geniculate nucleus in the rabbit. Exp. Brain Res. 124:1999;295-303.
80. Wang Y.X., Wenthold R.J., Ottersen O.P., Petralia R.S. Endbulb synapses in the anteroventral cochlear nucleus express a specific subset of AMPA-type glutamate receptor subunits. J. Neurosci. 18:1998;1148-1160.
81. Washburn M.S., Numberger M., Zhang S., Dingledine R. Differential dependence on GluR2 expression of three characteristic features of AMPA receptors. J. Neurosci. 17:1997;9393-9406.
82. Wenthold R.J., Roche K.W. The organization and regulation of non-NMDA receptors in neurons. Prog. Brain Res. 116:1998;133-152.
83. Wenthold R.J., Yokotani N., Doi K., Wada K. Immunochemical characterization of the non-NMDA glutamate receptor using subunit-specific antibodies. J. Biol. Chem. 267:1992;501-507.
84. Wu S.H., Fu X.W. Glutamate receptors underlying excitatory synaptic transmission in the rat's lateral superior olive studied in vitro. Hear. Res. 122:1998;47-59.
85. Wu S.H., Kelly J.B. Synaptic pharmacology of the superior olivary complex sudied in mouse brain slice. J. Neurosci. 12:1992;3084-3097.
86. Wu S.H., Kelly J.B. In vitro brain slice studies of the rat's dorsal nucleus of the lateral lemniscus. III. synaptic pharmacology. J. Neurophysiol. 75:1996;1271-1282.
87. Zhou N., Parks T.N. Pharmacology of excitatory amino acid neurotransmission in nucleus laminaris of the chick. Hear. Res. 52:1991;195-200.
88. Zhou N., Parks T.N. Developmental changes in the effects of drugs acting at NMDA or non-NMDA receptors on synaptic transmission in the chick cochlear nucleus (nuc. magnocellularis). Dev. Brain Res. 67:1992;145-152.
89. Zhou N., Parks T.N. γ-D-glutamylaminomethyl sulfonic acid (GAMS) distinguishes subtypes of glutamate receptor in the chick cochlear nucleus (nuc. magnocellularis). Hear. Res. 60:1992;20-26.
90. Zhou N., Parks T.N. Maintenance of pharmacologically-immature glutamate receptors by aberrant synapses in the chick cochlear nucleus. Brain Res. 628:1993;149-156.
91. Zhou N., Hammerland L.G., Parks T.N. γ-D-glutamylaminomethyl sulfonic acid (GAMS) distinguishes kainic acid- from AMPA-induced responses in Xenopus oocytes expressing chick brain glutamate receptors. Neuropharmacology. 32:1993;767-775.
92. Zhou N., Taylor D.A., Parks T.N. Cobalt-permeable non-NMDA receptors in developing chick brain stem auditory nuclei. NeuroReport. 6:1995;2273-2276.