Expression of glycine receptor subunit mRNAs in the rat cochlear nucleus

Hearing Research

Volumn 144, Issue 1-2, 2000, Pages 47-52

  Sato, Kazuo ^a,b   Kuriyama, Hiromichi ^a,b   Altschuler, Richard A ^a  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^b KANSAI MEDICAL UNIVERSITY   (Japan)

Author keywords

Auditory; Brainstem; Glycine; In situ hybridization

Indexed keywords

GLYCINE RECEPTOR; MESSENGER RNA; RECEPTOR SUBUNIT; SULFUR 35;

ANIMAL TISSUE; ARTICLE; CELL SHAPE; CELL TYPE; COCHLEAR NUCLEUS; CONTROLLED STUDY; GENE EXPRESSION; GRANULE CELL; IN SITU HYBRIDIZATION; MALE; NONHUMAN; PERIKARYON; PRIORITY JOURNAL; RAT; SILVER STAINING; TISSUE DISTRIBUTION;

ANIMALS; COCHLEAR NUCLEUS; IN SITU HYBRIDIZATION; MALE; PROTEIN ISOFORMS; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, GLYCINE; RNA, MESSENGER;

EID: 0034073785     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(00)00044-7     Document Type: Article

References (54)

1. Adams, J.C., 1993. Non-primary inputs to the cochlear nucleus visualized using immunocytochemistry. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A. Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 133-141.
2. Altschuler R.A., Betz H., Parakkal M.H., Reeks K.A., Wenthold R.J. Identification of glycinergic synapses in the cochlear nucleus through immunocytochemical localization of the postsynaptic receptor. Brain Res. 369:1986;316-320.
3. Altschuler, R.A., Juiz, J.M., Shore, S.E., Bledsoe, S.C., Helfert, R.H., Wenthold, R.J., 1993. Inhibitory amino acid synapses and pathway in the ventral cochlear nucleus. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A., Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 211-224.
4. Backoff P.M., Palombi P.S., Caspary D.M. Glycinergic and GABAergic inputs affect short-term suppression in the cochlear nucleus. Hear. Res. 110:1997;155-163.
5. Betz H., Becker C.-M. The mammalian glycine receptor: biology and structure of a neuronal chloride channel protein. Neurochem. Int. 13:1988;137-146.
6. Betz H., Langosch D., Hoch W., Prior P., Pribilla I., Kuhse J., Schmieden V., Malosio M.-L., Matzenbach B., Holzinger F. Structure and expression of inhibitory glycine receptors. Adv. Exp. Med. Biol. 287:1991;421-429.
7. Betz H., Kuhse J., Schmieden V., Laube B., Kirsch J., Harvery R.J. Structure and function of inhibitory and excitatory glycine receptors. Ann. New York Acad. Sci. 868:1999;667-676.
8. Cant, N.B., Morest, D.K., 1984. The structural basis for stimulus coding in the cochlear nucleus of the cat. In: Berlin, C. (Ed.), Hearing Science. College Hill Press, San Diego, CA, pp. 371-422.
9. Caspary, D.M., 1986. Cochlear nuclei: functional neuropharmacology of the principal cell types. In: Altschuler, R.A., Hoffmann, D.W., Bobbin, R.P. (Eds.), Neurobiology of Hearing: The Cochlea. Raven Press, New York, NY, pp. 303-332.
10. Caspary D.M., Havey D.C., Faingold C.L. Effects of microiontophoretically applied GLY and GABA on neuronal response patterns in the cochlear nuclei. Brain Res. 172:1979;179-185.
11. Caspary, D.M., Rybak, L.P., Faingold, C.L., 1985. The effects of excitatory and inhibitory amino acid neurotransmitters on the response properties of brainstem auditory neurons. In: Drescher, D.G. (Ed.), Auditory Biochemistry. Thomas, Springfield, IL, pp. 198-226.
12. Caspary, D.M., Palombi, P.S., Backoff, P.M., Helfert, R.H., Finlayson, P.G., 1993. GABA and glycine inputs control discharge rate within the excitatory response area of primary-like and phase-locked AVCN neurons. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A., Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 239-252.
13. Ehrlich I., Ilic V., Lohmann C., Friauf E. Development of glycinergic transmission in organotypic cultures from auditory brain stem. Neuroreport. 9:1998;2785-2790.
14. Evans, E.F., Zhao, W., 1993. Neuropharmacological and neurophysiological dissection of inhibition in the mammalian dorsal cochlear nucleus. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A., Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 253-266.
15. Friauf E., Hammerschmidt B., Kirsch J. Development of adult-type inhibitory glycine receptors in the central auditory system of rats. J. Comp. Neurol. 385:1997;117-134.
16. 3H ] strychnine binding sites. Brain Res. Bull. 15:1985;473-486.
17. Fubara B.M., Cassesay J.H., Covery E., Schwartz-Bloom R.D. Distribution of GABAA, GABAB and glycine receptors in the central auditory system of the big brown bat. J. Comp. Neurol. 369:1996;83-92.
18. Fujita M., Sato M., Inoue T., Kozuka T., Tohyama M. Regional distribution of the cells expressing glycine receptor β subunit mRNA in the rat brain. Brain Res. 560:1991;23-37.
19. Glendenning K.K., Baker B.N. Neuroanatomical distribution of receptors for three potential inhibitory neurotransmitters in the brainstem auditory nuclei of the cat. J. Comp. Neurol. 275:1988;288-308.
20. Godfrey, D.A., Parli, J.A., Dunn, J.D., Ross, C.D., 1988. Neurotransmitter microchemistry of the cochlear nucleus and the superior olivary complex. In: Syka, J., Masterton, R.L. (Eds.), Auditory Pathways. Plenum Press, New York, NY, pp. 107-121.
21. Golding N.L., Oertel D. Context dependent synaptic action of glycinergic and GABAergic inputs in the dorsal cochlear nucleus. J. Neurosci. 16:1996;2208-2219.
22. Harty T.P., Manis P.B. Glycine-evoked currents in acutely dissociated neurons of the guinea pig ventral cochlear nucleus. J. Neurophysiol. 75:1996;2300-2311.
23. Harty T.P., Manis P.B. Kinetic analysis of glycine receptor currents in ventral cochlear nucleus. J. Neurophysiol. 79:(4):1998;1891-1901.
24. Hutson K.A., Morest D.K. Fine structure of cell clusters in the cochlear nerve root: stellate, granule and mitt cells offer insights into the synaptic circuitry of local circuit neurons. J. Comp. Neurol. 371:1996;397-414.
25. Juiz J.M., Helfert R.H., Bonneau J.M., Wenthold R.J., Altschuler R.A. Three classes of inhibitory amino acid terminals in the cochlear nucleus of the guinea pig. J. Comp. Neurol. 373:1996;11-26.
26. Juiz J.M., Helfert R.H., Bonneau J.M., Campos M.L., Altschuler R.A. Distribution of glycine and GABA immunoreactivities in the cochlear nucleus: quantitative patterns of putative inhibitory inputs on three cell types. J. Hirnforschung. 37:1996;561-574.
27. Kakehata S., Nakagawa T., Takasaka T., Akaike N. Glycine response in isolated dorsal cochlear nucleus of C57BL/6J mouse. Brain Res. 574:1992;21-25.
28. Kolston J., Osen K.K., Hackney C.M., Ottersen O.P., Storm-Mathissen J. An atlas of glycine and GABA-like immunoreactivity and colocalization in the cochlear nuclear complex of the guinea pig. Anat. Embryol. 186:1992;443-465.
29. Kuhse J., Schmieden V., Betz H. Identification and functional expression of a novel ligand binding subunit of the inhibitory glycine receptor. J. Biol. Chem. 265:1990;22317-22320.
30. Kuhse J., Schmieden V., Betz H. A single amino acid exchange alters the pharmacology of neonatal rat glycine receptor subunit. Neuron. 5:1990;867-873.
31. Kungel M., Friauf E. Physiology and pharmacology of native glycine receptors in developing rat auditory brainstem neurons. Dev. Brain Res. 102:1997;157-165.
32. Malosio M.-L., Pouey B.M., Kuhse J., Betz H. Widespread expression of glycine receptor subunit mRNAs in the adult and developing rat brain. EMBO J. 10:1991;2401-2409.
33. Martin M.R., Dickson J.W., Fex J. Bicuculline, strychnine and depressant amino acid responses in the anteroventral cochlear nucleus of the cat. Neuropharmacology. 21:1982;201-207.
34. Moore, J.K., 1986. Cochlear nuclei: relationship to the auditory nerve. In: Altschuler, R.A., Hoffman, D.W., Bobbin, R.P. (Eds.), Neurobiology of Hearing: The Cochlea. Raven Press, New York, NY, pp. 283-301.
35. Oertel, D., Wickesberg, R.E., 1993. Glycinergic inhibition in the cochlear nuclei: evidence for tuberculoventral neurons being glycinergic. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A., Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 225-237.
36. Ostapoff E.M., Benson C.G., Saint Marie R.L. GABA- and glycine-immunoreactive projections from the superior olivary complex to the cochlear nucleus in guinea pig. J. Comp. Neurol. 381:1997;500-512.
37. Pfeiffer F., Simler R., Grenningloh G., Betz H. Monoclonal antibodies and peptide mapping reveal structural similarities between the subunits of the glycine receptor of rat spinal cord. Proc. Natl. Acad. Sci. USA. 81:1984;7224-7227.
38. Potashner, S.J., Benson, C.G., Ostapoff, E.-M., Lindberg, N., Morest, D.K., 1993. Glycine and GABA: transmitter candidates of projections descending to the cochlear nucleus. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A., Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 195-210.
39. Pribilla I., Takagi T., Langosch D., Bormann J., Betz H. The atypical M2 segment of the beta subunit confers picrotoxin resistance to the inhibitory glycine receptor channels. EMBO J. 11:1992;4305-4311.
40. Raman I.M., Trussell L.O. The kinetics of the response to glutamate and kainate in neurons of the avian cochlear nucleus. Neuron. 9:1992;173-186.
41. Sanes D.H., Geary W.A., Wooten G.F., Rubel E.W. Quantitative distribution of the glycine receptor in the auditory brain stem of the gerbil. J. Neurosci. 7:1987;3793-3802.
42. Sato K., Zhang J.H., Saika T., Sato M., Tada K., Tohyama M. Localization of glycine receptor α1 subunit mRNA-containing neurons in the rat brain: an analysis using in situ hybridization histochemistry. Neuroscience. 43:1991;381-395.
43. Sato K., Kiyama H., Tohyama M. Regional distribution of cells expressing glycine receptor α2 subunit mRNA in the rat brain. Brain Res. 590:1992;95-108.
44. Sato K., Kuriyama H., Altschuler R.A. Expression of glycine receptor subunits in the cochlear nucleus and superior olivary complex using non-radioactive in situ hybridization. Hear. Res. 91:1995;7-18.
45. Suneja S.K., Benson C.G., Potashner S.J. Glycine receptors in adult guinea pig brain stem auditory nuclei: regulation after unilateral cochlear ablation. Exp. Neurol. 154:1998;473-488.
46. Trussell L.O. Synaptic mechanisms for coding timing in auditory neurons. Annu. Rev. Physiology. 61:1999;477-496.
47. Trussell L.O., Fischbach G.D. Glutamate receptor desensitization and its role in synaptic transmission. Neuron. 3:1989;209-218.
48. Van den Pol A.N., Gorcs T. Glycine and glycine receptor immunoreactivity in brain and spinal cord. J. Neurosci. 8:1988;472-492.
49. Wenthold, R.J., 1991. Neurotransmitters of brainstem auditory nuclei. In: Altschuler, R.A., Bobbin, R.P., Clopton, B.M., Hoffman, D.W. (Eds.), Neurobiology of Hearing: The Central Auditory System. Raven Press, New York, NY, pp. 121-140.
50. Wenthold, R.J., Hunter, C., 1990. Immunocytochemistry of glycine and GABA receptors in the central auditory system. In: Ottersen, O.P., Storm-Mathissen, J. (Eds.), Glycine Neurotransmission. Wiley and Sons, Chichester, UK, pp. 391-416.
51. Wenthold R.J., Parakkal M.H., Oberdorfer M.D., Altschuler R.A. Glycine receptor immunoreactivity in the ventral cochlear nucleus of the guinea pig. J. Comp. Neurol. 276:1988;423-435.
52. Wickesberg, R.E., Oertel, D., 1993. Intrinsic connection in the cochlear nuclear complex studied in vitro and in vivo. In: Merchan, M.A., Juiz, J.M., Godfrey, D.A., Mugniani, E. (Eds.), The Mammalian Cochlear Nucleus: Organization and Function. Plenum Press, New York, NY, pp. 77-90.
53. Wu S.H., Oertel D. Inhibitory circuitry in the ventral cochlear nucleus is probably mediated by glycine. J. Neurosci. 6:1986;2691-2706.
54. 3H] strychnine. J. Neurosci. 1:1981;532-547.