Abstract
The spiral ganglion cells provide the afferent innervation of the hair cells of the organ of Corti. Ninety-five percent of these cells (termed type I spiral ganglion neurones) are in synaptic contact with the inner hair cells, whereas about 5% of them are type II cells, which are responsible for the sensory innervation of the outer hair cells. To understand the function of the spiral ganglion neurones, it is important to explore their membrane properties, understand their activity patterns and describe the variety of ionic channels determining their behaviour. In this review, a brief description is given of the various experimental methods that allow the investigation of the spiral ganglion cells, followed by the discussion of their action potential firing patterns and ionic conductances. The presence, distribution and significance of the K+ currents of the spiral ganglion cells are specifically addressed, along with the introduction of the putative subunit compositions of the relevant voltage-gated K+ channels.
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References
Rasmussen GL (1946) The olivary peduncle and the other fiber projections of the superior olivary complex. J Comp Neurol 84:141
Kellerhals B, Engstrom H, Ades HW (1967) Die Morphologie des Ganglion spirale cochleae. Acta Otolaryngol 226:1–78
Spoendlin H (1971) Degeneration behaviour of the cochlear nerve. Arch Klin Exp Ohren Nasen Kehlkopfheilk 200:275–291
Spoendlin H (1981) Differentiation of cochlear afferent neurons. Acta Otolaryngol 91:451–456
Morrison D, Schindler RA, Wersäll J (1975) Quantitative analysis of the afferent innervation of the organ of Corti in guinea pig. Acta Otolaryngol 79:11–23
Ota CY, Kimura RS (1980) Ultrastructural study of the human spiral ganglion. Acta Otolaryngol 89:53–62
Ryan AF, Schwartz IR (1983) Preferential amino acid uptake identifies type II spiral ganglion neurons in the gerbil. Hear Res 9:173–194
Spoendlin H (1969) Innervation patterns in the organ of Corti of the cat. Acta Otolaryngol 67:239–254
Spoendlin H (1972) Innervation densities of the cochlea. Acta Otolaryngol 73:235–248
Spoendlin H (1979) Neural connections of the outer hair cell system. Acta Otolaryngol 87:381–387
Robertson D (1984) Horseradish peroxidase injection of physiologically characterized afferent and efferent neurones in the guinea pig spiral ganglion. Hear Res 15:113–121
Berglund AM, Ryugo DK (1987) Hair cell innervation by spiral ganglion neurons in the mouse. J Comp Neurol 255:560–570
Brown MC (1987) Morphology of labeled afferent fibers in the guinea pig cochlea. J Comp Neurol 260:591–604
Echeteler SM (1992) Developmental segregation in the afferent projections to mammalian auditory hair cells. Proc Natl Acad Sci USA 89:6324–6327
Robertson D, Sellcik PM, Patuzzi R (1999) The continuing search for outer hair cell afferents in the guinea pig spiral ganglion. Hear Res 136:151–158
Hudspeth AJ, Jacobs R (1979) Stereocilia mediate transduction in vertebrate hair cells. Proc Natl Acad Sci USA 76:1506–1509
Hudspeth AJ (1985) The cellular basis of hearing: the biophysics of hair cells. Science 230:745–752
Kros CJ, Crawford AC (1990) Potassium currents in inner hair cells isolated from the guinea-pig cochlea. J Physiol 421:263–291
Roberts WM, Jacobs RA, Hudspeth AJ (1990) Colocalization of ion channels involved in frequency selectivity and synaptic transmission at presynaptic active zones of hair cells. J Neurosci 10:3664–3684
Zhang SY, Robertson D, Yates G, Everett A (1999) Role of L-type Ca2+ channels in transmitter release from mammalian inner hair cells. I. Gross sound-evoked potentials. J Neurophysiol 82:3307–3315
Godfrey DA, Carter JA, Berger SJ, Matschinsky FM (1976) Levels of putative transmitter amino acids in the guinea pig cochlea. J Histochem Cytochem 24:468–470
Altschuler RA, Sheridan CE, Horn JW, Wenthold RJ (1989) Immunocytochemical localization of glutamate immunoreactivity in the guinea pig cochlea. Hear Res 42:167–173
Drescher MJ, Drescher DG (1992) Glutamate, of the endogenous primary alpha-amino acid, is specifically released from hair cells by elevated extracellular potassium. J Neurochem 59:93–98
Niedzielski AS, Wenthold RJ (1995) Expression of AMPA, kainate, and NMDA receptor subunits in cochlear and vestibular ganglia. J Neurosci 13:3496–3509
Matsubara A, Laake JH, Davanger S, Usami S, Ottersen OP (1996) 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 16:4457–4467
Ruel J, Chen C, Pujol R, Bobbin RP, Puel JL (1999) AMPA-preferring glutamate receptors in cochlear physiology of adult guinea-pig. J Physiol 518:667–680
Glowatzki E, Fuchs PA (2002) Transmitter release at the hair cell ribbon synapse. Nature Neurosci 5:147–154
Saffieddine S, Eybalin M (1992) Co-expression of NMDA and AMPA/kainate receptor mRNAs in cochlear neurones. Neuroreport 3:1145–1148
Zheng J, Shen W, He DZ, Long KB, Madison LD, Dallos P (2000) Prestin is the motor protein of cochlear outer hair cells. Nature 405:149–155
Dallos P, Corey ME (1991) The role of outer hair cell motility in cochlear tuning. Curr Opin Neurobiol 1:215–220
Usami S, Osen KK, Zhang N, Ottersen OP (1992) Distribution of glutamate-like and glutamine-like immunoreactivities in the rat organ of Corti: a light microscopic and semiquantitative electron microscopic analysis with a note on the localization of aspartate. Exp Brain Res 91:1–11
Kuriyama H, Albin RL, Altschuler RA (1993) Expression of NMDA receptor mRNA in the rat cochlea. Hear Res 69:215–220
Kuriyama H, Jenkins O, Altschuler RA (1994) Immunocytochemical localization of AMPA selective glutamate receptor subunits in the rat cochlea. Hear Res 80:233–240
Mott JB, Norton SJ, Neely ST, Warr WB (1989) Changes in spontaneous otoacoustic emissions produced by acoustic stimulation of the contralateral ear. Hear Res 38:229–242
Collet L, Kemp DT, Veuillet E, Duclaux R, Moulin A, Morgon A (1990) Effect of contralateral auditory stimuli on active cochlear micro-mechanical properties in human subjects. Hear Res 43:251–261
Whitehead ML, Martin GK, Lonsbury-Martin BL (1991) Effects of crossed acoustic reflex on distortion-product otoacoustic emissions in awake rabbits. Hear Res 51:55–72
Bobbin RP, Konishi T (1971) Acetylcholine mimics crossed olivocochlear bundle stimulation. Nat New Biol 231:222–223
Warr WB (1975) Olivocochlear and vestibular efferent neurons of the feline brain stem: their location, morphology and number determined by retrograde axonal transport and acetylcholinesterase histochemistry. J Comp Neurol 161:159–181
Robertson D, Johnstone BM (1978) Efferent transmitter substance in the mammalian cochlea: single neuron support for acetylcholine. Hear Res 1:31–34
Altschuler RA, Kachar B, Rubio JA, Parakkal MH, Fex J (1985) Immunocytochemical localization of choline acetyltransferase-like immunoreactivity in the guinea pig cochlea. Brain Res 338:1–11
Eybalin M, Pujol R (1987) Choline acetyltransferase (ChAT) immunoelectron microscopy distinguishes at least three types of efferent synapses in the organ of Corti. Exp Brain Res 65:261–270
Eybalin M, Parnaud C, Geffard M, Pujol R (1988) Immunoelectron microscopy identifies several types of GABA-containing efferent synapses in the guinea-pig organ of Corti. Neuroscience 24:29–38
Reale RA, Imig TJ (1980) Tonotopic organization in auditory cortex of the cat. J Comp Neurol 192:265–291
Lauter JL, Herscovitch P, Formby C, Raichle ME (1985) Tonotopic organization in human auditory cortex revealed by positron emission tomography. Hear Res 20:199–205
Romand R, Romand MR (1985) Qualitative and quantitative observations of spiral ganglion development of the rat. Hear Res 18:111–120
Simmons DD, Manson-Gieske L, Hendrix TW, Morris K, Williams SJ (1991) Postnatal maturation of spiral ganglion neurons: a horseradish peroxidase study. Hear Res 55:81–91
Echeteler SM, Nofsinger YC (2000) Development of ganglion cell topography in the postnatal cochlea. J Comp Neurol 425:436–446
Anniko M (1983) Early development and maturation of the spiral ganglion. Acta Otolaryngol 95:263–276
Bakondi G, Pór Á, Kovács I, Szűcs G, Rusznák Z (2008) Voltage-gated K+ channel (Kv) subunit expression of the guinea pig spiral ganglion cells studied in a newly developed cochlear free-floating preparation. Brain Res 1210:148–162
Liberman CM, Oliver ME (1984) Morphometry of intracellularly labeled neurons of the auditory nerve: correlations with functional properties. J Comp Neurol 223:163–176
Montero C (2003) The antigen–antibody reaction in immunohistochemistry. J Histochem Cytochem 51:1–4
Mo ZL, Davis RL (1997) Endogenous firing patterns of murine spiral ganglion neurons. J Neurphysiol 77:1294–1305
Jagger DJ, Robertson D, Housley GD (2000) A technique for slicing the rat cochlea around the onset of hearing. J Neurosci Meth 104:77–86
Chen WC, Davis RL (2006) Voltage-gated and two-pore-domain potassium channels in murine spiral ganglion neurons. Hear Res 222:89–99
Xie D, Hu P, Xiao Z, Wu W, Chen Y, Xia K (2007) Subunits of voltage-gated calcium channels in murine spiral ganglion cells. Acta Otolaryngol 127:8–12
Spoendlin H (1985) Anatomy of cochlear innervation. Am J Otolaryngol 6:453–467
Perkins RE, Morest DK (1975) A study of cochlear innervation patterns in cats and rats with the Golgi method and Nomarski optics. J Comp Neurol 163:129–158
Liberman MC (1982) The cochlear frequency map for the cat: labelling auditory-nerve fibers of known characteristic frequency. J Acoust Soc Am 72:1441–1449
Lin X (1997) Action potentials and underlying voltage-dependent currents studied in cultured spiral ganglion neurons of the postnatal gerbil. Hear Res 108:157–179
Liberman MC, Dodds LW, Pierce S (1990) Afferent and efferent innervation of the cat cochlea: quantitative analysis with light and electron microscopy. J Comp Neurol 301:443–460
Echteler SM (1992) Developmental segregation in the afferent projections to mammalian auditory hair cells. Proc Natl Acad Sci USA 89:6324–6327
Sando I (1965) The anatomical interrelationships of the cochlear nerve fibers. Acta Otolaryngol 59:417
Fischer FP (1998) Hair cell morphology and innervation in the basilar papilla of the emu (Dromaius novaehollandiae). Hear Res 121:112–124
Brown MC (1987) Morphology of labeled afferent fibers in the guinea pig cochlea. J Comp Neurol 260:591–604
Fechner FP, Burgess BJ, Adams JC, Liberman MC, Nadol JB Jr (1998) Dense innervation of Deiters’ and Hensen’s cells persists after chronic deefferentation of guinea pig cochleas. J Comp Neurol 400:299–309
Berglund AM, Brown MC (1994) Central trajectories of type II spiral ganglion cells from various cochlear regions in mice. Hear Res 75:121–130
Fechner FP, Nadol JJ, Burgess BJ, Brown MC (2001) Innervation of supporting cells in the apical turns of the guinea pig cochlea is from type II afferent fibers. J Comp Neurol 429:289–298
Dulon D, Moataz R, Mollard P (1993) Characterization of Ca2+ signals generated by extracellular nucleotides in supporting cells of the organ of Corti. Cell Calcium 14:245–254
Dulon D, Blanchet C, Lafflon E (1994) Photo-released intracellular Ca2+ evokes reversible mechanical responses in supporting cells of the guinea-pig organ of Corti. Biochem Biophys Res Comm 201:1263–1269
Sugasawa M, Erostegui C, Blanchet C, Dulon D (1996) ATP activates a cation conductance and Ca2+-dependent Cl− conductance in Hensen cells of guinea pig cochlea. Am J Physiol 271:1817–1827
Santos-Sacchi J (1993) Voltage-dependent ionic conductances of type I spiral ganglion cells from the guinea pig inner ear. J Neurosci 13:3599–3611
Kimura RS, Bongiorno CL, Iverson NA (1987) Synapses and ephapses in the spiral ganglion. Acta Otolaryngol Suppl 438:1–18
Kimura RS, Ota CY, Takahashi T (1979) Nerve fiber synapses on spiral ganglion cells in the human cochlea. Ann Otol Rhinol Laryngol Suppl 62:1–17
Arnold W (1987) Myelination of the human spiral ganglion. Acta Otolaryngol Suppl 436:76–84
Szabó ZS, Harasztosi CS, Sziklai I, Szűcs G, Rusznák Z (2002) Ionic currents determining the membrane characteristics of type I spiral ganglion neurons of the guinea pig. Eur J Neurosci 16:1887–1895
Szabó ZS, Harasztosi CS, Szűcs G, Sziklai I, Rusznák Z (2003) A detailed procedure and dissection guide for the isolation of spiral ganglion cells of the guinea pig for electrophysiological experiments. Brain Res Protoc 10:139–147
Chen C (1997) Hyperpolarization-activated current (I h) in primary auditory neurons. Hear Res 110:179–190
Robertson D (1976) Possible reaction between structure and spike shapes of neurones of the guinea pig cochlear ganglion. Brain Res 106:487–496
Yates GK, Robertson D, Johnstone BM (1985) Very rapid adaptation in the guinea pig auditory nerve. Hear Res 17:1–12
Romand R, Romand MR, Mulle C, Marty R (1980) Early stages of myelination in the spiral ganglion cells of the kitten during development. Acta Otolaryngol 90:391–397
Romand R, Romand MR (1986) Perinatal growth of spiral ganglion cells in the kitten. Hear Res 21:161–165
Romand MR, Romand R (1987) The ultrastructure of spiral ganglion cells in the mouse. Acta Otolaryngol 104:29–39
Romand MR, Romand R (1990) Development of spiral ganglion cells in mammalian cochlea. J Electron Microsc 15:144–154
Goycoolea MV, Stypulkowski P, Muchow DC (1990) Ultrastructural studies of the peripheral extensions (dendrites) of type I ganglion cells in the cat. Laryngoscope 100:19–24
Romand R, Romand MR (1985) Qualitative and quantitative observations of spiral ganglion development in the rat. Hear Res 18:111–120
Jagger DJ, Housley GD (2003) Membrane properties of type II spiral ganglion neurones identified in a neonatal rat cochlear slice. J Physiol 552:525–533
Nadol JB Jr, Burgess B, Reissner C (1990) Morphometric analysis of normal human spiral ganglion cells. Ann Otol Rhinol Laryngol 99:340–348
Anniko M, Arnold W, Stigbrand T, Ström A (1995) The human spiral ganglion. ORL J Otorhinolaryngol Relat Spec 57:68–77
Hafidi A, Despres G, Romand R (1993) Ontogenesis of type II spiral ganglion neurons during development: peripherin immunohistochemistry. Int J Dev Neurosci 11:507–512
Hafidi A (1998) Peripherin-like immunoreactivity in type II spiral ganglion cell body and projections. Brain Res 805:181–190
Mou K, Adamson CL, Davis RL (1998) Time-dependence and cell-type specificity of synergistic neurotrophin actions on spiral ganglion neurons. J Comp Neurol 402:129–139
Reid MA, Flores-Otero J, Davis RL (2004) Firing patterns of type II spiral ganglion neurons in vitro. J Neurosci 24:733–742
Hsu Y, Firestein BL, Davis RL (2002) Differential distribution of membrane-associated guanylate kinases (MAGUKs) in type I and type II spiral ganglion neurons. Assoc Res Otolaryngol 25:410
Jagger DJ, Housley GD (2002) A-type potassium currents dominate repolarisation of neonatal rat primary auditory neurones in situ. Neuroscience 109:169–182
Malgrange B, Rigo JM, Lefebvre PP, Coucke P, Goffin F, Xhauflaire G, Belachew S, Van De Water TR, Moonen G (1997) Diazepam-insensitive GABAA receptors on postnatal spiral ganglion neurones in culture. NeuroReport 8:591–596
Lin X, Chen S, Chen P (2000) Activation of metabotropic GABAB receptors inhibited glutamate responses in spiral ganglion neurons of mice. NeuroReport 11:957–961
Cho H, Harada N, Yamashita T (1997) Extracellular ATP-induced Ca2+ mobilization of type I spiral ganglion cells from the guinea pig cochlea. Acta Otolaryngol 117:545–552
Salih SG, Housley GD, Raybould NP, Thorne PR (1999) ATP-gated ion channel expression in primary auditory neurones. NeuroReport 10:2579–2586
Rome C, Luo D, Dulon D (1999) Muscarinic receptor-mediated calcium signalling in spiral ganglion neurons of the mammalian cochlea. Brain Res 846:196–203
Adamson CL, Reid MA, Mo ZL, Bowne-English J, Davis RL (2002) Firing features and potassium channel content of murine spiral ganglion neurons vary with cochlear location. J Comp Neurol 447:331–350
Evans EF (1972) The frequency response and other properties of single fibres in the guinea-pig cochlear nerve. J Physiol 226:263–287
Liberman MC (1978) Auditory-nerve response from cats raised in a low-noise chamber. J Acoust Soc Am 63:442–455
Bobbin RP (1979) Glutamate and aspartate mimic the afferent transmitter of the cochlea. Exp Brain Res 34:389–393
Sewell WF (1984) The relation between the endocochlear potential and spontaneous activity in auditory nerve fibres of the cat. J Physiol 347:685–696
Kawase T, Liberman MC (1992) Spatial organisation of the auditory nerve according to spontaneous discharge rate. J Comp Neurol 319:312–318
Lin X, Chen S (2000) Endogenously generated spontaneous spiking activities recorded from postnatal spiral ganglion neurons in vitro. Dev Brain Res 119:297–305
Robertson D, Paki B (2002) Role of L-type Ca2+ channels in transmitter release from mammalian inner hair cells. II. Single-neuron activity. J Neurophysiol 87:2734–2740
Cousillas H, Cole KS, Johnstone BM (1988) Effect of spider venom on cochlear nerve activity consistent with glutaminergic transmission at hair cell-afferent dendrite synapse. Hear Res 36:213–220
Puel JL, Bobbin RP, Fallon M (1989) Suppression of auditory nerve activity in the guinea pig cochlea by 1-(ρ-bromobenzoyl)-piperazine-2,3-dicarboxylic acid. Brain Res 487:9–15
Robertson D (1985) Brainstem location of efferent neurons projecting to the guinea pig cochlea. Hear Res 20:79–84
Zhou Z, Liu Q, Davis RL (2005) Complex regulation of spiral ganglion neuron firing patterns by neurotrophin-3. J Neurosci 25:7558–7566
Hapner SJ, Boeshore KL, Large TH, Lefcort F (1998) Neural differentiation promoted by truncated trkC receptors in collaboration with p75(NTR). Dev Biol 201:90–100
Adamson CL, Reid MA, Davis RL (2002) Opposite actions of brain-derived neurotrophic factor and neurotrophin-3 on firing features and ion channel composition of murine spiral ganglion neurons. J Neurosci 22:1385–1396
Malgrange B, Rogister B, Lefebvre PP, Mazy-Servais C, Welcher AA, Bonnet C, Hsu R-Y, Rigo J-M, Van De Water TR, Moonen G (1998) Expression of growth factors and their receptors in the postnatal rat cochlea. Neurochem Res 23:1133–1138
Luo L, Koutnouyan H, Baird A, Ryan AF (1993) Acidic and basic FGF mRNA expression in the adult and developing rat cochlea. Hear Res 69:182–193
Marzella PL, Gillespie LN, Clark GM, Bartlett PF, Kilpatrick TJ (1999) The neurotrophins act synergistically with LIF and members of the TGF-β superfamily to promote the survival of spiral ganglia neurons in vitro. Hear Res 138:73–80
Hossain WA, Morest DK (2000) Fibroblast growth factors (FGF-1, FGF-2) promote migration and neurite growth of mouse cochlear ganglion cells in vitro: immunocytochemistry and antibody perturbation. J Neurosci Res 62:40–55
Gillespie LN, Clark GM, Bartlett PF, Marzella PL (2001) LIF is more potent than BDNF in promoting neurite outgrowth of mammalian auditory neurons in vitro. NeuroReport 12:275–279
Ernfors P, Van De Water T, Loring J, Jaenisch R (1995) Complementary roles of BDNF and NT-3 in vestibular and auditory development. Neuron 14:1153–1164
Moser T, Beutner D (2000) Kinetics of exocytosis and endocytosis at the cochlear inner hair cell afferent synapse of the mouse. Proc Natl Acad Sci USA 97:883–888
Dodson PD, Forsythe ID (2004) Presynaptic K+ channels: electrifying regulators of synaptic terminal excitability. Trends Neurosci 27:210–217
García-Díaz JF (1999) Development of a fast transient potassium current in chick cochlear ganglion neurons. Hear Res 135:124–134
Lin X, Chen S, Tee D (1998) Effects of quinine on the excitability and voltage-dependent currents of isolated spiral ganglion neurons in culture. J Neurophysiol 79:2503–2512
Fernandez FR, Morales E, Rashid AJ, Dunn RJ, Turner RW (2003) Inactivation of Kv3.3 potassium channels in heterologous expression systems. J Biol Chem 278:40890–40898
Mo ZL, Adamson CL, Davis RL (2002) Dendrotoxin-sensitive K+ currents contribute to accommodation in murine spiral ganglion neurons. J Physiol 542:763–778
Allen ML, Koh DS, Tempel BL (1998) Cyclic cAMP regulates potassium channel expression in C6 glioma by destabilizing Kv1.1 mRNA. Proc Natl Acad Sci USA 95:7693–7698
Hopkins WF (1998) Toxin and subunit specificity of blocking affinity of three peptide toxins for heteromultimeric, voltage-gated potassium channels expressed in Xenopus oocytes. J Pharmacol Exp Ther 285:1051–1060
Smart SL, Bosma MM, Tempel BL (1997) Identification of the delayed rectifier potassium channel, Kv1.6, in cultured astrocytes. Glia 20:127–134
Harvey AL (2001) Twenty years of dendrotoxins. Toxicon 39:15–26
Grissmer S, Nguyen AN, Aiyar J, Hanson DC, Mather RJ, Gutman GA, Karmilowicz MJ, Auperin DD, Chandy KG (1994) Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably expressed in mammalian cell lines. Mol Pharmacol 45:1227–1234
Hopkins WF, Allen ML, Houamed KM, Tempel BL (1994) Properties of voltage-gated K+ currents expressed in Xenopus oocytes by mKv1.1, mKv1.2 and their heteromultimers as revealed by mutagenesis of the dendrotoxin-binding site in mKv1.1. Pflügers Arch 428:382–390
Southan AP, Robertson B (2000) Electrophysiological characterization of voltage-gated K+ currents in cerebellar basket and purkinje cells: Kv1 and Kv3 channel subfamilies are present in basket cell nerve terminals. J Neurosci 20:114–122
Bekkers JM, Delaney AJ (2001) Modulation of excitability by alpha-dendrotoxin-sensitive potassium channels in neocortical pyramidal neurons. J Neurosci 21:6553–6560
Manis PB, Marx SO (1991) Outward currents in isolated ventral cochlear nucleus neurons. J Neurosci 11:2865–2880
Brew HM, Forsythe ID (1995) Two voltage-dependent K+ conductances with complementary functions in postsynaptic integration at a central auditory synapse. J Neurosci 15:8011–8022
Rathouz M, Trussel L (1998) Characterization of outward currents in neurons of the avian nucleus magnocellularis. J Neurophysiol 80:2824–2835
Brew HM, Hallows JL, Tempel BL (2003) Hyperexcitability and reduced low threshold potassium currents in auditory neurons of mice lacking the channel subunit Kv1.1. J Physiol 548:1–20
Pál B, Rusznák Z, Harasztosi CS, Szűcs G (2004) Depolarization-activated K+ currents of the bushy neurones of the rat cochlear nucleus in a thin brain slice preparation. Acta Physiol Hun 91:83–98
Moore EJ, Hall DB, Narahashi T (1996) Sodium and potassium currents of type I spiral ganglion cells from rat. Acta Otolaryngol 116:552–560
Sheppard DN, Valverde MA, Represa J, Giraldez F (1992) Transient outward currents in cochlear ganglion neurons of the chick embryo. Neuroscience 51:631–639
Valverde MA, Sheppard DN, Represa J, Giraldez F (1992) Development of Na+ - and K+ -currents in the cochlear ganglion of the chick embryo. Neuroscience 51:621–630
Rusznák Z, Forsythe ID, Brew HM, Stanfiled PR (1997) Membrane current influencing action potential latency in granule neurons of the rat cochlear nucleus. Eur J Neurosci 9:2348–2358
Lopez-Barneo J, Llinás R (1988) Electrophysiology of mammalian tectal neurones in vitro. I. Transient ionic conductances. J Neurophysiol 60:853–868
Rogawski MA (1985) The A-current: how ubiquitous a feature of excitable cells is? Trends Neurosci 8:214–219
Mo ZL, Davis RL (1997) Heterogeneous voltage dependence of inward rectifier currents in spiral ganglion neurons. J Neurophysiol 78:3019–3027
Pape H-C, McCormick DA (1989) Noradrenalin and serotonin selectively modulate thalamic burst firing by enhancing a hyperpolarization-activated cation current. Nature 340:715–718
McCormick DA, Huguenard IR (1992) A model of the electrophysiological properties of thalamocortical relay neurons. J Neurophysiol 68:1384–1400
Erickson KR, Ronnekleiv OK, Kelly MJ (1993) Electrophysiology of guinea-pig supraoptic neurones: role of a hyperpolarization-activated cation current in phasic firing. J Physiol 460:407–425
Bal T, McCormick DA (1997) Synchronized oscillations in the inferior olive are controlled by the hyperpolarization-activated cation current Ih. J Neurophysiol 77:3145–3156
McCormick DA, Pape HC (1990) Properties of a hyperpolarization-activated cation current and its role in rhythmic oscillation in thalamic relay neurones. J Physiol 431:291–318
Pál B, Pór Á, Szűcs G, Kovács I, Rusznák Z (2003) HCN channels contribute to the intrinsic activity of cochlear pyramidal cells. Cell Mol Life Sci 60:2189–2199
Hossain WA, Antic SD, Yang Y, Rasband MN, Morest DK (2005) Where is the spike generator of the cochlear nerve? Voltage-gated sodium channels in the mouse cochlea. J Neurosci 25:6857–6868
Couloigner V, Fay M, Djelidi S, Farman N, Escoubet B, Runembert I, Sterkers O, Friedlander G, Ferrary E (2001) Location and function of the epithelial Na channel in the cochlea. Am J Physiol Renal Physiol 280:F214–F222
Zhong SX, Liu ZH (2004) Immunohistochemical localization of the epithelial sodium channel in the rat inner ear. Hear Res 193:1–8
Peng BG, Ahmad S, Chen S, Chen P, Price MP, Lin X (2004) Acid-sensing ion channel 2 contributes a major component to acid-evoked excitatory responses in spiral ganglion neurons and plays a role in noise susceptibility of mice. J Neurosci 24:10167–10175
Hisashi K, Nakagawa T, Yasuda T, Kimitsuki T, Komune S, Komiyama S (1995) Voltage-dependent Ca2+ channels in the spiral ganglion cells of guinea pig cochlea. Hear Res 91:196–201
Yamaguchi K, Ohmori H (1990) Voltage-gated and chemically gated ionic channels in the cultured cochlear ganglion neurone of the chick. J Physiol 420:185–206
Jiménez C, Giraldez F, Represa J, Garcia-Diaz JF (1997) Calcium currents in dissociated cochlear neurons from the chick embryo and their modification by neurotrophin-3. Neuroscience 77:673–682
Lopez I, Ishiyama G, Acuna D, Ishiyama A, Baloh RW (2003) Immunolocalization of voltage-gated calcium channel α1 subunits in the chinchilla cochlea. Cell Tissue Res 313:177–186
Morton-Jones RT, Cannell MB, Jeyakumar LH, Fleischer S, Housley GD (2006) Differential expression of ryanodine receptors in the rat cochlea. Neuroscience 137:275–286
Balaban CD, Zhou J, Li HS (2003) Type 1 vanilloid receptor expression by mammalian inner ear ganglion cells. Hear Res 175:165–170
Zheng J, Dai C, Steyger PS, Kim Y, Vass Z, Ren T, Nuttall AL (2003) Vanilloid receptors in hearing: altered cochlear sensitivity by vanilloids and expression of TRPV1 in the organ of Corti. J Neurophysiol 90:444–445
Kitahara T, Li HS, Balaban CD (2005) Changes in transient receptor potential cation channel superfamily V (TRPV) mRNA expression in the mouse inner ear ganglia after kanamycin challenge. Hear Res 201:132–144
Takumida M, Kubo N, Ohtani M, Suzuka Y, Anniko M (2005) Transient receptor potential channels in the inner ear: presence of transient receptor potential channel subfamily 1 and 4 in the guinea pig inner ear. Acta Otolaryngol 125:929–934
Shen J, Harada N, Kubo N, Liu B, Mizuno A, Suzuki M, Yamashita T (2006) Functional expression of transient receptor potential vanilloid 4 in the mouse cochlea. NeuroReport 17:135–139
Bauer CA, Brozoski TJ, Myers KS (2007) Acoustic injury and TRPV1 expression in the cochlear spiral ganglion. Int Tinnitus J 13:21–28
Hibino H, Horio Y, Fujita A, Inanobe A, Doi K, Gotow T, Uchiyama Y, Kubo T, Kurachi Y (1999) Expression of an inwardly rectifying K+ channel, Kir4.1, in satellite cells of the rat cochlear ganglia. Am J Physiol 277:C638–C644
Rozengurt N, Lopez I, Chiu CS, Kofuji P, Lester HA, Neusch C (2003) Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit. Hear Res 177:71–80
Jin Z, Wei D, Jarlebark L (2006) Developmental expression and localization of KCNJ10 K+ channels in the guinea pig inner ear. NeuroReport 17:475–479
Kanjhan R, Balke CL, Housley GD, Bellingham MC, Noakes PG (2004) Developmental expression of two-pore domain K+ channels, TASK-1 and TREK-1, in the rat cochlea. NeuroReport 15:437–441
Acknowledgements
The authors are indebted to Drs. G. Bakondi and B. Pál for reviewing and commenting on the manuscript. The authors are most grateful to Dr. B. Pál for preparing the hand-drawn illustrations, and to two unnamed reviewers whose professional and helpful suggestions and comments were very useful. This work was supported by grants from the Hungarian Scientific Research Fund (OTKA K-72812, NK-61412).
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Rusznák, Z., Szűcs, G. Spiral ganglion neurones: an overview of morphology, firing behaviour, ionic channels and function. Pflugers Arch - Eur J Physiol 457, 1303–1325 (2009). https://doi.org/10.1007/s00424-008-0586-2
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DOI: https://doi.org/10.1007/s00424-008-0586-2