Abstract
The action of the medial olivocochlear system (MOCS) in the auditory periphery is well established and is described in detail elsewhere in this volume (Guinan, Chap. 3; Sewell, Chap. 4; Katz et al., Chap. 5). The major peripheral effect of activation of the MOCS is a reduction in gain of the outer hair cell (OHC) cochlear amplifier and a consequent reduction in sensitivity of the primary afferent neurons to tones at their most sensitive, or characteristic frequency (CF).
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References
Benson TE, Brown MC (1990) Synapses formed by olivocochlear axon branches in the mouse cochlear nucleus. J Comp Neurol 295:52–70
Benson TE, Berglund AM, Brown MC (1996) Synaptic input to cochlear nucleus dendrites that receive medial olivocochlear synapses. J Comp Neurol 365:27–41
Brown MC (1993) Fiber pathways and branching patterns of biocytin-labeled olivocochlear neurons in the mouse brainstem. J Comp Neurol 337:600–613
Brown MC, Vetter DE (2009) Olivocochlear neuron central anatomy is normal in alpha9 knockout mice. J Assoc Res Otolaryngol 10:64–75
Brown MC, Liberman MC, Benson TE, Ryugo DK (1988) Brainstem branches from olivocochlear axons in cats and rodents. J Comp Neurol 278:591–603
Brown MC, Pierce S, Berglund AM (1991) Cochlear-nucleus branches of thick (medial) olivocochlear fibers in the mouse: a cochleotopic projection. J Comp Neurol 303:300–315
Comis SD, Whitfield IC (1968) Influence of centrifugal pathways on unit activity in the cochlear nucleus. J Neurophysiol 31:62–68
Desmedt JE (1962) Auditory-evoked potentials from cochlea to cortex as influenced by activation of the olivocochlear bundle. J Acoust Soc Am 34:1478–1496
Desmedt JE, Robertson D (1975) Ionic mechanism of the efferent olivo-cochlear inhibition studied by cochlear perfusion in the cat. J Physiol 247:407–428
Ebert U (1996) Noradrenalin enhances the activity of cochlear nucleus neurons in the rat. Eur J Neurosci 8:1306–1314
Fex J (1967) Efferent inhibition in the cochlea related to hair-cell dc activity: study of postsynaptic activity of the crossed olivocochlear fibres in the cat. J Acoust Soc Am 41:666–675
Fujino K, and Oertel D (2001) Cholinergic modulation of stellate cells in the mammalian ventral cochlear nucleus. J Neurosci 21:7372–7383
Kawase T, Delgutte B, Liberman MC (1993) Antimasking effects of the olivocochlear reflex. II. Enhancement of auditory-nerve response to masked tones. J Neurophysiol 70:2533–2549
Klepper A, Herbert H (1991) Distribution and origin of noradrenergic and serotonergic fibers in the cochlear nucleus and inferior colliculus of the rat. Brain Res 557:190–201
Koerber KC, Pfeiffer RR, Warr WB, Kiang NY (1966) Spontaneous spike discharges from single units in the cochlear nucleus after destruction of the cochlea. Exp Neurol 16:119–130
May BJ, Prosen CA, Weiss D, Vetter D (2002) Behavioral investigation of some possible effects of the central olivocochlear pathways in transgenic mice. Hear Res 171:142–157
May BJ, Budelis J, Niparko JK (2004) Behavioral studies of the olivocochlear efferent system: learning to listen in noise. Arch Otolaryngol Head Neck Surg 130:660–664
Mulders WH, Robertson D (2000) Effects on cochlear responses of activation of descending pathways from the inferior colliculus. Hear Res 149:11–23
Mulders WH, Robertson D (2001) Origin of the noradrenergic innervation of the superior olivary complex in the rat. J Chem Neuroanat 21:313–322
Mulders WH, Robertson D (2005) Catecholaminergic innervation of guinea pig superior olivary complex. J Chem Neuroanat 30:230–242
Mulders WH, Winter IM, Robertson D (2002) Dual action of olivocochlear collaterals in the guinea pig cochlear nucleus. Hear Res 174:264–280
Mulders WH, Paolini AG, Needham K, Robertson D (2003) Olivocochlear collaterals evoke excitatory effects in onset neurones of the rat cochlear nucleus. Hear Res 176:113–121
Mulders WH, Harvey AR, Robertson D (2007) Electrically evoked responses in onset chopper neurons in guinea pig cochlear nucleus. J Neurophysiol 97:3288–3297
Mulders WH, Seluakumaran K, Robertson D (2008) Effects of centrifugal pathways on responses of cochlear nucleus neurons to signals in noise. Eur J Neurosci 27:702–714
Patuzzi R, Rajan R (1992) Additivity of threshold elevations produced by disruption of outer hair cell function. Hear Res 60:165–177
Patuzzi R, Johnstone BM, Sellick PM (1984) The alteration of the vibration of the basilar membrane produced by loud sound. Hear Res 13:99–100
Pickles JO (1976a) The noradrenaline-containing innervation of the cochlear nucleus and the detection of signals in noise. Brain Res 105:591–596
Pickles JO (1976b) Role of centrifugal pathways to cochlear nucleus in determination of critical bandwidth. J Neurophysiol 39:394–400
Pickles JO, Comis SD (1973) Role of centrifugal pathways to cochlear nucleus in detection of signals in noise. J Neurophysiol 36:1131–1137
Pressnitzer D, Meddis R, Delahaye R, Winter IM (2001) Physiological correlates of comodulation masking release in the mammalian ventral cochlear nucleus. J Neurosci 21:6377–6386
Rajan R, Patuzzi RB (1992) Additivity of threshold losses produced by acute acoustic trauma. Hear Res 60:216–230
Seluakumaran K, Mulders WH, Robertson D (2008a) Effects of medial olivocochlear efferent stimulation on the activity of neurons in the auditory midbrain. Exp Brain Res 186:161–174
Seluakumaran K, Mulders WH, Robertson D (2008b) Unmasking effects of olivocochlear efferent activation on responses of inferior colliculus neurons. Hear Res 243:35–46
Sewell WF (1984) The relation between the endocochlear potential and spontaneous activity in auditory nerve fibres of the cat. J Physiol 347:685–696
Sherriff FE, Henderson Z (1994) Cholinergic neurons in the ventral trapezoid nucleus project to the cochlear nuclei in the rat. Neuroscience 58:627–633
Shore SE, El Kashlan H, Lu J (2003) Effects of trigeminal ganglion stimulation on unit activity of ventral cochlear nucleus neurons. Neuroscience 119:1085–1101
Starr A, Wernick JS (1968) Olivocohlear bundle stimulation: effect on spontaneous and tone-evoked activities of single units in cat cochlear nucleus. J Neurophysiol 31:549–564
Thompson AM, Moore KR, Thompson GC (1995) Distribution and origin of serotoninergic afferents to guinea pig cochlear nucleus. J Comp Neurol 351:104–116
Verhey JL, Pressnitzer D, Winter IM (2003) The psychophysics and physiology of comodulation masking release. Exp Brain Res 153:405–417
Wiederhold ML (1970) Variations in the effects of electric stimulation of the crossed olivocochlear bundle on cat single auditory-nerve-fiber responses to tone bursts. J Acoust Soc Am 48:966–977
Wiederhold ML, Kiang NY (1970) Effects of electric stimulation of the crossed olivocochlear bundle on single auditory-nerve fibers in the cat. J Acoust Soc Am 48:950–965
Winslow RL, Sachs MB (1987) Effect of electrical stimulation of the crossed olivocochlear bundle on auditory nerve response to tones in noise. J Neurophysiol 57:1002–1021
Winter IM, Robertson D, Cole KS (1989) Descending projections from auditory brainstem nuclei to the cochlea and cochlear nucleus of the guinea pig. J Comp Neurol 280:143–157
Acknowledgments
This work was supported by grants from the NHMRC (Australia), the Medical Heath and Research Infrastructure Fund, The Royal National Institute for Deaf People, and The University of Western Australia.
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Robertson, D., Mulders, W.H.A.M. (2011). Central Effects of Efferent Activation. In: Ryugo, D., Fay, R. (eds) Auditory and Vestibular Efferents. Springer Handbook of Auditory Research, vol 38. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-7070-1_10
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