Interaction of Excitation and Inhibition in Anteroventral Cochlear Nucleus Neurons That Receive Large Endbulb Synaptic Endings

Spherical bushy cells (SBCs) of the anteroventral cochlear nucleus (AVCN) receive their main excitatory input from auditory nerve fibers (ANFs) through large synapses, endbulbs of Held. These cells are also the target of inhibitory inputs whose function is not well understood. The present study examines the role of inhibition in the encoding of low-frequency sounds in the gerbil's AVCN. The presynaptic action potentials of endbulb terminals and postsynaptic action potentials of SBCs were monitored simultaneously in extracellular single-unit recordings in vivo. An input–output analysis of presynaptic and postsynaptic activity was performed for both spontaneous and acoustically driven activity. Two-tone stimulation and neuropharmacological experiments allowed the effects of neuronal inhibition and cochlear suppression on SBC activity to be distinguished. Ninety-one percent of SBCs showed significant neuronal inhibition. Inhibitory sidebands enclosed the high- or low-frequency, or both, sides of the excitatory areas of these units; this was reflected as a presynaptic to postsynaptic increase in frequency selectivity of up to one octave. Inhibition also affected the level-dependent responses at the characteristic frequency. Although in all units the presynaptic recordings showed monotonic rate-level functions, this was the case in only half of the postsynaptic recordings. In the other half of SBCs, postsynaptic inhibitory areas overlapped the excitatory areas, resulting in nonmonotonic rate-level functions. The results demonstrate that the sound-evoked spike activity of SBCs reflects the integration of acoustically driven excitatory and inhibitory input. The inhibition specifically affects the processing of the spectral, temporal, and intensity cues of acoustic signals.

[1]  D. Caspary,et al.  Inhibitory inputs modulate discharge rate within frequency receptive fields of anteroventral cochlear nucleus neurons. , 1994, Journal of neurophysiology.

[2]  P. Manis,et al.  Outward currents in isolated ventral cochlear nucleus neurons , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[3]  R. A. Schmiedt Spontaneous rates, thresholds and tuning of auditory-nerve fibers in the gerbil: Comparisons to cat data , 1989, Hearing Research.

[4]  R. Wenthold,et al.  Glycine immunoreactivity localized in the cochlear nucleus and superior olivary complex , 1987, Neuroscience.

[5]  D. Oertel,et al.  Inhibitory circuitry in the ventral cochlear nucleus is probably mediated by glycine , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  I. Nelken,et al.  Two separate inhibitory mechanisms shape the responses of dorsal cochlear nucleus type IV units to narrowband and wideband stimuli. , 1994, Journal of neurophysiology.

[7]  Philip H Smith,et al.  Projections of physiologically characterized spherical bushy cell axons from the cochlear nucleus of the cat: Evidence for delay lines to the medial superior olive , 1993, The Journal of comparative neurology.

[8]  Russell R. Pfeiffer,et al.  Classification of response patterns of spike discharges for units in the cochlear nucleus: Tone-burst stimulation , 2004, Experimental Brain Research.

[9]  J. Adams Heavy metal intensification of DAB-based HRP reaction product. , 1981, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[10]  R. Roberts,et al.  GABAergic neurons and axon terminals in the brainstem auditory nuclei of the gerbil , 1987, The Journal of comparative neurology.

[11]  D. Oertel,et al.  Morphology and physiology of cells in slice preparations of the posteroventral cochlear nucleus of mice , 1990, The Journal of comparative neurology.

[12]  R. Wickesberg,et al.  Delayed, frequency-specific inhibition in the cochlear nuclei of mice: a mechanism for monaural echo suppression , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  Eric D. Young,et al.  Response properties of type II and type III units in dorsal cochlear nucleus , 1982, Hearing Research.

[14]  R. Galamboš,et al.  THE RESPONSE OF SINGLE AUDITORY-NERVE FIBERS TO ACOUSTIC STIMULATION , 1943 .

[15]  Marcus Müller,et al.  Structure and function of the cochlea in the African mole rat (Cryptomys hottentotus): evidence for a low frequency acoustic fovea , 1992, Journal of Comparative Physiology A.

[16]  D. Caspary,et al.  A simple technique for constructing 'piggy-back' multibarrel microelectrodes. , 1980, Electroencephalography and clinical neurophysiology.

[17]  M. Sachs,et al.  Classification of unit types in the anteroventral cochlear nucleus: PST histograms and regularity analysis. , 1989, Journal of neurophysiology.

[18]  J. H. Casseday,et al.  Projections from the superior olivary complex to the cochlear nucleus in the tree shrew , 1984, The Journal of comparative neurology.

[19]  Marcus Müller The cochlear place-frequency map of the adult and developing mongolian gerbil , 1996, Hearing Research.

[20]  D. K. Morest,et al.  Relations between auditory nerve endings and cell types in the cat's anteroventral cochlear nucleus seen with the Golgi method and nomarski optics , 1975, The Journal of comparative neurology.

[21]  B. Richmond,et al.  Using response models to estimate channel capacity for neuronal classification of stationary visual stimuli using temporal coding. , 1999, Journal of neurophysiology.

[22]  M. Sachs,et al.  Two-tone inhibition in auditory-nerve fibers. , 1968, The Journal of the Acoustical Society of America.

[23]  R. Rübsamen,et al.  The Medial Nucleus of the Trapezoid Body in the Gerbil Is More Than a Relay: Comparison of Pre- and Postsynaptic Activity , 2003, Journal of the Association for Research in Otolaryngology.

[24]  D. Oertel,et al.  Morphology and physiology of cells in slice preparations of the dorsal cochlear nucleus of mice , 1989, The Journal of comparative neurology.

[25]  C. K. Yuen,et al.  Theory and Application of Digital Signal Processing , 1978, IEEE Transactions on Systems, Man, and Cybernetics.

[26]  D. Ryugo,et al.  Synaptic connections of the auditory nerve in cats: Relationship between endbulbs of held and spherical bushy cells , 1991, The Journal of comparative neurology.

[27]  B. Schofield Superior paraolivary nucleus in the pigmented guinea pig: Separate classes of neurons project to the inferior colliculus and the cochlear nucleus , 1991, The Journal of comparative neurology.

[28]  J. Rothman,et al.  Convergence of auditory nerve fibers onto bushy cells in the ventral cochlear nucleus: implications of a computational model. , 1993, Journal of neurophysiology.

[29]  I. Winter,et al.  Responses of single units in the anteroventral cochlear nucleus of the guinea pig , 1990, Hearing Research.

[30]  W. Warr,et al.  Multiple projections from the ventral nucleus of the trapezoid body in the rat , 1996, Hearing Research.

[31]  M. Abeles,et al.  Multispike train analysis , 1977, Proceedings of the IEEE.

[32]  J. Siegel,et al.  Factors that influence rate-versus-intensity relations in single cochlear nerve fibers of the gerbil. , 1991, The Journal of the Acoustical Society of America.

[33]  J. E. Rose,et al.  Observations on phase-sensitive neurons of anteroventral cochlear nucleus of the cat: nonlinearity of cochlear output. , 1974, Journal of neurophysiology.

[34]  Ian M. Winter,et al.  Diversity of characteristic frequency rate-intensity functions in guinea pig auditory nerve fibres , 1990, Hearing Research.

[35]  Justus Liebig,et al.  Progress in Sensory Physiology , 1981, Progress in Sensory Physiology.

[36]  R. Helfert,et al.  GABA and Glycine Inputs Control Discharge Rate within the Excitatory Response Area of Primary-Like and Phase-Locked AVCN Neurons , 1993 .

[37]  J. Ostwald,et al.  GABA alters the discharge pattern of chopper neurons in the rat ventral cochlear nucleus , 1995, Hearing Research.

[38]  E. Rouiller,et al.  The central projections of intracellularly labeled auditory nerve fibers in cats: an analysis of terminal morphology. , 1986, The Journal of comparative neurology.

[39]  R. Snyder,et al.  Intrinsic connections within and between cochlear nucleus subdivisions in cat , 1988, The Journal of comparative neurology.

[40]  K. Osen,et al.  An atlas of glycine- and GABA-like immunoreactivity and colocalization in the cochlear nuclear complex of the guinea pig , 1992, Anatomy and Embryology.

[41]  R. R. Pfeiffer Anteroventral Cochlear Nucleus:Wave Forms of Extracellularly Recorded Spike Potentials , 1966, Science.

[42]  E D Young,et al.  Excitatory/inhibitory response types in the cochlear nucleus: relationships to discharge patterns and responses to electrical stimulation of the auditory nerve. , 1985, Journal of neurophysiology.

[43]  B. Schofield Projections to the cochlear nuclei from principal cells in the medial nucleus of the trapezoid body in guinea pigs , 1994, The Journal of comparative neurology.

[44]  R. Rübsamen,et al.  Growth of central nervous system auditory and visual nuclei in the postnatal gerbil (Meriones unguiculatus) , 1994, The Journal of comparative neurology.

[45]  K. Ohlemiller,et al.  Functional correlates of characteristic frequency in single cochlear nerve fibers of the Mongolian gerbil , 1990, Journal of Comparative Physiology A.

[46]  D. Irvine The Auditory Brainstem , 1986, Progress in Sensory Physiology.

[47]  R. Zahler Principles of Neurobiological Signal Analysis , 1979, The Yale Journal of Biology and Medicine.

[48]  E. Ostapoff,et al.  A physiological and structural study of neuron types in the cochlear nucleus. II. Neuron types and their structural correlation with response properties , 1994, The Journal of comparative neurology.

[49]  J. Goldberg,et al.  Discharge characteristics of neurons in anteroventral and dorsal cochlear nuclei of cat. , 1973, Brain research.

[50]  J. McGee,et al.  GABA actions within the caudal cochlear nucleus of developing kittens. , 1990, Journal of neurophysiology.

[51]  W. S. Rhode,et al.  Lateral suppression and inhibition in the cochlear nucleus of the cat. , 1994, Journal of neurophysiology.

[52]  Nace L. Golding,et al.  Synaptic inputs to stellate cells in the ventral cochlear nucleus. , 1998, Journal of neurophysiology.

[53]  R. Wickesberg,et al.  Glycinergic Inhibition in the Cochlear Nuclei: Evidence for Tuberculoventral Neurons being Glycinergic , 1993 .

[54]  Donata Oertel,et al.  Tonotopic projection from the dorsal to the anteroventral cochlear nucleus of mice , 1988, The Journal of comparative neurology.

[55]  W. S. Rhode,et al.  Structural and functional properties distinguish two types of multipolar cells in the ventral cochlear nucleus , 1989, The Journal of comparative neurology.

[56]  J. Ostwald,et al.  GABA can improve acoustic contrast in the rat ventral cochlear nucleus , 2004, Experimental Brain Research.

[57]  W. Shofner,et al.  Regularity and latency of units in ventral cochlear nucleus: implications for unit classification and generation of response properties. , 1988, Journal of neurophysiology.

[58]  G. Spirou,et al.  Recordings from cat trapezoid body and HRP labeling of globular bushy cell axons. , 1990, Journal of neurophysiology.

[59]  R. L. Hyson,et al.  Projections from the lateral nucleus of the trapezoid body to the medial superior olivary nucleus in the gerbil , 1992, Hearing Research.