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PubMed1990

Retrograde transport of [3H]glycine from the cochlear nucleus to the superior olive in the guinea pig.

The origins of descending glycinergic projections to the guinea pig cochlear nucleus were investigated using retrograde labelling techniques. To identify the cell groups that provide descending projections to the cochlear nucleus, horseradish peroxidase, a nonspecific retrograde neuronal marker, was injected into the cochlear nucleus. After 24 or 48 hours, labelled cell bodies were evident bilaterally in all of the periolivary nuclei that surround the lateral and medial superior olive. The largest numbers of labelled neurons were located in the ventral nucleus of the trapezoid body bilaterally and in the lateral nucleus of the trapezoid body and dorsal periolivary nucleus ipsilaterally. Labelled cells were also present in the inferior colliculus bilaterally and in the contralateral cochlear nucleus. [3H]Glycine was employed as a retrograde tracer to identify the cell groups providing descending glycinergic projections to the cochlear nucleus. Three to 48 hours after injection of 19, 190, or 380 microM [3H]glycine into the cochlear nucleus, retrogradely labelled cell bodies were observed ipsilaterally in all of the periolivary nuclei. No labelled neurons were found in the inferior colliculus. After injections of the highest concentration of [3H]glycine, labelled cells were also found contralaterally in the ventral and lateral nuclei of the trapezoid body and also in the contralateral cochlear nucleus. We conclude that descending glycinergic projections to the cochlear nucleus originate mostly in ipsilateral periolivary cell groups. Minor glycinergic projections originate from the contralateral cochlear nucleus and also from the contralateral ventral and lateral nuclei of the trapezoid body.

Animals↗

PubMed1989

Place-pitch and vowel-pitch comparisons in cochlear implant patients using the Melbourne-Nucleus cochlear implant.

Results of place-pitch and vowel-pitch comparisons are presented in 21 cochlear implant patients using the Melbourne-Nucleus cochlear implant. Vowel-pitch comparisons were also carried out in 10 normal hearing subjects. A technique for the place-pitch ranking test has been developed. A graphic representation of the results shows the well-ranked electrodes in sequential pitch-order, and reveals any indication of abnormal place-pitch perception. It aids the selection of correctly place-pitch ranked electrodes. The vowel-pitch comparisons showed that both normal hearing subjects and cochlear implant patients are able to rank vowels according to 'vowel-pitch'. In normal hearing subjects, three main types of vowel-pitch processing have been found. Results indicate that an information selection and reduction process occurs at higher levels along the auditory pathway. Cochlear implant patients test results showed the limited contribution of the first and the virtual lack of the second formant's contribution to pitch-ranking the voiced vowels. These results indicate that fundamental frequency converted to pulse rate may not be adequate at certain segments along the cochlear partition. Vowels are not perceived by cochlear implant patients according to their first or second formant frequency converted to place-pitch. There would seem to be a need for alternative speech processing strategies in the Melbourne-Nucleus implant.

Adult↗

PubMed1985

The use of intracellular techniques in the study of the cochlear nucleus.

This paper describes part of the anatomy and physiology of the cochlear nucleus and some of the recent techniques developed to study the structure and function of the cochlear nucleus. The cochlear nucleus is the first region in the brain stem that receives information from the auditory nerve. The use of intracellular markers has made possible a new detail of description that should increase significantly our understanding of how the cochlear nucleus organizes the neural information transmitted to it from the auditory nerve.

Animals↗

PubMed1997

Simultaneous anterograde labeling of axonal layers from lateral superior olive and dorsal cochlear nucleus in the inferior colliculus of cat.

The laminar organization of the central nucleus of inferior colliculus includes layers of axons that may be important in shaping the responses of neurons. Depending on their source, some layered axons are afferents that are superimposed and terminate on the same postsynaptic neurons, while other layered afferents, such as those from the ipsilateral and contralateral lateral superior olive, terminate side-by-side. The specific pattern of convergence may dictate which populations of axons are presynaptic to layered disc-shaped neurons in the central nucleus. We compared the distribution of afferent axons from the dorsal cochlear nucleus and the lateral superior olive to the contralateral inferior colliculus in the cat. Injection sites in cochlear nucleus and superior olive were physiologically characterized by extracellular recordings of single and multiple units in response to monaural and binaural acoustic stimulation. Two separate injections were made in each case, and both injection sites contained units with overlapping best frequencies. Biotinylated dextran, fluorescent dextran, 3H-leucine, and wheat germ agglutinin conjugated to horseradish peroxidase were used as anterograde tracers. The present results show that layered axons from the dorsal cochlear nucleus and lateral superior olive are superimposed in part of the contralateral central nucleus. Both projections were arranged in rostro-caudally oriented axonal layers that converged in the ventral part of the central nucleus. However, in the dorsal part of the central nucleus, the same layer of axons from the dorsal cochlear nucleus did not terminate with afferents from the lateral superior olive. Within the overlapping layers in the ventral central nucleus, the overlap of axons from the dorsal cochlear nucleus and the lateral superior olive was uniform except for small patches that were usually smaller than the dendritic fields of disc-shaped neurons. These data suggest that the layers may create specific functional zones in the central nucleus of the inferior colliculus. One zone may contain neurons with binaural responses that combine the properties of the inputs from the contralateral lateral superior olive and the dorsal cochlear nucleus. A second zone may contain inputs from the cochlear nucleus but lack those of the lateral superior olive.

Afferent Pathways↗

PubMed2002

Computational diversity in the cochlear nucleus angularis of the barn owl.

The cochlear nucleus angularis (NA) is widely assumed to form the starting point of a brain stem pathway for processing sound intensity in birds. Details of its function are unclear, however, and its evolutionary origin and relationship to the mammalian cochlear-nucleus complex are obscure. We have carried out extracellular single-unit recordings in the NA of ketamine-anesthetized barn owls. The aim was to re-evaluate the extent of heterogeneity in NA physiology because recent studies of cellular morphology had established several distinct types. Extensive characterization, using tuning curves, phase locking, peristimulus time histograms and rate-level functions for pure tones and noise, revealed five major response types. The most common one was a primary-like pattern that was distinguished from auditory-nerve fibers by showing lower vector strengths of phase locking and/or lower spontaneous rates. Two types of chopper responses were found (chopper-transient and a rare chopper-sustained), as well as onset units. Finally, we routinely encountered a complex response type with a pronounced inhibitory component, similar to the mammalian typeIV. Evidence is presented that this range of response types is representative for birds and that earlier conflicting reports may be due to methodological differences. All five response types defined were similar to well-known types in the mammalian cochlear nucleus. This suggests convergent evolution of neurons specialized for encoding different behaviorally relevant features of the auditory stimulus. It remains to be investigated whether the different response types correlate with morphological types and whether they establish different processing streams in the auditory brain stem of birds.

Acoustic Stimulation↗

PubMed1996

Dorsal cochlear nucleus blood flow during acoustic stimulation.

Dynamic in vivo changes in dorsal cochlear nucleus blood flow during pure-tone stimulation were assessed with intravital microscopy. Subjects were stimulated with 5-, 10-, or 15-kHz pure tones at 70, 80, and 90 dB sound pressure level. Measurements in red blood cell velocity and vessel diameter were made in capillaries overlying the 10-kHz isofrequency band of the dorsal cochlear nucleus. Stimulation with 10 kHz induced intensity-dependent increases in local blood flow in the 10-kHz isofrequency band of the dorsal cochlear nucleus. Stimulation with 5 kHz and 15 kHz, frequencies represented in remote locations on the dorsal cochlear nucleus surface, did not significantly alter blood flow in the defined 10-kHz isofrequency band. These data demonstrate a direct relationship between spectral and intensity-dependent pure-tone stimulation of the dorsal cochlear nucleus and increases in local blood flow. These findings suggest that tonal stimulation of the dorsal cochlear nucleus induces an increase in local metabolic demands with resultant rapid blood flow increases.

Acoustic Stimulation↗

PubMed2005

Auditory cortical projections to the cochlear nucleus in guinea pigs.

We used anterograde tracing techniques to examine projections from auditory cortex to the cochlear nucleus in guinea pigs. Following injection of dextrans into the temporal cortex, labeled axons were present bilaterally in the cochlear nucleus. The distribution of boutons within the cochlear nucleus was similar on the two sides. The majority of boutons was usually located on the ipsilateral side. Most of the boutons were located in the granule cell areas, where many small boutons and a few larger, mossy-type endings were labeled. Additional small, labeled boutons were found in all layers of the dorsal cochlear nucleus, with the majority located in the fusiform cell layer. Labeled boutons were also present in the ventral cochlear nucleus, where they were located in the small cell cap as well as magnocellular parts of both posteroventral and anteroventral cochlear nucleus. Similar results were obtained with injections restricted to primary auditory cortex or to the dorsocaudal auditory field. The results illustrate direct cortical projections to the cochlear nucleus that are likely to modulate the activity in a number of ascending auditory pathways.

Animals↗

PubMed1997

Modeling inhibition of type II units in the dorsal cochlear nucleus.

Type II units in the dorsal cochlear nucleus (DCN) are characterized by vigorous but nonmonotonic responses to best frequency tones as a function of sound pressure level, and relatively weak responses to noise. A model of DCN neural circuitry was used to explore two hypothetical mechanisms by which neurons may be endowed with type II unit response properties. Both mechanisms assume that type II units receive excitatory input from auditory nerve (AN) fibers and inhibitory input from an unspecified class of cochlear nucleus interneurons that also receive excitatory AN input. The first mechanism, a lateral inhibition (LI) model, supposes that type II units receive inhibitory input from a number of narrowly tuned interneurons whose best frequencies (BFs) flank the BF of the type II unit. Tonal stimuli near BF result in only weak inhibitory input, but broadband stimuli recruit enough lateral inhibitors to greatly weaken the type II unit response. The second mechanism, a wideband inhibition (WBI) model, supposes that type II units receive inhibitory input from interneurons that are broadly tuned so that they respond more vigorously to broadband stimuli than to tones. Physiological and anatomical evidence points to the possible existence of such a class of neurons in the cochlear nucleus. The model extends an earlier computer model of an iso-frequency DCN patch to multiple frequency slices and adds a population of interneurons to provide the inhibition to model type II units (called 12-cells). The results show that both mechanisms accurately simulate responses of type II units to tones and noise. An experimental paradigm for distinguishing the two mechanisms is proposed.

Acoustic Stimulation↗

PubMed1997

[A quantitative study on the cells of cochlear nucleus in rats at different ages].

The volume of cochlear nucleus and nucleolus, neural populations were determined in rats of three groups aged (1, 2-3, 22-28 months). The study data indicated that there is no difference between the volume of cochlear nucleus in the aged and adult animals (P > 0.05). Compared with the other two groups, the aged animals show a reduction of volume of necleolus of cochlear nucleus neurons (P < 0.01), a loss of neurons (spherical cell and multipolar cell) (P < 0.01). On the other hand, it shows an increase in number for the glial cells in the aged animals (48.48%, P < 0.01). Quantitative results of the cell of cochlear nucleus were analysed. We suggest that central changes also play an important role in presbycusis.

Age Factors↗

PubMed1986

Immunocytochemical localization of GABA in the cochlear nucleus of the guinea pig.

The immunocytochemical distribution of gamma-aminobutyric acid (GABA) was determined in the cochlear nucleus of the guinea pig using affinity-purified antibodies made against GABA conjugated to bovine serum albumin. Light microscopic immunocytochemistry shows immunoreactive puncta, which appear to be GABA-positive presynaptic terminals, distributed throughout the cochlear nucleus. In the ventral cochlear nucleus, these puncta are often found around unlabeled neuronal cell bodies. While occasional labeled small cells are found in the ventral cochlear nucleus, most GABA-immunoreactive cell bodies are present in the superficial layers of the dorsal cochlear nucleus. Based on size and shape, immunoreactive cells in the dorsal cochlear nucleus are divided into 3 classes: medium round cells with diameters averaging 16 microns, small round cells with average diameters of 9 microns and small flattened cells with major and minor diameters averaging 11 and 6 microns, respectively. Labeled fusiform and granule cells are not seen. A similar distribution of label was seen using antibodies against glutamic acid decarboxylase. Electron microscopic immunocytochemistry of the anteroventral cochlear nucleus shows GABA immunoreactive boutons containing oval/pleomorphic synaptic vesicles on cell bodies and dendrites. Other major classes of terminals, including those with small round, large round and flattened synaptic vesicles are unlabeled.

Animals↗

PubMed2001

Connections between the dorsal raphe nucleus and a hindbrain region consisting of the cochlear nucleus and neighboring structures.

Previous studies have shown that neurons in the raphe nuclei respond to acoustic stimuli. The present study investigated connections between the dorsal raphe nucleus (DRN) and a hindbrain region consisting of the cochlear nucleus (CN) and neighboring structures. A mixture of one or more tracers (cholera toxin B, biotinylated dextran amine (BDA), and 3H-leucine) was injected into the cat DRN. Retrograde-labeling results are presented whereby a new structure, to be called the juxta-acoustico-floccular fascicle (JAFF), is identified. The JAFF is surrounded by the CN, flocculus, lateral cerebellar nucleus, lateral vestibular nucleus, and restiform body. The JAFF is closely associated with the infracerebellar nucleus (ICN). Labeled neurons projecting to the DRN were concentrated in the JAFF, embedded among axons. Less numerous labeled neurons were in the ICN and CN. Anterograde-labeling results are presented showing fibers labeled with BDA or with BDA and 3H-leucine in the CN, cochlear nerve and vestibular nerve, indicating that the DRN projects to these structures. The ascending and descending connections between the DRN and the above hindbrain region may mediate a reflex that may alter the sensitivity of the auditory system in response to biologically salient (e.g. threatening or attractive) stimuli.

Animals↗

PubMed1995

Development of ventral cochlear nucleus projections to the superior olivary complex in gerbil.

The postnatal development of the projection from the ventral cochlear nucleus to the principal nuclei in the superior olivary complex in gerbil (Meriones unguiculatus) was studied in an age-graded series of pups ranging from 0 to 18 days old. Small crystals of 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiI) were inserted into the ventral cochlear nucleus of aldehyde-fixed brains, and the labeled projections were examined with epifluorescence microscopy. Selected sections were photooxidized in a solution of diaminobenzidine and subsequently processed for electron microscopy to examine the development of labeled synapses in the target nuclei. Horseradish peroxidase was injected into the ventral cochlear nucleus of adult gerbils to assess the form and persistence of projections observed in the neonatal animals. In addition, electrophysiological responses to acoustic stimuli of single units in the adult auditory brainstem were analyzed to confirm the functionality of the novel projection from the ventral cochlear nucleus to the contralateral lateral superior olive. By the day of birth (P0), developing axons from the ventral cochlear nucleus have already established highly ordered pathways to the three primary nuclei of the superior olivary complex: the ipsilateral lateral superior olive, the contralateral medial nucleus of the trapezoid body, and at the lateral and medial dendrites of the ipsilateral and contralateral medial superior olive, respectively. Developing axons from the ventral cochlear nucleus that innervated the contralateral medial nucleus of the trapezoid body lacked the terminal morphology characteristic of the calyx of Held, but began to adopt a more characteristic form on P5. The mature calyx appeared around P14-16. Exuberant developmental projections to topographically inappropriate areas of the superior olivary complex were not observed at the postnatal ages studied. In addition to the projections of the ventral cochlear nucleus to the superior olivary complex described in other species, we observed the development and maintenance of a major direct projection from the ventral cochlear nucleus to the contralateral lateral superior olive. On P0, ventral cochlear nucleus axons decussate in the dorsal trapezoid body, form a plexus at the dorsal edge of the contralateral medial superior olive, and enter the ventrolateral limb of the contralateral lateral superior olive. Over the next 2 weeks, fascicles of fibers form on the hilar and ventral aspects of the ventrolateral limb. Fibers arising from these fascicles form converging, but nonoverlapping, arborizations within the ventrolateral limb at right angles to the curvature of the nucleus. The medial region was devoid of labeled axons.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1984

Intracellular marking of physiologically characterized cells in the ventral cochlear nucleus of the cat.

In the cat ventral cochlear nucleus, separate neuronal classes have been defined based on morphological characteristics; physiologically defined unit types have also been described based on the shape of post-stimulus-time-histograms in response to tone bursts at characteristic frequency. The aim of the present study was to address directly the issue of how morphological cell types relate to physiological unit types. We used intracellular injections of horseradish peroxidase to stain individual neurons after their response characteristics were determined by intracellular recordings. The maintenance of a continuous negative resting potential, the correspondence of the calculated position of the electrode tip at the time of injection to the location of the stained neuron, and the similarity of response properties collected before and after the injection provide evidence that the injected, stained, and recovered neuron corresponds to the functionally defined unit. In the region around the nerve root in the anteroventral cochlear nucleus, two " primarylike " and one " primarylike with notch" units were "bushy" cells. "Bushy" cells are characterized by primary dendrites arising from one hemisphere of the soma and ramifying repeatedly to produce their bushy dendritic arbor. In this same region, the "chopper" and two "on" units were also "bushy" cells. In the posteroventral cochlear nucleus, the "chopper" unit was a "stellate" cell and the "on" unit was an "octopus" cell. These results are partially consistent with previous conclusions based on correlations established between the regional distribution of physiological unit types and morphological cell types. More importantly, they confirm and extend recent intracellular marking data (Rhode et al., ' 83b ). If our classification schemes have functional significance, we are left with the conclusion that the distinction between "bushy" and "stellate" cells in the auditory nerve root region of the ventral cochlear nucleus does not correspond in any simple way to distinctions between physiological unit types. More than one morphological cell type can exhibit the same particular response patter, and the same morphological cell type can exhibit several different response patterns.

Animals↗

PubMed1994

Exposure to low frequency noise during rearing induces spongiform lesions in gerbil cochlear nucleus: high frequency exposure does not.

Spongiform lesions of the gerbil cochlear nucleus are reduced in number and extent by rearing in acoustic isolation compared with rearing while exposed to normal colony low-frequency background noise. This study tested whether rearing under exposure to noise bands of moderate intensity would increase the number and extent of cochlear nucleus spongiform lesions. Gerbils were reared from weaning to young adulthood in acoustic isolation chambers while continually exposed to moderately intense bands of either high frequency or low frequency noise. Exposure to low frequency noise resulted in lesion number and area densities that were more than twice those seen in gerbils exposed to high frequency noise. Lesion extent in the low frequency group was similar to that in colony-reared gerbils; lesion extent in the high frequency group was similar to gerbils reared in acoustic isolation. Comparisons within the posterior ventral cochlear nucleus revealed that the differences in lesion extent were most pronounced in the middle and dorsal-medial portions, the regions that are most responsive to middle and high frequencies. These finding suggest that the regional restriction of spongiform lesions within the cochlear nucleus does not have a tonotopic basis.

Acoustic Stimulation↗

PubMed2004

Mossy fibers in granule cell areas of the rat dorsal cochlear nucleus from intrinsic and extrinsic origin innervate unipolar brush cell glomeruli.

Non tonotopic transmission between cochlear nuclei and other auditory and non-auditory nuclei in the brain is probably due to large axonal terminals (mossy fibers) innervating granule cell areas of cochlear nuclei. The origin of mossy fibers in the dorsal cochlear nucleus (DCN) is multiple, from other auditory or non-auditory nuclei but possibly also from intrinsic neurons. The present ultrastructural immunocytochemical study reports for the first time the presence of anterograde-labeled mossy fibers in the DCN of the rat after injection of the neural tracer WGA-HRP into 3 different nuclei. Labeled mossy fibers were seen in 9.0% of mossy fibers detected after tracer injection into the ipsilateral anteroventral cochlear nucleus, in 7.3% of mossy fibers after contralateral collicular injection, and 13.2% after contralateral cochlear nucleus injection. Most (over 95%) mossy fibers contained round vesicles, both large and small, and were likely excitatory terminals, but few showed flat-pleomorphic vesicles that contained the inhibitory neurotransmitters GABA and glycine. Most of the anterograde-labeled ipsilateral mossy fibers containing small round synaptic vesicles, are probably derived from multipolar neurons within the ipsilateral anteroventral cochlear nucleus. After injections into the contralateral inferior colliculus, it was not possible to distinguish putative descending collicular mossy fibers from intrinsic mossy fibers. The latter would suggest the presence of an amplification pathway within the DCN, from collateral axons of pyramidal or stellate cells of the ipsilateral ventral cochlear nucleus to form glomeruli with granule-unipolar brush cells. After injection into the contralateral cochlear nucleus, it was not possible to distinguish between commissural mossy fibers and those derived from ipsilateral recurrent axon-terminals of commissural neurons within the DCN or the ventral cochlear nucleus. Despite this limitation, the present observations show that extrinsic or intrinsic mossy fibers reach granule cell areas in layers 2 and 3 of the DCN and form glomeruli of large or small dimension (1.5-4 microm) with unipolar brush and granule cells. These mossy fibers probably carry a fast excitatory non-tonotopic input which may influence the electrical response of granule cell areas.

Animals↗

PubMed1982

Descending projections from the inferior colliculus to the dorsal cochlear nucleus in the cat: an autoradiographic study.

Descending auditory projections from different subdivisions of the inferior colliculus to the dorsal cochlear nucleus were investigated in experiments using the autoradiographic technique. Tritiated leucine injections confined to the pericentral nucleus of the inferior colliculus resulted in the appearance of dense grain clusters distributed over the outer fusiform cell and molecular layers of the ipsilateral dorsal cochlear nucleus. The pattern and distribution of dense grain clusters strongly resembled the central terminals of glomeruli described previously in the dorsal cochlear nucleus. Injections into the dorsal region of the central nucleus of the inferior colliculus led to a more diffuse distribution of grains over the middle and outer fusiform cell layer and over the innermost molecular layer of the dorsal cochlear nucleus on both sides. Dense grain clusters were also evident after these injections but they appeared to result from the concomitant injection into the overlying pericentral nucleus. Finally, injections of tritiated leucine into the ventral region of the central nucleus of the inferior colliculus (which included some cells of the dorsal nucleus of the lateral lemnisus) resulted in the heaviest labelling of the dorsal cochlear nucleus. Grains were distributed perisomatically and peridendritically around fusiform cells of the fusiform cell layer and giant cells of the deep dorsal cochlear nucleus on both sides. The results indicate that the pericentral nucleus and the more dorsal region of the central nucleus of the inferior colliculus establish overlapping connections with the outermost fusiform cell and molecular layers of the dorsal cochlear nucleus. Both sets of connections seem to be made principally with interneurons through glomerular and other inputs to scattered small cells which exist in these laminae. Since cortical and thalamic descending fibers directly innervate only the most dorsal regions of the inferior colliculus, it may be that this region of the tectum selectively mediates activity from these higher auditory centers. Such centers may indirectly influence fusiform cell response properties through collicular inputs to small cells of the dorsal cochlear nucleus that contact fusiform cells. A more substantial and direct projection was shown to arise from the ventral region of the inferior colliculus to innervate both the fusiform and giant cells. As such, the descending connections from the ventral inferior colliculus may be more likely to influence directly the output of both the fusiform and giant cells and, therefore, the projection of auditory information from the dorsal cochlear nucleus to higher levels.

Animals↗

PubMed1998

Postnatal development of GABA- and glycine-like immunoreactivity in the cochlear nucleus of the Mongolian gerbil (Meriones unguiculatus).

The maturation of the morphological substrate for inhibitory interactions was investigated in the cochlear nucleus of the gerbil with immunocytochemistry for gamma aminobutyric acid (GABA) and glycine on alternating vibratome sections. The patterns of immunostaining obtained with both antibodies in the adult closely conformed to the general mammalian scheme. Qualitative analyses revealed an age-related increase in staining intensity and in the relative numbers of immunolabelled cells after birth up to the age of 3-4 weeks. As early as birth and in all subdivisions of the cochlear nucleus, a few labelled cells and puncta in the sections were stained either with the GABA or the glycine antibody. Immunoreactive puncta and cells were, however, far less abundant than in the adult, and the staining intensity of cells was only weak. The most strikingly GABA-immunolabelled cells at birth were the Golgi cells of the granule-cell domains. The numbers of weakly GABA- and glycine-immunostained cells of the dorsal cochlear nucleus clearly increased between birth and the third postnatal week. At approximately the onset of hearing (postnatal day 12-14), some cells of the dorsal cochlear nucleus and small cells of the ventral cochlear nucleus gained adult-like GABA-staining properties. Almost adult-like labelling intensity was observed in glycine-immunoreactive cells of the deep dorsal cochlear nucleus and in some small cells of the ventral cochlear nucleus. Puncta staining to both antibodies appeared adult-like throughout the cochlear nucleus. About 2 weeks after the onset of hearing (at the latest), adult-like staining of all subsets of immunoreactive cells occurred throughout the cochlear nucleus in all specimens.

Animals↗

PubMed1991

[Response of the cochlear nucleus neurons of the cat to tone-burst-trains].

Although both posteroventral cochlear nucleus (PVCN) and dorsal cochlear nucleus (DCN) are innervated by the descending branch of auditory nerve fibers, their intrinsic morphological organizations are so different that their physiological roles are expected to be different in signal processing. Temporal information coding of acoustic signals in the cochlear nucleus was examined by using stimuli of "tone-burst-trains (TBT)". Responses of cochlear nucleus neurons of anesthetized cats were recorded either intracellularly or extracellularly. Responses of the neurons to TBT stimuli were classified into "adaptive type" and "non-adaptive type". The "adaptive type" neurons were mainly recorded from PVCN. Responses of these neurons to TBT stimuli decayed exponentially, because of short-term adaptation, in the subsequent tone-bursts. These neurons faithfully preserve the adaptative behavior of auditory nerve fibers. On the contrary, the "non-adaptive type" neurons were mainly found in DCN. They showed variety of responses to TBT stimuli including facilitation, disinhibition and inhibition depending on duration and/or interval of tone-bursts. Our results suggest that some "non-adaptive type" neurons, showing facilitative and/or inhibitory responses to TBT stimuli, act as temporal filters that extract temporal information from acoustic signals.

Acoustic Stimulation↗