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PubMed1992

Mapping of c-fos expression elicited by pure tones stimulation in the auditory pathways of the rat, with emphasis on the cochlear nucleus.

C-fos expression was mapped in the auditory pathways of rats, stimulated acoustically with pure tones. In the cochlear nucleus, two clusters of c-fos-like immunoreactive neurons, located respectively in the caudal part of the dorsal cochlear nucleus and in the granular cell region, did not show clear systematic shift in their position as a function of the tones frequency. On the other hand, more rostrally in the dorsal cochlear nucleus, a cluster of c-fos-like positive neurons moved progressively from dorsal to ventral for decreasing tones frequency. In the posteroventral cochlear nucleus, another cluster of c-fos-like positive neurons was observed, whose position also varied with tones frequency. Surprisingly, no or very rare c-fos-like immunoreactive neurons were present in the anteroventral cochlear nucleus and in the superior olivary complex. In the inferior colliculus, however, c-fos-like immunoreactive neurons formed clear isofrequency contours, shifting from dorsolateral to ventromedial for increasing tones frequency. In the medial geniculate body c-fos-like immunostaining was restricted to the medial and dorsal divisions while the ventral division was free of labeling. The cause of this differential labeling along the auditory pathways is at present unknown but may eventually provide clues as to physiological differences in parallel auditory pathways.

Acoustic Stimulation↗
PubMed1998

Directed outgrowth from a subset of cochlear nucleus fibers in a collagen-gel matrix

We have employed a collagen-gel co-culture system to evaluate the influence of the hindbrain floor-plate on initial axon outgrowth from the cochlear nucleus. After 2 days in vitro, cochlear nucleus explants exhibited directed outgrowth towards co-cultured floor-plate explants. Comparisons with co-cultures of cochlear nucleus/forebrain or cochlear nucleus/midbrain explants or with cochlear nucleus explants cultured alone suggest that the floor-plate has a specific chemoattractant effect on the outgrowth of the pioneer fibers of the hindbrain auditory commissure. Fiber outgrowth was not directed towards a recombinant source of the chemoattractant molecule netrin suggesting that floor-plate-directed outgrowth in the cochlear nucleus is not solely dependent on netrin. In the present report, we present evidence for the first time that the floor-plate is a chemotropic source in pathfinding of second-order auditory fibers from the cochlear nucleus in the hindbrain.

Journal Article↗
PubMed1987

Effects of trapezoid body and superior olive lesions on choline acetyltransferase activity in the rat cochlear nucleus.

Using a microdissection and quantitative microassay approach, choline acetyltransferase activities were mapped in the cochlear nuclei of rats having either transection of the trapezoid body or destruction of the superior olivary complex on one side in the brain stem. Lateral trapezoid body transection resulted in dramatic loss of choline acetyltransferase activity in all parts of the ipsilateral cochlear nucleus, while more medial transection had little effect. Destruction of the superior olivary complex resulted in dramatic loss of choline acetyltransferase activity in the ipsilateral cochlear nucleus, and detectable loss also contralaterally. The results suggest that most of the centrifugal cholinergic projections to the rat cochlear nucleus derive from or traverse the vicinity of the superior olivary complex bilaterally and enter the cochlear nucleus ventrally from the region of the trapezoid body.

Animals↗
PubMed2003

Ultrastructure and immunocytochemical characteristics of cells in the octopus cell area of the rat cochlear nucleus: comparison with multipolar cells.

Cells in the octopus cell area of the rat ventral cochlear nucleus have been connected to the monaural interpretation of spectral patterns of sound such as those derived from speech. This is possible by their fast onset of firing after each octopus cell and its dendrites have been contacted by many auditory fibres carrying different frequencies. The cytological characteristics that make these large cells able to perform such a function have been studied with ultrastructural immunocytochemistry for glycine, GABA and glutamate, and compared to that of other multipolar neurons of other regions of the ventral cochlear nucleus. Cells in the octopus cell area have an ultrastructure similar to large-giant D-multipolar neurons present in other areas of the cochlear nucleus, from which they differ by the presence of a larger excitatory axo-somatic synaptic input and larger mitochondria. Octopus cells are glycine and GABA negative, and glutamate positive with different degree. Large octopus cells receive more axo-somatic boutons than smaller octopus cells. Fusiform octopus cells are found sparsely within the intermediate acoustic striae. These cells are large to giant excitatory neurons (23-35 microm) with 62-85% of their irregular perimeter covered with large axo-somatic synaptic boutons. Most boutons contain round vesicles and are glycine and GABA negative but glutamate positive. The latter excitatory boutons represent about 70% of the input to octopus cells. Glycine positive boutons with flat and pleomorphic vesicles account for 9-10% of the input while GABA-ergic boutons with pleomorphic vesicles represent about 20% of the synaptic input. Other few, multipolar cells within the rat octopus cell area are surrounded by more inhibitory than excitatory terminals which contain flat and pleomorphic vesicles, a feature distinctive from that of true octopus cells. The latter resemble multipolar cells seen outside the octopus cell area that project to the contralateral inferior colliculus and cochlear nucleus. Based on this study, two types of large multipolar cells are present in the octopus cell area: 1) those that receive about 70% of axo-somatic R boutons and stain more intensely for glutamate may correspond to pure onset neurons (Oi); 2) those with less than 33% of R axosomatic boutons, with less immunoreactivity to glutamate and sometimes glycine positive may represent the onset chopper neurons (Oc). In the octopus cell area the first type appears more prevalent. The present study suggests that octopus cells are a special type of excitatory D-multipolar neuron confined to the octopus cell area and mainly innervated by glutamatergic cochlear nerve terminals.

Animals↗
PubMed1983

Auditory evoked potentials recorded from the cochlear nucleus and its vicinity in man.

Intracranial responses from the auditory nerve and the cochlear nucleus were recorded from patients undergoing neurosurgical operations during which these structures were exposed. Responses to stimulation of the ipsilateral ear with short tonebursts from the vicinity of the cochlear nucleus show a large surface-negative peak, the latency of which is close to that of peak III in the auditory brain-stem evoked potentials recorded from scalp electrodes. There was also a response to contralateral stimulation, smaller in amplitude and with a longer latency. It is concluded that the cochlear nucleus is the main generator of peak III responses, and that structures of the ascending auditory pathway that are more central than the cochlear nucleus are unlikely to contribute to wave III of the auditory brain-stem evoked potentials.

Brain Stem↗
PubMed2002

Ascending and descending projections from the superior olivary complex in guinea pigs: different cells project to the cochlear nucleus and the inferior colliculus.

The superior olivary complex is a source of ascending projections to the inferior colliculus and descending projections to the cochlear nucleus. We used multiple-labeling techniques with fluorescent retrograde tracers to determine whether individual superior olivary cells project to the inferior colliculus and the cochlear nucleus. Almost all labeled cells contained one tracer, suggesting that they projected to only one of the injected targets. A small number of cells sent collateral projections to the ipsilateral cochlear nucleus and ipsilateral inferior colliculus. The double-labeled cells constituted fewer than 2% of the cells that projected to the cochlear nucleus or to the inferior colliculus. There was no evidence for cells projecting to both contralateral targets or to one ipsilateral target and one contralateral target. We conclude that the ascending projections to the inferior colliculus and the descending projections to the cochlear nucleus arise almost exclusively from separate populations of cells in the superior olivary complex. Their separate origins suggest that these projections are sending different information to higher and lower centers of the auditory pathways.

Animals↗
PubMed1999

Reduced spontaneous activity in the dorsal cochlear nucleus of Scn8a mutant mice.

Spontaneous activity was recorded in the dorsal cochlear nucleus of brain slices from mice homozygous for the med-J and jolting mutations in the neuronal sodium channel alpha-subunit Scn8a. Densities of spontaneously active neurons in slices from both mutants were significantly lower than in control slices. Spontaneous firing patterns with bursts of action potentials were recorded from approximately 50% of the neurons in control slices, but the typical bursting patterns were not observed in neurons of med-J and jolting mouse slices. The results suggest that this voltage-gated sodium channel is essential for the spontaneous bursting firing of cochlear nucleus cartwheel neurons. This mutant animal model may be useful for the study of the functional roles of cochlear nucleus neurons.

Action Potentials↗
PubMed1982

Anatomy and physiology of the gerbil cochlear nucleus: an improved surgical approach for microelectrode studies.

A new, improved surgical approach to the cochlear nucleus is developed in the gerbil. This new approach involves making a small hole in the lateral wall of the temporal bone located within the perimeter of the superior semicircular canal. Microelectrodes are passed through the intact parafloccular lobe of the cerebellum to the cochlear nucleus. One advantage of the new approach is that no removal of any CNS vasculature or neural tissue is necessary. Relations between the bulla, temporal bone and cochlear nucleus are presented in detail. The new approach is demonstrated by making single unit recordings from the cochlear nucleus and classifying response patterns as measured in PST histograms. All of the response types found in cat are found in the gerbil.

Animals↗
PubMed2004

Organization of inhibitory feed-forward synapses from the dorsal to the ventral cochlear nucleus in the cat: a quantitative analysis of endings by vesicle morphology.

The main ascending, excitatory pathway from the cochlea undergoes synaptic interruption in the dorsal and ventral cochlear nuclei. The dorsal cochlear nucleus also forms a feed-forward circuit, which receives cochlear input and projects to the ventral cochlear nucleus by a tuberculo-ventral tract. This circuit may provide an inhibitory fringe (side bands) surrounding the center bands of the main ascending pathway. Biotinylated dextran injections into the dorsal cochlear nucleus anterogradely labeled the tuberculo-ventral tract and its endings in the anteroventral cochlear nucleus but also retrogradely filled cochlear nerve fibers and their terminals in the same regions. To distinguish tuberculo-ventral from cochlear nerve terminals, we used electron microscopy of the immunolabeled endings. Images were digitized and filter-enhanced, and the sizes and shapes of synaptic vesicles were used to construct quantitative profiles of the terminal types. The cochlear nerve endbulbs mapped to the same iso-frequency band of the injection site (main band). Flanking the main band were smaller labeled endings. About 45% of labeled terminals were pleomorphic and equally represented in the main band and side bands. Therefore, if there is an inhibitory fringe in the main projection pathway, it was not selective for tuberculo-ventral tract endings. Surprisingly, an excitatory category of round vesicles of intermediate size was labeled in the main band but not in the side bands. These intermediate endings may balance the feed-forward inhibition from the tuberculo-ventral tract. The quantitative method devised for classification of ending types by their vesicle profiles should be a generally useful tool for analysis.

Animals↗
PubMed2000

Projection of the marginal shell of the anteroventral cochlear nucleus to olivocochlear neurons in the cat.

The marginal shell of the anteroventral cochlear nucleus is anatomically and physiologically different from its central core. Previous studies suggest that neurons in the marginal shell are well suited to encode the intensity of acoustic stimuli. To investigate the projections of the marginal shell, a focal injection (<100 nl) of a mixture of biotinylated dextran amine (BDA) and (3)H-leucine was made into the marginal shell of the cat combined with injection of cholera toxin subunit-B (CTB) into the cochleas. Following a 7-day survival, the cats were perfused. Axons and swellings labeled with BDA and olivocochlear neurons labeled with CTB were immunocytochemically stained black and brown, respectively. (3)H-leucine labels were visualized by autoradiography. Labeled neural structures were examined via light microscopy. We found that swellings labeled with BDA, sometimes doubly labeled with BDA and (3)H-leucine, were in close apposition with dendrites and/or somata of olivocochlear neurons identified with CTB labeling. Double labeling with BDA and (3)H-leucine signifies that the label was anterogradely transported. The results support the conclusion that the anteroventral cochlear nucleus projects to medial olivocochlear neurons bilaterally and to lateral olivocochlear neurons ipsilaterally. Furthermore, the results are consistent with the interpretation that the marginal shell provides a source of the above-mentioned projections. Together with information in the literature, the present anatomical results support a hypothesis that the marginal shell provides information about stimulus intensity as a part of a reflex (or feedback gain control) system comprising the cochlea, cochlear neurons, cochlear nucleus, medial olivocochlear neurons, and cochlear outer hair cells.

Animals↗
PubMed1992

Transneuronal labeling of cochlear nucleus neurons by HRP-labeled auditory nerve fibers and olivocochlear branches in mice.

Auditory nerve fibers were labeled by extracellular injections of horseradish peroxidase into the spiral ganglion in mice. The labeled fibers were traced in an anterograde direction through the auditory nerve into the cochlear nucleus. In almost half of the injections, the labeled endings of auditory nerve fibers contacted cochlear nucleus neurons that were also labeled with horseradish peroxidase and were presumably transneuronally labeled. Only darkly labeled endings were associated with transneuronally labeled neurons, but not all darkly labeled endings had targets that were transneuronally labeled. Transneuronal labeling occurred almost exclusively in the ventral cochlear nucleus, often between endbulbs and bushy cells. Both "modified" endbulbs and the larger endbulbs of Held transneuronally labeled the bushy cells that they contacted. At the ultrastructural level, transneuronal labeling was evident as a darkening of ribosomes and the membrane surfaces of mitochondria, endoplasmic reticulum, and the nucleus. Transneuronal labeling occurred rarely in octopus, small, and stellate cells, and in neurons of the dorsal cochlear nucleus. Spiral ganglion injections also label olivocochlear fibers, efferent fibers that pass through the ganglion en route to the hair cells. These fibers give off branches to the cochlear nucleus that were rarely associated with transneuronal labeling. In eight instances, the targets of olivocochlear branches were stellate cells or small cells. We suggest that in our mouse preparation, horseradish peroxidase is effective as a transneuronal marker because the short distance from injection site to the cochlear nucleus results in a high concentration of horseradish peroxidase in the endings of the auditory nerve fibers.

Afferent Pathways↗
PubMed1998

PEP-19 immunoreactivity in the cochlear nucleus and superior olive of the cat.

We applied antiserum to PEP-19, a presumptive calcium-binding polypeptide, to the auditory brainstem of cats to determine whether this antiserum would selectively reveal cochlear nucleus neurons and their projections. We report that the entire populations of ventral cochlear nucleus bushy and multipolar cells, but not octopus cells, express this peptide in their somata and dendrites. Presumed axons of spherical bushy cells located dorsally and thicker globular bushy cell fibers located ventrally in the trapezoid body are immunostained, as are thin fibers presumed to represent the axons of multipolar cells. Large calyceal endings in the medial nucleus of the trapezoid body are densely immunoreactive as are smaller punctate profiles that outline immunonegative neuronal profiles in the medial and lateral superior olives. These features of immunolabeling indicate that PEP-19 is expressed in all neuronal compartments. Within the entire superior olivary complex, relatively few neurons are immunolabeled, and the vast majority of these are found in the periolivary nuclei. There are many more immunostained neurons in lateral than in medial periolivary cell groups, but their combined numbers are dwarfed by the numbers of immunolabeled cells in the ventral cochlear nucleus. The borders of the principal nuclei and some of the periolivary cell groups are well defined by the distribution of PEP-19-immunoreactive fibers and puncta. Since ventral cochlear nucleus bushy cells comprise the predominant input to principal nuclei of the superior olive, and the entire bushy cell population is immunolabeled by PEP-19 antiserum, the numbers and distribution of their inputs can be quantified. In this study we report that immunoreactive puncta apposed to the cell bodies and proximal dendrites of neurons in the medial superior olive occur at a density of 20/100 microns2. Moreover, we demonstrate by pre-embedding immunoelectron microscopy that the PEP-19-immunoreactive punctate profiles observed in the medial superior olive by light microscopy represent presynaptic terminal boutons that contain round synaptic vesicles and form asymmetric synaptic junctions, features traditionally associated with excitatory synapses. Thus, this antiserum represents a useful tool for investigating the distribution of ventral cochlear nucleus fibers and synaptic terminals within their target nuclei in the superior olive.

Animals↗
PubMed1999

Cochlear nerve projections to the small cell shell of the cochlear nucleus: the neuroanatomy of extremely thin sensory axons.

Labeling cochlear nerve fibers in the inner ear of chinchillas with biotinylated dextran polyamine was used to trace the thin fibers (Type II), which likely innervate outer hair cells. These axons, 0. 1-0.5 microm in diameter, were distinguished from the thicker Type I, fibers innervating inner hair cells, and traced to small-cell clusters in the cochlear nucleus. This study provided two major new insights into the outer hair cell connections in the cochlear nucleus and the potential significance of very thin axons and synaptic nests, which are widespread in the CNS. 1) EM serial reconstructions of labeled and unlabeled material revealed that Type II axons rarely formed synapses with conventional features (vesicles gathered at junctions). Rather, their endings contained arrays of endoplasmic reticulum and small spherical vesicles without junctions. 2) Type II axons projected predominantly to synaptic nests, where they contacted other endings and dendrites of local interneurons (small stellate and mitt cells, but not granule cells). Synaptic nests lacked intrinsic glia and, presumably, their high-affinity amino acid transporters. As functional units, nests and their Type II inputs from outer hair cells may contribute to an analog processing mode, which is slower, more diffuse, longer-lasting, and potentially more plastic than the digital processors addressed by inner hair cells.

Animals↗
PubMed1991

Effects of total cochlear haircell loss on integrity of cochlear nucleus. A quantitative study.

In cochleas of chincillas treated with amikacin, cochlear sensory cells were totally destroyed in all new-born animals. In animals treated as adults some occasional haircells remained in apical turns. In the neonatally treated animals, the resulting auditory deprivation significantly affected the volume of the ventral cochlear nucleus and large-dark spherical cell area. The density of large-dark spherical cells increased significantly from normal in both neonatally and adult treated groups. Our results suggest that the VCN is more dependent on auditory stimulation for proper development than the DCN. In adult chinchillas treated with amikacin there was a significant change in large-dark spherical cell density without a change in total cell numbers or large-dark spherical cell area volume. Our study indicates that the mature cochlear nucleus is much more resistant to the effects of auditory deprivation than the developing cochlear nucleus and that the maintenance of the mature auditory system is not as dependent on auditory stimulation. Studies such as this examining the morphological effects of profound cochlear deafness on higher levels of the auditory system are essential in cochlear implant research.

Amikacin↗
PubMed1994

A physiological and structural study of neuron types in the cochlear nucleus. II. Neuron types and their structural correlation with response properties.

The present study examined the morphological cell types of neurons labeled with intracellular horseradish peroxidase injections, many of them following electrophysiological recordings in the cochlear nucleus of gerbils and chinchillas. Most of the subdivisions and neuronal types previously described in the cat were identified in the present material, including spherical and globular bushy cells, stellate, bushy multipolar, elongate, octopus, and giant cells in the ventral cochlear nucleus, and a cartwheel cell in the dorsal cochlear nucleus. In many cases these structurally distinct neurons were correlated with their characteristic responses to stimulation by sound or intracellular injection of depolarizing current. The dendritic terminals of the elongate, antenniform, and clavate cells of the posteroventral cochlear nucleus link each of these cell types with neighboring structures in distinct patterns, which may provide a basis for differences in synaptic organization. These cell types differ from each other and from the stellate cells of the anteroventral cochlear nucleus. Despite their heterogeneous morphology, most of these neurons had a regular discharge in response to stimulation (choppers). Irregularly firing neurons (primary-like) had very different structures, e.g., the spherical and globular bushy cells and the bushy multipolar neuron. They, too, represent a heterogeneous population. An onset neuron was identified as an octopus cell. This paper compares the morphological observations with the electrophysiological properties of different cell types reported in a companion paper (Feng et al. [1994] J. Comp. Neurol.). Together, these findings imply that response properties may be partially independent of neuronal structure. Morphologically distinct neurons can generate similar temporal patterns in response to simple acoustic stimuli. Nevertheless, the synaptic organization of these different neuron types, including their connections, would be expected to affect or alter the cells' responses to appropriate stimuli. The possibility is raised that membrane properties and synaptic organization complement and interact with each other.

Animals↗
PubMed1983

Physiological response properties of cells labeled intracellularly with horseradish peroxidase in cat dorsal cochlear nucleus.

The physiology and morphology of fusiform cells in the dorsal cochlear nucleus were studied using extracellular and intracellular recording and intracellular injection of horseradish peroxidase. Fusiform cells displayed a variety of responses to tone pips presented at the characteristic frequency; most often these cells exhibited the pauser/buildup pattern defined in earlier studies. The response pattern of each neuron was dependent on frequency and sound-pressure level. Tone pips evoked short-lasting depolarizations of about 10 mV and long-lasting hyperpolarizations of about 10 mV in cells whose resting potentials were -50 to -65 mV. The time courses of both the excitation and the inhibition depended on frequency and sound-pressure level. Generally the depolarization was sustained for the duration of the tone pip, whereas the hyperpolarization could last as long as 600 ms after the end of the tone pip. Often a neuron exhibited a sustained chopper pattern after microelectrode impalement. This was probably a result of a decrease in membrane potential which altered the relative effectiveness of the excitatory and inhibitory inputs. The large, bitufted fusiform cells had many apical dendrites, which branched one to five times and were covered with spines, and fewer basal dendrites, which exhibited little branching and had few appendages. The morphology of fusiform cells varied systematically as a function of location within the dorsal cochlear nucleus. Response patterns for tone pips were not exclusive to individual cell types as two nonfusiform cells were found to exhibit a buildup pattern. Axons of injected neurons left the nucleus via the dorsal acoustic stria and 14 of 15 had collaterals within the dorsal cochlear nucleus.

Animals↗
PubMed1994

A physiological and structural study of neuron types in the cochlear nucleus. I. Intracellular responses to acoustic stimulation and current injection.

Neurons in the cochlear nucleus differ in their discharge patterns when stimulated by tones. They also differ in their responses to depolarizing current injection in vitro. We made intracellular recordings from neurons in the cochlear nucleus of gerbils and chinchillas. The responses to tones and to depolarizing current were compared for the same neurons. Three categories of response patterns to tones were observed: chopper, primary-like, and onset. Chopper neurons responded with regularly spaced action potentials to stimulation with tones and to injections of depolarizing current. Their response rate rose with increasing levels of current to a maximum, which was comparable to that evoked by suprathreshold tones. These observations suggest that the regularity and maximal firing rate of these neurons are determined by voltage-dependent membrane properties. Primary-like neurons responded with irregularly spaced action potentials to tones. Injection of depolarizing current into these neurons produced a single action potential at current onset, which could be followed by a few irregularly spaced action potentials. The response rate showed little relation to current level. These data suggest that the membrane characteristics of primary-like neurons are different from those of chopper neurons. Onset neurons produced action potentials only at the beginning of the stimulus for both tones and depolarizing current, even though there was a sustained depolarization throughout the duration of the tone. The findings suggest that cochlear nucleus neurons have different membrane properties and that these properties may play a critical role in a neuron's temporal response pattern to acoustic stimulation.

Acoustic Stimulation↗
PubMed2004

Fine structure of degeneration in the cochlear nucleus of the chinchilla after acoustic overstimulation.

To study plastic changes in the cochlear nucleus after acoustic stimulation, adult chinchillas were exposed once to a 4-kHz octave-band noise at 108 dB SPL for 3 hr. After survival times of 1, 2, 4, 8, and 16 weeks, samples were taken for electron microscopy from a part of the cochlear nucleus, where cochlear nerve fibers degenerated after the noise exposure. Progressive changes in fine structure were characterized as early, intermediate, and late stages of degeneration. Freshly occurring synaptic degeneration appeared in each period from 1-16 weeks. Endings with large round vesicles, putative excitatory synapses of the cochlear nerve, displayed progressive increases in neurofilaments and enlarged synaptic vesicles. Compared to controls, synaptic vesicles seemed fewer, often in small clusters in the interior of endings, and smaller in the synaptic zone. These early changes progressed to mitochondrial disintegration and overt "watery" degeneration. Some surviving endings, however, were shrunken and displaced partially by enlarged spaces in the synaptic complex. Dense-cored vesicles gathered in these endings. In terminals with pleomorphic and flattened vesicles, presumed inhibitory endings, cytological changes appeared within 1 week and persisted for months. The synaptic endings darkened, some vesicles disintegrated, and many smaller flatter vesicles collapsed into heaps. Especially at the presynaptic membrane, vesicles were shriveled, but a few mitochondria were preserved. Without overt signs of synaptic degeneration, some of these cytological changes presumably reflect reduced synaptic activity in the inhibitory endings. These changes may contribute to a continuing process associated with abnormal auditory functions, including hyperacusis and tinnitus.

Acoustic Stimulation↗