Cat Dorsal Cochlear Nucleus Research Articles

A Modeling Study of Notch Noise Responses of Type III Units in the Gerbil Dorsal Cochlear Nucleus

A computational model of the neural circuitry of the gerbil dorsal cochlear nucleus (DCN), based on the MacGregor’s neuromime model, was used to simulate type III unit (P-cell) responses to notch noise stimuli. The DCN patch model is based on a previous computational model of the cat DCN [Hancock, K. E., and H. F. Voigt. Ann. Biomed. Eng. 27:73–87, 1999]. According to the experimental study of Parsons et al. [Ann. Biomed. Eng. 29:887–896, 2001], the responses of gerbil DCN type III units to notch noise stimuli are similar to those of cat DCN type IV units, which are thought to be spectral notch detectors. This suggests that type III units in the gerbil DCN may serve as spectral notch detectors. In this modeling study, a simplified notch noise response plot—spike discharge rate vs. notch cutoff frequency plot—was used to compare model responses to the experimental results. Parameter estimation and sensitivity analysis of three connection parameters within the DCN patch have been studied and shows the model is robust, providing reasonable fits to the experimental data from 14 of 15 type III units examined [work supported by a grant from NIDCD, Boston University’s Biomedical Engineering department and Hearing Research Center].

Computational model of response maps in the dorsal cochlear nucleus

The neurons in the mammalian (gerbil, cat) dorsal cochlear nucleus (DCN) have responses to tones and noise that have been used to classify them into unit types. These types (I-V) are based on excitatory and inhibitory responses to tones organized into plots called response maps (RMs). Type I units show purely excitatory responses, while type V units are primarily inhibited. A computational model of the neural circuitry of the mammalian DCN, based on the MacGregor neuromime, was used to investigate RMs of the principal cells (P-cells) that represent the fusiform and giant cells. In gerbils, fusiform cells have been shown to have primarily type III unit response properties; however, fusiform cells in the cat DCN are thought to have type IV unit response properties. The DCN model is based on a previous computational model of the cat (Hancock and Voigt Ann Biomed Eng 27: 73-87, 1999) and gerbil (Zheng and Voigt Ann Biomed Eng 34: 697-708, 2006) DCN. The basic model for both species is architecturally the same, and to get either type III unit RMs or type IV unit RMs, connection parameters were adjusted. Interestingly, regardless of the RM type, these units in gerbils and cats show spectral notch sensitivity and are thought to play a role in sound localization in the median plane. In this study, further parameter adjustments were made to systematically explore their effect on P-cell RMs. Significantly, type I, type III, type III-i, type IV, type IV-T and type V unit RMs can be created for the modeled P-cells. Thus major RMs observed in the cat and gerbil DCN are recreated by the model. These results suggest that RMs of individual DCN projection neurons are the result of specific assortment of excitatory and inhibitory inputs to that neuron and that subtle differences in the complement of inputs can result in different RM types. Modulation of the efficacy of certain synapses suggests that RM type may change dynamically.

A Modeling Study of Notch Noise Responses of Type III Units in the Gerbil Dorsal Cochlear Nucleus

A computational model of the neural circuitry of the gerbil dorsal cochlear nucleus (DCN), based on the MacGregor's neuromime model, was used to simulate type III unit (P-cell) responses to notch noise stimuli. The DCN patch model is based on a previous computational model of the cat DCN [Hancock, K. E., and H. F. Voigt. Ann. Biomed. Eng. 27:73-87, 1999]. According to the experimental study of Parsons et al. [Ann. Biomed. Eng. 29:887-896, 2001], the responses of gerbil DCN type III units to notch noise stimuli are similar to those of cat DCN type IV units, which are thought to be spectral notch detectors. This suggests that type III units in the gerbil DCN may serve as spectral notch detectors. In this modeling study, a simplified notch noise response plot-spike discharge rate vs. notch cutoff frequency plot-was used to compare model responses to the experimental results. Parameter estimation and sensitivity analysis of three connection parameters within the DCN patch have been studied and shows the model is robust, providing reasonable fits to the experimental data from 14 of 15 type III units examined [work supported by a grant from NIDCD, Boston University's Biomedical Engineering department and Hearing Research Center].

Isoflurane/N 2O anesthesia suppresses narrowband but not wideband inhibition in dorsal cochlear nucleus

Anesthesia alters the response properties of neurons in the dorsal cochlear nucleus (DCN). Barbiturates decrease spontaneous activity and the prevalence of inhibitory responses, so that DCN principal cells show less inhibition by narrowband stimuli (e.g. tones at best frequency). Here we present the effects on cat DCN of anesthesia using isoflurane plus nitrous oxide (N 2O). Because the cellular anesthetic mechanisms of isoflurane differ from those of pentobarbital, the effects of the two anesthetics in DCN might be different. The strength of two inhibitory circuits in the DCN, the narrowband and wideband inhibitor, were studied and compared with results in unanesthetized decerebrate animals. The primary effects of isoflurane/N 2O anesthesia were to lower spontaneous activity and increase the thresholds of units. All the response types seen in the decerebrate preparation were also seen with isoflurane/N 2O, but the prevalence of predominantly inhibitory responses to narrowband stimuli (type IV units) decreased (from ∼31% to ∼11%). However, responses to band-reject noise were similar to those seen in unanesthetized animals. Together, these results suggest that the effects of isoflurane/N 2O are primarily on the narrowband inhibitory circuit, rather than the wideband inhibitor.

Proprioceptive Information from the Pinna Provides Somatosensory Input to Cat Dorsal Cochlear Nucleus

The dorsal cochlear nucleus (DCN) is a second-order auditory structure that also receives nonauditory information, including somatosensory inputs from the dorsal column and spinal trigeminal nuclei. Here we investigate the peripheral sources of the somatosensory inputs to DCN. Electrical stimulation was applied to cervical nerves C1-C8, branches of C2, branches of the trigeminal nerve, and hindlimb nerves. The largest evoked potentials in the DCN were produced by C2 stimulation and by stimulation of its branches that innervate the pinna. Electrical stimulation of C2 produced a pattern of inhibition and excitation of DCN principal cells comparable with that seen in previous studies with stimulation of the primary somatosensory nuclei, suggesting that the same pathway was activated. Because C2 contains both proprioceptive and cutaneous fibers, we applied peripheral somatosensory stimulation to identify the effective somatosensory modalities. Only stimuli that activate pinna muscle receptors, such as stretch or vibration of the muscles connected to the pinna, were effective in driving DCN units, whereas cutaneous stimuli such as light touch, brushing of hairs, and stretching of skin were ineffective. These results suggest that the largest somatosensory inputs to the DCN originate from muscle receptors associated with the pinna. They support the hypothesis that a role of the DCN in hearing is to coordinate pinna orientation to sounds or to support correction for the effects of pinna orientation on sound-localization cues.

Type III units in the gerbil dorsal cochlear nucleus may be spectral notch detectors.

Broadband sounds originating in the median plane are thought to be localized by neural processing of spectral notches introduced by the filtering action of the pinnae. Previous studies (Nelken, I., and E. D. Young. J. Neurophysiol. 71:2446-2462, 1994: Spirou, G. A., and E. D. Young. ibid. 66: 1750-1768. 1991) suggested that type IV units in decerebrate cat dorsal cochlear nucleus (DCN) are functional detectors of these spectral notches. Intracellular marking studies by Ding et al. (Ding, J., T. E. Benson, and H. F. Voigt. J. Neurophysiol. 82:3434-3457, 1999) have shown that type III units in gerbil arise from the DCN's principal output neurons, which are thought to have type IV unit properties in cat. A relative paucity of type IV units in the decerebrate gerbil (Davis. K. A., J. Ding, T. E. Benson, and H. F. Voigt. J. Neurophysiol. 75: 1411-1431, 1996) has motivated this study of spectral notch sensitivity in the gerbil DCN. Responses to notch noise stimuli were recorded from 15 gerbil type III units to investigate whether these units may function as spectral notch detectors. For narrow notch noise stimuli, all 15 units showed excitatory responses. For progressively wider notches, the discharge rate of 13/15 units became inhibited. As the maximum limits of notch width were approached, 11/15 units showed some degree of recovery from this inhibition. This response pattern in gerbil type III units possesses the salient features of notch noise responses in cat type IV units and implicates type III units in gerbilline spectral notch detection processes.

Vertical cell responses to sound in cat dorsal cochlear nucleus.

The dorsal cochlear nucleus receives input from the auditory nerve and relays acoustic information to the inferior colliculus. Its principal cells receive two systems of inputs. One system through the molecular layer carries multimodal information that is processed through a neuronal circuit that resembles the cerebellum. A second system through the deep layer carries primary auditory nerve input, some of which is relayed through interneurons. The present study reveals the morphology of individual interneurons and their local axonal arbors and how these inhibitory interneurons respond to sound. Vertical cells lie beneath the fusiform cell layer. Their dendritic and axonal arbors are limited to an isofrequency lamina. They give rise to pericellular nests around the base of fusiform cells and their proximal basal dendrites. These cells exhibit an onset-graded response to short tones and have response features defined as type II. They have tuning curves that are closed contours (0 shaped), thresholds approximately 27 dB SPL, spontaneous firing rates of approximately 0 spikes/s, and they respond weakly or not at all to broadband noise, as described for type II units. Their responses are nonmonotonic functions of intensity with peak responses between 30 and 60 dB SPL. They also show a preference for the high-to-low direction of a frequency sweep. It has been suggested that these circuits may be involved in the processing of spectral cues for the localization of sound sources.

Facilitation of acoustic responses of cartwheel neurons of the cat dorsal cochlear nucleus.

Responses to clicks were increased in cartwheel cells of the dorsal cochlear nucleus of cats after pairing presentations of the clicks with local iontophoretic delivery of glutamate. The cells were identified by bursting discharges, and were recorded intracellularly in vivo. The findings indicate that inhibitory interneurons such as cartwheel cells can participate in complex adaptive acoustic signal processing. Each cell displayed doublet discharges of > 800 Hz. In 70% of the cells, some of the doublet discharges reached rates > 1000 Hz.

A computational model for signal processing by the dorsal cochlear nucleus. I. Responses to pure tones

Much information is available on the anatomical organization and neurophysiological properties of the major cell types in the dorsal cochlear nucleus (DCN). The complicated response properties of individual cells and units in the DCN indicate that substantial information processing already occurs at the level of the DCN. A large number of connectional hypotheses have been put forward to explain various aspects of the response characteristics of DCN cells, but many of the consequences of these hypotheses have not been investigated quantitatively. In this paper, we investigate these hypotheses by constructing and testing mathematical and computational models and compare our results to those of previous modeling studies. The simplest versions of our models include auditory nerve (AN) fibers, type II cells (inhibitory interneurons) and type IV cells (fusiform and giant cells). The model response maps, i.e., the pattern of output of model type IV cells, generated by the simplest model have some but not all the features of the experimental response maps of type IV neurons. In particular, the excitatory region which occurs at best frequency is not isolated and the excitatory region at low frequencies and high amplitude is narrower than observed. Since experimental evidence exists that some of the connections between these cell types are divergent or convergent across adjacent isofrequency sheets, the effect of such convergence and divergence was then investigated. Response maps so obtained reproduce many of the qualitative features of the experimental maps. Enlargement of the model by including inhibitory interneurons (e.g., stellate cells) that receive convergent input from AN fibers and which inhibit type II cells results in the generation of response maps that, with some variations in connectional patterns and physiological properties of neurons, match most of the essential features seen in the large variety of experimental maps obtained from the cat DCN.

Development of GAD-immunoreactivity in the dorsal cochlear nucleus of the hamster and cat: light and electron microscopic observations

Physiologic and pharmacologie evidence suggests that inhibitory influences are active in the mammalian dorsal cochlear nucleus (DCN) by the onset of hearing, while anatomical evidence suggests that inhibitory synapses are not present until days or weeks later. One inhibitory neurotransmitter in the DCN is gamma aminobutyric acid (GABA) and its presence can be indexed by immunohistochemical localization of its synthetic enzyme glutamic acid decarboxylase (GAD). The present study investigated the ingrowth and synapse formation of GAD-immunoreactive inputs in the DCN of cat and hamster. GAD-immunoreactive puncta are present in the DCN of the cat at birth and of the hamster on postnatal day (PND) 3. Thus, the present data correlate well with the physiologic and pharmacologie evidence. In both species the first labelled puncta are near the dorsal acoustic stria and may originate from efferent axons in the stria. Several days later a band of labelled puncta is found in the fusiform cell layer. This location is equivalent to the termination zone of cartwheel cells, GAD- immunoreactive interneurons in the DCN. Based on this spatiotemporal sequence in the appearance of GAD-immunoreactive puncta, we suggest that sources of GABA extrinsic to the DCN mature first, followed by intrinsic sources.

Organization of dorsal cochlear nucleus type IV unit response maps and their relationship to activation by bandlimited noise

1. Response maps of 49 type IV neurons in cat dorsal cochlear nucleus (DCN) were studied by moving a tone in small steps along the frequency dimension and along the intensity dimension. Type IV responses are recorded from DCN principal cells. Data were collected from 38 units with best frequencies (BFs) from 2.16 to 50.3 kHz with the use of electrode penetrations along the long (strial) axis of the DCN; an additional 11 units from a previous study were analyzed. A stereotypical type IV response map is defined as consisting of two excitatory and two inhibitory regions. Type IV units from both the pyramidal cell layer (probably pyramidal cells) and the deep layer (probably giant cells) show the same types of response maps. 2. Two of the regions, one excitatory and one inhibitory, are seen in all type IV units. These regions are a low-threshold excitatory region at best frequency (BFER) and an inhibitory area at higher levels, usually centered below BF but extending upward in frequency to include BF (central inhibitory area, or CIA). The high resolution of the response maps in this paper allows us to show that type IV units fall into two groups on the basis of whether their CIAs are narrow with well-defined borders (35 units) or broad with poorly defined borders (14 units). 3. Two additional features of type IV response maps can be defined, most consistently in units with well-defined CIAs. These features are an excitatory region along the high-frequency edge of the CIA (upper excitatory region, UER) and an upper inhibitory sideband (UIS). The BFER and UER are continuous in many units, but in some cases their continuity is broken by the CIA. It seems likely that the BFER and UER represent a single excitatory input to type IV units and are revealed because the tuning curve of the stronger inhibitory inputs that produce the CIA has thresholds greater than and BFs lower than the excitatory inputs. 4. The CIA is probably produced by inhibitory inputs from DCN type II neurons. The bandwidths of type IV CIAs are about 1-3 times larger (at 40 dB above threshold) than the excitatory bandwidths of DCN type II units, suggesting a convergence of the equivalent in tuning of about two type II units onto each type IV unit. The BF of the CIA is below the excitatory BF of the type IV unit in most cases.(ABSTRACT TRUNCATED AT 400 WORDS)

Cross-correlation analysis of inhibitory interactions in dorsal cochlear nucleus

1. Cross-correlation analysis was used to study the organization of inhibitory connections between type II or type III units and type IV principal cells in cat dorsal cochlear nucleus (DCN). Pairs of units were isolated using two microelectrodes so that information about the distance over which connections are made could be analyzed. Data were obtained from 51 pairs consisting of a type II and a type IV unit and from 22 pairs consisting of a type III and a type IV unit. The analyses in this paper concentrate on type II-type IV pairs. 2. Inhibitory troughs (ITs) are observed in the cross-correlograms of type II-type IV pairs (21/51 cases). An IT is a transient decrease in discharge probability in the postsynaptic (type IV) unit immediately after spikes in the presynaptic unit (type II). The average latency to the start of ITs is 0.73 ms, and the troughs are asymmetric with a faster leading phase. Small excitatory peaks accompany the ITs in type II units, but these are probably secondary effects associated with the IT. ITs are consistent with a monosynaptic, inhibitory connection between type II and type IV units. A variety of evidence suggests that type II responses are recorded from vertical cells, an interneuron in the deep layer of the DCN that may be glycinergic. 3. The cross-correlograms of type III-type IV pairs are more complex and variable than those of type II-type IV pairs--ITs are seen in 4/22 cases, and peaks of correlation that are symmetrically located around the origin (central mound or CM) are seen in 4/22 cases; two cases have both an IT and a CM. CMs result from shared sources of input. Whereas type II-type IV correlogram features change primarily in amplitude as stimulus conditions change, correlogram features in some type III-type IV pairs change qualitatively with stimulus conditions; correlograms are flat for some stimuli and show ITs or CMs or mixtures of the two for others. This variability suggests that the circuitry associated with type III-type IV pairs is more complex than a monosynaptic connection, and further analysis of type III-type IV pairs was not done. 4. The strength of inhibition for an IT is measured as the area under the IT (effectiveness) and as effectiveness divided by the postsynaptic discharge rate (association index).(ABSTRACT TRUNCATED AT 400 WORDS)

Physiological studies on neurons in the dorsal cochlear nucleus of cat.

Results reported here support the conclusion that an individual neuron in the dorsal cochlear nucleus (DCN) can exhibit pauser, buildup, and chopper patterns in response to tone pips. Fusiform cells have been previously identified as the principal cell exhibiting these patterns. Fusiform cells can also exhibit an onset response followed by suppression of spontaneous activity at their characteristic frequency (CF). Off CF only suppression is seen. These neurons are characterized by a restricted excitatory region near threshold. All these cells can exhibit nonmonotonic rate curves, narrow excitatory regions, and inhibitory sidebands. Nonmonotonicity occurred in 34% of pausers, 52% of buildup, 89% of onsets with a graded response, and 50% overall in the DCN cells. Chopper units occur as often as the other types combined in the DCN. Only 14% show nonmonotonic rate curves. Those with high-spontaneous activity also show inhibitory sidebands. Cells with a predominant buildup pattern occur most frequently in the fusiform cell layer, whereas pausers occur throughout the DCN below the molecular layer. Intracellular potentials often reflect the average response pattern. Sharply delimited response areas indicate that these cells may be useful for performing a spectral analysis. These cells show almost no phase locking suggesting that temporal encoding is an unlikely function. It is suggested that the effects of anesthetic on the function of the DCN is not as marked as previously indicated.

Electron microscopic features of physiologically characterized, HRP-labeled fusiform cells in the cat dorsal cochlear nucleus.

We report on the anatomy and physiology of three fusiform cells in the dorsal cochlear nucleus (DCN) of the cat. The extra- and intracellular responses of these cells to pure tones showed features typical of the cell type. Peristimulus time histograms (PSTHs) were usually of the pauser or buildup configuration with chopping behavior noted in certain instances. Intracellular records during stimulus presentations revealed sustained depolarizations for the duration of the tone followed by a prolonged after-hyperpolarization (AHP). On rare occasions, a hyperpolarization corresponding to the pause region of the PSTH was noted. Occasionally, a stimulus-induced depolarization would be maintained after stimulus offset. Rebound excitation was also observed after the AHP. Morphologically, all three cells showed the standard fusiform cell features at the light microscopic level. The cell body gave rise to apical and basal dendritic trees. The apical tree branched frequently and displayed numerous spines distally. The basal tree had fewer branches and fewer, more irregular appendages. The axon originated from the cell body and gave rise to one or more collaterals before leaving the nucleus via the dorsal acoustic stria (DAS). At the electron microscopic (EM) level, the axon collaterals may terminate on a variety of cell types in the DCN, including fusiform cells. Their vesicles are round and the terminals closely resemble many unlabeled terminals seen on the cell body and apical and basal dendrites of our labeled fusiform cells. Terminals containing round vesicles, believed to be eighth nerve terminals, were found, with one exception, only on the basal dendrites. The spine-laden, distal apical dendrites received primarily terminals containing round vesicles, presumed to originate from the unmyelinated axons of granule cells. The cell body and unmyelinated initial segment received mostly terminals containing pleomorphic and flat vesicles, which also made up a large percentage of the dendritic input. Some relevant correlations, between the distribution of synaptic terminals and the observed physiology, may be possible.

Synaptic organization of eighth nerve afferents to cat dorsal cochlear nucleus.

The synaptic organization of eighth nerve afferents to the dorsal cochlear nucleus (DCN) of cats was studied using extracellular field potential analyses. The eighth nerve was electrically stimulated and potentials produced in the DCN characterized using single shocks, paired shocks, repetitive stimulation, and one-dimensional current source-density (CSD) analysis. Field potentials and CSD profiles were correlated with the laminated cytoarchitecture of the DCN. At least four major temporally discrete components can be identified in field potentials evoked by a single shock to the eighth nerve. The amplitude and polarity of these events depends on the layers in which they are recorded. A brief positive-negative deflection (the P1-N1) is present in all layers but is maximal in the deeper layers 3 and 4. The N1 has a peak latency of approximately 0.8 ms in these layers. The N1 in the deep layers is followed by a large negative potential, termed the N2, with a peak latency of about 1.6 ms. In the superficial layers (1 and 2), the N1 is followed by a small positive potential (the P2) occurring nearly simultaneously with the N2, Immediately following the N2 is another negative potential that is most clearly observed in layer 2. The layer 2 negative wave is termed N3 and is also identifiable on the repolarizing phase of the N2 in layers 3 and 4. The N3 in layer 2 can be followed by a positive potential, the P4. Simultaneous with the P4 is a small negative wave ion layer 1, termed the N4. The P4-N4 complex is observed in about half the recordings. Frequency-following tests indicate that both the N1 and N2 waves can follow shock trains up to 333 Hz. The N1 remains nearly constant in amplitude up to about 300 Hz and decreases as the stimulus frequency is raised to 500 Hz. The N2 decrements more rapidly than the N1 at frequencies above about 250 Hz and is considerably reduced at 500 Hz. The N2 sometimes shows an increased amplitude (by about 20-40%) between 100 and 250 Hz. A paired-shock paradigm was used to characterize further potentials. The N1 was little affected by prior stimulation for intervals greater than 5 ms. The N2 and N3 generally showed a small facilitation for shock intervals from about 7 to 30 ms, with a return to base line at longer intervals. The N4 and P4 (when present) were profoundly depressed for intervals from 7 to about 30 ms, with recovery to control values by 50 ms.(ABSTRACT TRUNCATED AT 400 WORDS)

Acoustic response properties of units in dorsal cochlear nucleus of unanesthetized, decerebrate gerbil

Single unit recordings were made in the dorsal cochlear nucleus (DCN) of unanesthetized, decerebrate Mongolian gerbils. Access to the gerbil DCN was obtained using a newly described approach [Frisina et al., Hearing Res. 6, 259 (1982)]. Single units, recorded with 3M NaCl filled micropipette electrodes (20 Mohm typical), were classified into three types (II, III, or IV) based on their responses to best frequency (BF) tone bursts and their rates of spontaneous discharges. Type II units have little or no spontaneous activity and are excited by BF tones at all levels above threshold. Type III units are also excited by BF tones at all levels above threshold, but have spontaneous activity rates that exceed 2.5 spikes/s. Type IV units are excited over a narrow range of sound levels near BF threshold, but are strongly inhibited at higher levels. Thus all unit types found in the unanesthetized, decerebrate cat DCN [Young and Brownell, J. Neurophysiol. 39, 282 (1976); Young and Voigt, Hearing Res. 6, 153 (1982)] are also found in gerbil. [Work supported by NIH.]

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.

Descending inputs to the cat dorsal cochlear nucleus: an electron microscopic study.

This experimental study provides identification of several types of terminals in the fusiform cell layer (FCL) of the cat dorsal cochlear nucleus (DCN). Eight types of synaptic terminal were defined in control animals. 22 experimental cats were then subjected to unilateral lesions of the superior olivary complex or SOC (Groups I and II), the inferior colliculus or IC (Groups III and IV), or the IC plus the dorsal nucleus of the lateral lemniscus or DNLL (Groups V and VI). After one to 14 days, animals were killed by perfusion-fixation and brain stems prepared for light and electron microscopic study of degeneration. After SOC lesions, the ipsilateral FCL showed degeneration of small (type 2a) endings on small dendritic shafts; the contralateral FCL showed degeneration of larger (type 5) endings mostly on fusiform cell somata and on some primary dendrites. Both sides showed mild degeneration of large, glomerular (type 1a) endings. After small IC lesions, the ipsilateral FCL demonstrated degenerating type 1a glomerular endings but the contralateral FCL showed severe degeneration of type 5a terminals (axodendritic to fusiform cells) and mild degeneration of both glomerular (type 1a) and axosomatic (type 5) endings. Combined IC-DNLL lesions caused extensive degeneration in a pattern similar to that following IC lesions. In addition retrograde degeneration of fusiform cells occurred bilaterally. These studies showed that: (1) type 2a endings originate in the ipsilateral SOC; (2) type 5 endings on fusiform cell bodies originate from the contralateral SOC; (3) type 5a endings on fusiform cell dendrites originate from the contralateral IC; and (4) type 1a glomerular endings probably arise from several sources, including the IC, the SOC and (possibly) the DNLL of both sides.

Desending and intrinsic inputs to dorsal cochlear nucleus of cats: A horseradish peroxidase study

Horseradish peroxidase was injected unilaterally into the dorsal cochlear nucleus of adult cats in efforts to find neurons innervating the dorsal cochlear nucleus from (1) higher auditory nuclei or (2) other subdivisions of the cochlear nucleus. Following horseradish peroxidase injections and short survival periods, reactive neurons were most common in the dorsal and ventral nuclei of the lateral lemniscus and in the superior olivary complex of both sides of the brain stem. In the superior olivary complex, most neurons of the medial segment and border cells of the lateral segment reacted as did periolivary cells of the ventrolateral, dorsomedial, and preolivary areas, but not in the medial nucleus of the trapezoid body. Hilus neurons of the lateral superior olive reacted contralateral to the injection site. Although inferior colliculus neurons contained lightly stained granules bilaterally, more reactive neurons (including unusually large tripolar neurons) contained heavily stained granules in the contralateral colliculus. Intrinsic reactive neurons mainly included ipsilateral octopus cells, multipolar neurons of the nerve root regions, and stellate cells of the more rostra] anteroventral cochlear nucleus. All findings were confirmed by comparison to control animals. Our findings of specific neuronal types projecting to the cat dorsal cochlear nucleus suggest a relatively greater input from the nuclei of the lateral lemnisci of both sides than previously believed. Also, our results showed an unusually heavy input from the nearby superior olivary complex to the dorsal cochlear nucleus as well as inputs from specific cell types of the ipsilateral antero- and postero-ventral cochlear nucleus. By correlating these findings with those of other types of studies, we concluded that (1) too much emphasis has been placed upon inputs to the dorsal cochlear nucleus from the inferior colliculus relative to the descending pontine inputs and that (2) a new circuit involving the ventral cochlear nucleus, the dorsal cochlear nucleus and the medial superior olive may provide binaural information to large dorsal cochlear nucleus cells that terminate in their own unique areas of higher auditory nuclei.

Synaptic organization in the dorsal cochlear nucleus of the cat: a light and electron microscopic study.

AbstractThis report describes some observations of the synaptic organization of one region of the cat dorsal cochlear nucleus (DCN). The large “fusiform cell” and its innervation from the cochlea are emphasized. The morphology of the mature fusiform cell and its postnatal development are described in rapid Golgi impregnations of perfusion‐fixed littermate cats. The mature features are correlated with profiles of fusiform cell bodies, apical dendrites, and basal dendritic trunks in electron micrographs from adult cat brains. Small neurons and granule cells are also identified in electron micrographs. In Golgi impregnations, axons of small cells and granule cells may terminate upon fusiform cells. Six classes of axons can be distinguished in rapid Golgi impregnations of the DCN. Two classes are of cochlear origin. One axonal class arises from small cells. The sources of the remaining axonal classes have not been identified in this study. Primary afferents can terminate as large, mossy endings in the DCN neuropil. They can also participate in axonal nests along with axons and dendrites of small cells. In electron micrographs, four synaptic endings can be distinguished. Primary cochlear fibers end in large terminals with asymmetrical synaptic complexes and round, clear vesicles. Primary axons can end in glomeruli, resembling those of the cerebellum, or in synaptic nests which are conglomerates of neuronal processes including other types of endings. The origins of the other synaptic types are not yet known. According to this study, primary afferent input could influence fusiform cells directly or indirectly, via small cells and granule cells.