Response patterns to sound associated with labeled globular/bushy cells in cat.

The mammalian cochlear nucleus (CN) consists of a diverse set of neurons both physiologically and morphologically that are involved in processing different aspects of the sound signal. One class of CN neurons that is located near the entrance of the auditory nerve (AN) to the CN has an oval soma with an eccentric nucleus and a short-bushy dendritic tree and is called a globular/bushy cell (GBC). They contact the principal cells of the medial nucleus of the trapezoid body (MNTB) with the very large calyx of Held that is one of the most secure synapses in the brain. Because MNTB cells provide an inhibitory input to the lateral superior olive (LSO), a structure purported to play a role in lateralizing high frequency sounds, GBC physiology is of great interest. Results were obtained with intracellular recording and subsequent labeling with neurobiotin of 32 GBCs along with a number of cells characterized extracellularly as likely GBCs in the cochlear nucleus (CN) of cat. Their poststimulus discharge response pattern to repeated tones varies from a primarylike pattern, i.e. similar to the AN, to a primarylike pattern with a 0.5-2 ms notch after the initial spike, to an onset pattern with a low-sustained rate. They can represent low frequency tones and amplitude modulated signals exceptionally well with a temporal code.

Characterization of HRP-labeled globular bushy cells in the cat anteroventral cochlear nucleus.

We report on the anatomical and physiological features of globular bushy cells in the posterior division of the anteroventral cochlear nucleus based on the characteristics of 20 cells from this population. Each of these cells was recorded from and characterized intracellularly and/or extracellularly, injected with horseradish peroxidase, and studied at the light and/or electron microscopic level. Intracellular records from the vicinity of the globular bushy cell body displayed large, fast synaptic potentials, and in some instances a larger presumed action potential both in silence and during short tone stimulation. Intraaxonal recordings displayed large action potentials in addition to small, fast potentials, which evidence indicates may be the decrementally conducted subthreshold synaptic potentials. Both recording situations indicated that these auditory nerve inputs need not be suprathreshold. Bushy cells with high characteristic frequencies (CFs greater than 3 kHz) typically showed primary-like-with-notch responses to short tones at CF or on-type L responses if the sustained level of discharge after the notch was not as robust. Low-CF bushy cells phase-locked after a well-timed onset spike. Light microscopic anatomy revealed a typically oval cell body giving rise to one or two primary dendrites that branched profusely and an axon that gave off no collaterals within the cochlear nucleus before entering the trapezoid body. Electron microscopic analysis showed a high concentration of large, round, vesicle-containing terminals on the cell body and primary dendrite while the population of terminals on the initial segment and sparsely covered distal dendrites was made up mostly of flat and pleomorphic vesicle-containing terminals.

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.

Structural and functional properties distinguish two types of multipolar cells in the ventral cochlear nucleus.

We distinguish two types of large multipolar cells designated sustained (CS) and onset (OC) choppers in the anterior posteroventral cochlear nucleus (A-PVCN)/nerve root region on the basis of certain anatomical and physiological features. CS axons head into the trapezoid body, while OC axons use the intermediate acoustic stria of Held. At the electron microscopic (EM) level, collateral terminals of OC axons contain pleomorphic vesicles; CS terminals contain small round vesicles. CS dendritic trees tend to be distributed in a stellate fashion while OC dendritic trees tend to be elongated. At the EM level the sustained chopper somata are sparsely innervated while the proximal dendritic tree receives considerably more input. The OC somata are highly innervated and this heavy innervation continues out onto the proximal dendrites. Distally the dendritic innervation falls off considerably for both categories. Physiologically, members of the OC population have wider dynamic ranges at the characteristic frequency (CF), wider response areas that are typically not flanked by inhibitory sidebands, and responses to short tones that do not show the same form of regularity expressed by sustained choppers. Intracellularly the sustained choppers exhibit sustained depolarization to short tones for the duration of the stimulus with resultant regular spiking at a rate that is stimulus level dependent. The response to swept tone shows this same level-dependent regularity. In response to tones, the OC cells also show a sustained depolarization whose amplitude is stimulus-level dependent but whose range is much greater and whose onset is initiated more abruptly. Although the onset component of the OC spike output is reliably initiated by these levels of depolarization, regular firing to the sustained depolarization is not initiated at levels of depolarization that would surely generate regular firing in sustained choppers. This regularity is also absent in the swept tone response despite marked levels of excitation.

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.

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

To determine the correspondence between anatomical and physiological cell types in the ventral cochlear nucleus of the cat, intracellular injections of horseradish peroxidase were made into cells whose extracellular and intracellular responses to sound had been studied. Three identified cells responded to a short tone burst at their characteristic frequencies with an onset pattern. This pattern is characterized by a strong response to the onset of the stimulus. One was an octopus cell. The second cell, located in the octopus-cell area, was a giant cell with a few somatic spines and thin tapering dendrites; the intracellular record revealed that even in the absence of sound it received continuous synaptic input, while tones at characteristic frequency produced a sustained depolarization. A third cell, which had an onset response at low intensities and a chopper response at high intensities, was a stellate cell located in the intermediate acoustic stria with dendrites oriented parallel to the fiber tract. This cell had an unusually broad dynamic range in response to changes in intensity. Two cells with transient chopper response patterns were stellate cells in the posteroventral cochlear nucleus with many branched and beaded dendrites. Three cells with more sustained chopper response patterns were stellate cells in the anteroventral cochlear nucleus with fewer, less-branched, smooth dendrites. Two cells with primarylike responses to tones were bushy cells with numerous short, thin, highly branched dendrites in the posterior division of the anteroventral cochlear nucleus. Intracellular responses to tones at the characteristic frequency consisted of large brief depolarizations, which were not sustained. Another cell, which responded to tones in a phase-locked fashion, was also located in the anteroventral cochlear nucleus. It was a small, stellate cell with relatively few, smooth dendrites. The labeled cells largely support previous attempts at physiological-morphological correlations: (1) bushy cells exhibit primarylike pattern; (2) stellate cells exhibit chopper patterns; and (3) octopus cells exhibit an onset pattern. It was also demonstrated that more than one cell type can exhibit a particular response pattern.

Visual evoked spectrum array and interhemispheric variations.

An EEG spectrum analysis during visual stimulation was computed in 19 normal subjects. Visual stimulation consisted of trains of flashes at frequencies ranging between 2.5 and 20 flashes per second. Recordings were carried out simultaneously from the right and left occipital regions with bipolar and referential montages. Compressed spectral arrays were computed for eight-second epochs at each recording site using a fast Fourier transform. The ratio of the spectral energy from homologus regions of right and left hemispheres at each stimulation frequency was determined. The ratios were graphically displayed in a visual evoked spectrum array (VESA) ratio plot (VESA-GRAM); the mean of the ratio plot was designated the VESA coefficient. The range of variation for these measurements was determined for normal subjects. An application of the technique to patients with hemianopia showed abnormal VESA (characterized by smaller spectral amplitudes over the appropriate hemisphere), abnormal VESA ratio plots, and high VESA coefficients. These preliminary findings suggest that VESA may be a promising method to detect retrochiasmatic visual defects.

A neural network-based spike discriminator.

A software routine to reconstruct individual spike trains from multi-neuron, single-channel extracellular recordings was designed. Using a neural network algorithm that automatically clusters and sorts the spikes, the only user input needed is the threshold level for spike detection and the number of unit types present in the recording. Adaptive features are included in the algorithm to allow for tracking of spike trains during periods of amplitude variation and also to identify noise spikes. The routine will operate on-line during extracellular studies of the cochlear nucleus in cats.

Temporal coding of 200% amplitude modulated signals in the ventral cochlear nucleus of cat.

The quasiperiodicity in the acoustic waveform in speech and music is a pervasive feature in our acoustic environment. The use of 200% amplitude modulated (AM) signals allows the study of rate and temporal envelope coding using three equal amplitude components, a situation that is frequently approximated in natural vocalizations. The recordings reported here were made in the ventral cochlear nucleus of the cat, a site of auditory signal feature enhancement and the origin of several ascending auditory pathways. The discharge rate vs modulation frequency relation was nearly always all-pass in shape for all unit types indicating that discharge rate is not a code for modulation frequency. Onset cells, especially onset-choppers and onset-I units, exhibited remarkable phase locking to the signal envelope, nearly to the exclusion of phase locking to the AM components. They exhibited lowpass temporal modulation transfer functions (tMTF) that occasionally had corner frequencies greater than 1 kHz. Primary-like, primary-like with notch, and onset-L units all exhibited considerable variability in their coding properties with tMTFs that varied from lowpass to bandpass in shape. The bandpass shape became more frequent with increasing stimulus levels. A common feature in cochlear nucleus units was less sensitivity to the level of the AM stimulus than is present in the auditory nerve. Phase locking to the envelope persisted over a wider range of stimulus levels than rate changes in a subset of the units studied. The tMTFs for a 100% sinusoidally modulated, spectrally-flat noise was similar in amplitude and bandwidth to those obtained for AM stimuli. The tMTF was relatively insensitive to carrier frequencies different than the unit characteristic frequency. AM synchrony vs level curves exhibited systematic shifts that equaled or exceeded dynamic rate shifts that occur with increasing levels of a noise masker. Phase locking to the envelope was robust under a wide variety of signal conditions in all unit types. The ordering of response types based on the maximum of the tMTF is onset-I = onset-chop > choppers = primarylike-with-notch = onset-L > primarylike.

Neural encoding of single-formant stimuli in the ventral cochlear nucleus of the chinchilla.

Responses of the principal unit types in the ventral cochlear nucleus of the chinchilla were studied with a single-formant stimulus set that covered fundamental frequency (f0) from 100 Hz to 200 Hz and formant center frequency (F1) from 256 to 782 Hz. Temporal coding for f0 and F1 was explored for 95 stimulus combinations of f0 (n = 5) and F1 (n = 19) in primarylike, onset and chopper unit categories. Several analyses that explored temporal coding were employed including: autocorrelation, interspike interval analysis, and synchronization to each harmonic of f0. In general, the representation of f0 is better in onset and chopper units than in primarylike units. Nearly all units in the cochlear nucleus showed a gain in phase locking to the envelope (f0) of the single-formant stimulus relative to the auditory nerve. The fundamental is represented directly in neural discharges of units in the cochlear nucleus with an interval code (also Cariani and Delgutte, 1996; Rhode, 1995). The formant is represented in the temporal domain in primarylike units, though some chopper and onset units also possess the ability to code F1 through discharge synchrony. Onset-I units, which are associated with the octopus cells, exhibited the strongest phase locking to f0 of any unit types studied. The representation of f0 and F1 in the temporal domain is weak or absent in some units. All-order-interspike interval distributions computed for populations of units show preservation of temporal coding for both f0 and F1. Results are in agreement with earlier amplitude modulation studies that showed nearly all cochlear nucleus unit types phase lock to the signal envelope better than auditory nerve fibers over a considerable range of signal amplitudes.

Two-tone suppression and distortion production on the basilar membrane in the hook region of cat and guinea pig cochleae.

Two-tone suppression and two-tone distortion were investigated at the level of the basilar membrane in the hook region of cat and guinea pig cochleae using a displacement-sensitive laser interferometric measurement system. The system allowed measurements to be performed at physiological stimulus levels in the cochlear region tuned to 30-35 kHz in cat and 29 kHz in guinea pig. The amplitude of vibration of the basilar membrane due to a probe tone at the characteristic frequency (CF) was attenuated during the presentation of a simultaneous suppressor tone either above or below CF. The amount of suppression depended on the intensities of both probe and suppressor, and the relationship of the suppressor frequency to the CF. Suppressors at frequencies more than an octave below the CF attenuated the responses to the CF probe at a rate of up to 1 dB/dB, with little variation based on suppressor frequency. As the suppressor frequency was increased above CF the rate of suppression decreased rapidly. The lowest suppressor intensity at which attenuation of the probe response was observed did not vary in direct proportion to the probe intensity. This suppression threshold often varied only a few dB SPL when the probe was varied over a 20 dB SPL range. In a few instances the rate of attenuation was as much as a factor of two greater at the lowest probe intensities than at higher intensities. It is noteworthy that suppression was found when the frequency of the suppressor was either above or below CF in the same preparation. Low frequency suppressor tones suppress basilar membrane motion at the CF when the basilar membrane undergoes displacement toward either scala. The maximum suppression occurs around 100 microseconds after the peak excursions caused by the low frequency biasing tone. Two-tone distortion products were often observed even at stimulus levels below those causing two-tone suppression at the site studied. The cubic difference tone (CDT) was the most prominent of the distortion products. The level of the CDT component varied nonmonotonically with the level of either of the primary tones. Responses at the difference frequency between the two primaries were usually below the noise floor of the recording system. The existence of both two-tone distortion and two-tone suppression was dependent on the presence of a cochlear nonlinearity.

Basilar membrane mechanics in the hook region of cat and guinea-pig cochleae: sharp tuning and nonlinearity in the absence of baseline position shifts.

A heterodyne laser interferometer was used to observe the movements of small (approximately 20 microns) stainless-steel beads placed on the basilar membrane in the hook region of cat and guinea-pig cochleae. In several preparations, the displacement patterns observed exhibited sharp nonlinear tuning; in one cat this tuning was comparable to that commonly observed in single auditory-nerve fibers. The most sensitive frequencies of the preparations ranged from 31-40 kHz in the cat, and 28-32 kHz in the guinea-pig. The sharp tuning and nonlinearity of the basilar membrane responses was not apparent in surgically or acoustically traumatized preparations. The response nonlinearities were susceptible to temporary threshold shifts and disappeared within a few minutes post-mortem. Stimulus-related shifts in the baseline position of the basilar membrane were not apparent at low stimulus levels. Such shifts were occasionally observed at higher stimulus levels (e.g., > 90 dB SPL), but never approached the fundamental (oscillatory) component of basilar membrane vibration in magnitude. These findings are discussed in relation to previous observations by other workers.

Basilar membrane tonotopicity in the hook region of the cat cochlea.

Middle-ear to basilar membrane (BM) velocity transfer functions are reported for seven locations in the hook region of a single cat cochlea. These transfer functions were recorded at high sound pressure levels in a linearized, or passive cochlea, and resemble those reported previously by Wilson and Evans (1983). They demonstrate longitudinal tonotopicity with a gradient of approximately 3.6 mm/octave. When allowances are made for the nonlinear mechanisms previously demonstrated in active hook region preparations (Cooper and Rhode, 1992), the data are also consistent with the tonotopic map derived from the intracellular dye-filling studies of Liberman (1982).

Representation of vowel stimuli in the ventral cochlear nucleus of the chinchilla.

Responses of neurons in the ventral cochlear nucleus (VCN) of anesthetized chinchillas to six synthetic vowel sounds (/a/, /e/, /epsilon/, /i/, /o/ and /u/) were recorded at several intensity levels. Stimuli were synthesized with a fundamental frequency of 100 Hz or 181.6 Hz and had formant values at integer multiples of 100 Hz. Responses came from most neuron types in the VCN (with the exception of onset cells with an I-shaped pattern). Population studies, performed only on primary-like (PL) and chopper neurons, showed that PL neurons provide a better temporal representation than do chopper neurons. At the lowest level of stimulation, all neuron types provide an accurate rate-place representation of vowel spectra. With an increase in stimulus level, the rate-place representation of PL neurons becomes inferior to that of chopper neurons, either sustained choppers or transient choppers.

Nonlinear mechanics at the apex of the guinea-pig cochlea.

A heterodyne laser interferometer was used to observe the sound-evoked displacement patterns of Reissner's membrane and various other structures in the apical turn of the guinea-pig cochlea. Most structures (including the basilar membrane) were similarly tuned, and had best frequencies in the 200-350Hz range. A distinct notch was usually observed approximately 0.7 octaves above the best frequency, and amplitude- and phase-plateaus were observed at higher frequencies. In most other respects, however, the mechanical tuning resembled the frequency-threshold curves of low frequency cochlear nerve fibers. In five reasonably intact, in vivo preparations, the frequency of the mechanical sensitivity notch was intensity-dependent: Compressive nonlinearities were observed above approximately 80 dB SPL on the low-frequency side of the notch, with antagonistically expansive nonlinearities on the high-frequency side. Two-tone suppression was observed in one of these preparations. Stimulus-related baseline position shifts were observed in another in vivo preparation. No such nonlinearities were observed in structurally damaged and/or > 1 hour post-mortem preparations. However, more robust nonlinearities were observed in all preparations at higher levels of stimulation (e.g. > 100-110 dB SPL). These high-level nonlinearities diminished only slowly after death, and gave rise to various effects, including time-dependent (i.e. adapting) and severely distorted (e.g. peak-split and/or dc-shifted) responses.

Characteristics of tone-pip response patterns in relationship to spontaneous rate in cat auditory nerve fibers.

The responses of single auditory nerve (AN) fibers in the cat were recorded in response to 25 ms tone pips. Peristimulus time histograms (PSTH) of discharge patterns recorded from fibers with high spontaneous rates (high SRs), show that the discharge rate rapidly adapts to a much lower steady-state level over a 15 ms period with shorter times for units with best frequencies (CFs) greater than 5 kHz. The PSTHs of auditory nerve fibers with low SRs do not show this pattern of rapid adaptation. Differences between the high and low SR populations include higher thresholds, better tuning, and longer latency in the low SR population. The peak-to-steady-state discharge ratio is an increasing function of SR and CF; it varies from 1.0 for fibers with SR = 0 to over 8 for fibers with high SRs and CFs near 10 kHz. This ratio increases with increasing stimulus intensity and stimulus recovery time. The high SR population shows a number of responses to transients which are weak or absent in the low SR population. Increasing the recovery time shortened the latency of both high and low SR AN fibers by as much as 1 ms. A number of other response properties of AN fibers are also reported that are important when interpreting the responses of cochlear nucleus neurons to tone pips.

Cosmic ray electrons and positrons from supernova explosions of massive stars.

We attribute the recently discovered cosmic ray electron and cosmic ray positron excess components and their cutoffs to the acceleration in the supernova shock in the polar cap of exploding Wolf-Rayet and red supergiant stars. Considering a spherical surface at some radius around such a star, the magnetic field is radial in the polar cap as opposed to most of 4pi (the full solid angle), where the magnetic field is nearly tangential. This difference yields a flatter spectrum, and also an enhanced positron injection for the cosmic rays accelerated in the polar cap. This reasoning naturally explains the observations. Precise spectral measurements will be the test, as this predicts a simple E;{-2} spectrum for the new components in the source, steepened to E;{-3} in observations with an E;{-4} cutoff.