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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.

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.

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.