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The probability that a cochlear nerve fiber spike discharge occurs during a time interval delta t depends on both the acoustic stimulus and on aftereffects from earlier spike discharges. We have examined the influence of discharge-history on post-stimulus time (PST) histogram responses to acoustic click and tone-burst stimuli. Discharge-history effects were found to include the modification of observed interpeak times of PST responses to clicks, a loss of distinct peaks in the click response of high characteristic frequency (CF greater than 5 kHz) fibers, and changes in the ratio of initial to steady-state response portions of tone-burst responses. The method used to separate discharge-history from stimulus-related factors is based on a model developed in Gaumond et al. [J. Neurophysiol. 48, 856-873 (1982)]. The results are in general agreement with those obtained by the method of Peter Gray [Biophys. J. 7, 759-777 (1967)], which discards from consideration those portions of the response record not preceded by a silent interval of 20 or 25 ms or more. Our method requires more assumptions about the spike train, but produces less variable results by utilizing more of the spike train data.

Five polyphosphazenes with different hydrophilicites were synthesized and screened in vitro. The purpose was to identify unique types of polymeric substrates that distinctly favored or markedly prevented cellular adhesion. The SK-N-BE(2c) human neuroblastoma cell line, utilized for its electrogenic responses, was used to test this differential adhesion. In particular, the objective was to specifically culture this cell line in a highly selective pattern. Each candidate polymer was cast into films and plated with neuroblastoma cells for 3 days. The polyphosphazene materials which showed negative cellular adhesive properties (-CAPs) were poly[bis(trifluoroethoxy)phosphazene] (TFE) and poly[bis(methoxyethoxyethoxy)phosphazene] (MEEP). The polyphosphazenes which showed positive cellular adhesive properties (+CAPs) were poly[(methoxyethoxyethoxy)(1.0)(carboxylatophenoxy)(1.0)phosphazene] (PMCPP), poly[(methoxyethoxyethoxy)(1.0)(cinnamyloxy)(1.0)phosphazene] (PMCP), and poly[(methoxyethoxyethoxy)(1.0)(p-methylphenoxy)(1.0)phosphazene] (PMMP). To test cellular selectivity, films of -CAP and +CAP were copatterned onto glass substrates. The micropatterned films were plated with SK-N-BE(2c) neuroblastoma cells for one week. The results showed that neuroblastoma cells adhere selectively (over 60%) to the +CAP microfeatures. We also showed that multiple properties can be achieved with a single material and that we can use TFE as both a -CAP and an insulation layer and PMCP as a conductive +CAP layer.

Two simple models are examined in order to explain the observation that a portion of the binaural-evoked response is less than the sum of monaural-evoked responses in human and animal subjects. The sum of monaural responses minus the binaural response is called the binaural difference (BD). Each model acts on binaural input signals and applies a single memoryless nonlinearity. One model (IE) applies a rectifying nonlinearity to the difference of input signals, while the other (EE) applies a compressive nonlinearity to the sum of input signals. These models are suggested by properties of inhibitory-excitatory (IE) and excitatory-excitatory (EE) neurons of the auditory brainstem. Parameters can be found that enable each model to produce a ratio of BD to summed monaural response which is invariant with input stimulus level. The IE model, but not the EE model, has a BD whose level is linearly related to input stimulus level.

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