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The superior olivary complex is a group of brainstem nuclei involved in hearing and includes the medial superior olive (MSO) and the lateral superior olive (LSO), surrounded by periolivary cell groups. The structure and functional roles of the MSO and LSO have been the subject of many investigations in laboratory animals and it has largely been assumed that these findings are directly transferable to humans. However, little is known conclusively regarding the detailed organization of the human superior olivary complex. The goal of this study is to provide a detailed analysis of the cytoarchitecture of the human MSO and LSO. Results from the examination of eight human brainstems confirm the existence of a conserved MSO and provide evidence of a prominent and highly ordered LSO. Unbiased stereological estimates of neuronal number indicate approximately 15,500 neurons in the MSO and 5600 neurons in the LSO. Additionally, a three-dimensional model of the MSO and LSO was constructed and provides evidence that the human LSO is composed of medial and lateral segments. Finally, an analysis of neuronal morphology, in Nissl stained and Golgi impregnated tissue, provides evidence of multiple neuronal classes within each nucleus and further that these neurons demonstrate a precise geometric arrangement (depending on the nucleus) that is suggestive of isofrequency laminae.

Data from humans and animal models provide evidence for an age-dependent impairment in the ability to localize sound. The lateral superior olive (LSO) in the ascending auditory pathway is one important center involved in processing of binaural auditory stimuli. To identify potential age-dependent changes we characterized the LSO in young (15 months) and old (or =3 years) gerbils with a special emphasis on the expression of GABA- and glycine-like immuno-reactivity. The dimensions of the LSO, as well as the number and density of glycine- and GABA-immuno-reactive neurons, were not significantly different between young and old gerbils. The size of glycine- and GABA-immuno-reactive neurons was significantly reduced in the high-frequency (medial) limb of the LSO. Over all, age-dependent changes in the LSO of the gerbil were small.

Lateral superior olive (LSO) neurons in young and aged Sprague-Dawley rats have functional properties consistent with a limited contralateral inhibition, which is markedly different from other animals. An unusually low proportion of LSO cells (36/113) exhibited contralateral inhibition (and ipsilateral excitation, IE), while over 25% of LSO units exhibited excitatory responses to contralateral stimuli. Inhibition of most IE LSO neurons was evident only when the contralateral intensity was greater than the ipsilateral intensity, resulting in a marked shift in sensitivity to interaural intensity differences (IID). The firing rate of IE neurons was also affected more by a change in intensity of ipsilateral compared to contralateral stimuli. The shift in the IID sensitivity and the relative decrease in effectiveness of contralaterally driven inhibition in Sprague-Dawley rat LSO neurons could be due to decreased inhibitory inputs from the MNTB principal cells, increased contralateral excitatory effects and/or increased ipsilateral excitatory effects. Age-related decreases in the numbers of MNTB neurons observed anatomically is not reflected in a change in LSO function. The Sprague-Dawley rat may be a useful model for the effect of reduced inhibition in the superior olivary complex on auditory behavior.

Short-term adaptation was examined in single unit recordings from 113 superior olive neurons of anaesthetized 3- to 6-month-old Long-Evans rats. Responses to an equal intensity BF probe tone presented 1 ms after an 'adapting' BF tone were adapted by 56.3 +/- 2.6% (mean +/- S.E.) compared to responses at a 512 ms delay. The rapid decrease in discharge rate during adapting tones often approximated exponential time courses with time constants of less than 20 ms. The recovery from adaptation was exponential with time constants of 106 +/- 20.0 ms. The magnitude of adaptation and time course of recovery following monaural stimulation of binaurally excited (EE) neurons were not significantly different in both input pathways. Additionally, in 60% of EE neurons, an 'adapting' tone presented to one ear reduced subsequent responses to probe tones presented to the opposite ear. Binaural stimulation resulted in equal or greater adaptation of responses than monaural stimulation of either ear. The recovery of binaural excitatory responses generally followed a time course between recovery functions for ipsilateral and contralateral monaural stimuli. Lateral Superior Olive (LSO) neurons encode sound source location through the interaction of ipsilateral excitation and contralateral inhibition (IE). Ipsilaterally driven excitatory responses in LSO neurons exhibited the greatest magnitude of adaptation (68.5 +/- 21.1%). Adaptation of inhibition was observed in over half of IE neurons. Responses of LSO neurons to binaural BF probe stimuli were greatest immediately after a 200 ms BF 'inhibitory adapting' stimulus to the contralateral ear, and decreased with greater interstimulus delays. Responses to binaural stimulation were constant after prior binaural adaptation, when the magnitude and recovery of adaptation to monaural stimuli were similar for excitation and inhibition (8/25 IE cells). The functional significance and possible sites of adaptation processes are discussed.

A general point process theory is developed to describe discharges recorded from lateral superior olivary units of the cat responding to ipsilaterally presented tone bursts and continuous tones. Statistical analysis of the stationary portion of the sequence of interspike intervals demonstrated that, for most units, the duration of each interval is statistically dependent only on the duration of the previous interval. A specific point process model is derived based on this analysis to describe the measured serial dependence as well as the deadtimes observed in interval histograms. The statistical dependence is well described as a shift of the interspike interval distribution, the shift depending on the duration of the previous interval. This model is then used to simulate the initial chopping in the tone burst responses. It is concluded that chopping responses and serial dependence do not result from properties of the unit's inputs; rather, they are consequences of the inherent characteristics of the unit.

Superposition of point processes has often been suggested as an abstract model for the generation of neural discharge patterns due to its simplicity (input spike trains are simply merged and then retransmitted by the model neuron). The properties of the superposition of two renewal processes are examined in relation to the properties of its components. A satisfactory condition is found so that the superposition of two renewal processes possesses negative serial dependence of interevent intervals. However, the imposition of a dead time of approximately the same duration as that of the components on their superposition process is shown to remove much of this dependence. Thus, the adequacy of the simple superposition of renewal processes as a model for discharge patterns from regions that are typified by negative serial dependence (such as the lateral superior olive) may be limited, but may suffice for the discharges of primary-like units.