The representation of steady‐state vowel sounds in the temporal discharge patterns of the guinea pig cochlear nerve and primarylike cochlear nucleus neurons

1986 ◽  
Vol 79 (1) ◽  
pp. 100-113 ◽  
Author(s):  
A. R. Palmer ◽  
I. M. Winter ◽  
C. J. Darwin
1990 ◽  
Vol 63 (5) ◽  
pp. 1191-1212 ◽  
Author(s):  
C. C. Blackburn ◽  
M. B. Sachs

1. We have recorded the responses of neurons in the anteroventral cochlear nucleus (AVCN) of barbiturate-anesthetized cats to the synthetic, steady-state-vowel sound /e/, presented over a range of stimulus intensities. 2. The responses of (putative) spherical bushy cells [primary-like (Pri) units] to the vowel resemble those of auditory-nerve fibers (ANFs) in terms of both rate and temporal encoding at low and moderate stimulus levels. It was not possible to study the responses of most Pri units at the highest stimulus level because of the large neurophonic component present in recordings from most primarylike units at higher stimulus levels. 3. The responses of many (putative) globular bushy cells [primarylike with notch (PN) units] to the vowel resemble those of ANFs; however, there appears to be greater heterogeneity in the responses of units in the PN population than in the Pri population in terms of both temporal and rate encoding. 4. Populations of stellate cells (chopper units) have degraded representations of the temporal information in ANF population discharge patterns in response to the vowel; this is consistent with the responses of these units to pure tones. Both regular (ChS) and irregular (ChT) chopper subpopulations, however, maintain better rate-place representations of the vowel spectrum than does the population of ANFs as a whole. The rate-place representations of the vowel spectrum by both chopper populations closely resemble those of low and medium spontaneous rate ANFs at most stimulus levels. 5. The data presented in this paper suggest that a functional partition of the AVCN chopper population could yield two distinct rate representations in response to a complex stimulus: one that is graded with stimulus level (over a 30 to 40 dB range) and that, even at rate saturation, maintains a "low contrast" stimulus representation; and a second that maintains a robust, "high contrast" stimulus representation at all levels but that confers less information about stimulus level.


1990 ◽  
Vol 63 (2) ◽  
pp. 333-346 ◽  
Author(s):  
R. Nitzan ◽  
I. Segev ◽  
Y. Yarom

1. Intracellular recordings from neurons in the dorsal motor nucleus of the vagus (vagal motoneurons, VMs) obtained in the guinea pig brain stem slice preparation were used for both horseradish peroxidase (HRP) labeling of the neurons and for measurements of their input resistance (RN) and time constant (tau 0). Based on the physiological data and on the morphological reconstruction of the labeled cells, detailed steady-state and compartmental models of VM were built and utilized to estimate the range of membrane resistivity, membrane capacitance, and cytoplasm resistivity values (Rm, Cm, and Ri, respectively) and to explore the integrative properties of these cells. 2. VMs are relatively small cells with a simple dendritic structure. Each cell has an average of 5.3 smooth (nonspiny), short (251 microns) dendrites with a low order (2) of branching. The average soma-dendritic surface area of VMs is 9,876 microns 2. 3. Electrically, VMs show remarkably linear membrane properties in the hyperpolarizing direction; they have an average RN of 67 +/- 23 (SD) M omega and a tau 0 of 9.4 +/- 4.1 ms. Several unfavorable experimental conditions precluded the possibility of faithfully recovering ("peeling") the first equalizing time constant (tau 1) and, thereby, of estimating the electrotonic length (Lpeel) of VMs. 4. Reconciling VM morphology with the measured RN and tau 0 through the models, assuming an Ri of 70 omega.cm and a spatially uniform Rm, yielded an Rm estimate of 5,250 omega.cm2 and a Cm of 1.8 microF/cm2. Peeling theoretical transients produced by these models result in an Lpeel of 1.35. Because of marked differences in the length of dendrites within a single cell, this value is larger than the maximal cable length of the dendrites and is twice as long as their average cable length. 5. The morphological and physiological data could be matched indistinguishably well if a possible soma shunt (i.e., Rm, soma less than Rm, dend) was included in the model. Although there is no unique solution for the exact model Rm, a general conclusion regarding the integrative capabilities of VM could be drawn. As long as the model is consistent with the experimental data, the average input resistance at the dendritic terminals (RT) and the steady-state central (AFT----S) and peripheral (AFS----T) attenuation factors are essentially the same in the different models. With Ri = 70 omega.cm, we calculated RT, AFS----T, and AFT----S to be, on the average, 580 M omega, 1.1, and 13, respectively.(ABSTRACT TRUNCATED AT 400 WORDS)


2003 ◽  
Vol 89 (6) ◽  
pp. 3097-3113 ◽  
Author(s):  
Jason S. Rothman ◽  
Paul B. Manis

Using kinetic data from three different K+ currents in acutely isolated neurons, a single electrical compartment representing the soma of a ventral cochlear nucleus (VCN) neuron was created. The K+ currents include a fast transient current ( IA), a slow-inactivating low-threshold current ( ILT), and a noninactivating high-threshold current ( IHT). The model also includes a fast-inactivating Na+ current, a hyperpolarization-activated cation current ( Ih), and 1–50 auditory nerve synapses. With this model, the role IA, ILT, and IHT play in shaping the discharge patterns of VCN cells is explored. Simulation results indicate that IHT mainly functions to repolarize the membrane during an action potential, and IA functions to modulate the rate of repetitive firing. ILT is found to be responsible for the phasic discharge pattern observed in Type II cells (bushy cells). However, by adjusting the strength of ILT, both phasic and regular discharge patterns are observed, demonstrating that a critical level of ILT is necessary to produce the Type II response. Simulated Type II cells have a significantly faster membrane time constant in comparison to Type I cells (stellate cells) and are therefore better suited to preserve temporal information in their auditory nerve inputs by acting as precise coincidence detectors and having a short refractory period. Finally, we demonstrate that modulation of Ih, which changes the resting membrane potential, is a more effective means of modulating the activation level of ILT than simply modulating ILT itself. This result may explain why ILT and Ih are often coexpressed throughout the nervous system.


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