scholarly journals Topography of Interaural Temporal Disparity Coding in Projections of Medial Superior Olive to Inferior Colliculus

2003 ◽  
Vol 23 (19) ◽  
pp. 7438-7449 ◽  
Author(s):  
Douglas L. Oliver ◽  
Gretchen E. Beckius ◽  
Deborah C. Bishop ◽  
William C. Loftus ◽  
Ranjan Batra
1995 ◽  
Vol 88 (1-2) ◽  
pp. 71-78 ◽  
Author(s):  
Shigeo Okoyama ◽  
Tetsuji Moriizumi ◽  
Yasuko Kitao ◽  
June Kawano ◽  
Motoi Kudo

1985 ◽  
Vol 53 (1) ◽  
pp. 89-109 ◽  
Author(s):  
G. Harnischfeger ◽  
G. Neuweiler ◽  
P. Schlegel

Single-unit responses to tonal stimulation with interaural disparities were recorded in the nuclei of the superior olivary complex (SOC) and the central nucleus of the inferior colliculus (ICC) of the echolocating bat, Molossus ater. Seventy-six units were recorded from the ICC and 74 from the SOC; of the SOC units, 31 were histologically verified in the medial superior olive (MSO), 10 in the lateral superior olive (LSO), and 33 in unidentified areas of the SOC. Best frequencies (BFs) of the units ranged from 10.3 to 89.6 kHz, and Q10 dB values ranged from 2 to 70 dB. Most ICC neurons responded phasically to stimulus onset and were either inhibitory/excitatory [I/E; (53)] or excitatory/excitatory [E/E; (21)] units. In the MSO, 23 units responded tonically and 7 phasically on, 18 were E/E or E/OF (facilitatory for other input) units, and 11 were I/E neurons. All LSO neurons responded in a "chopper" fashion, and the binaural neurons were E/I units. In E/E units the excitatory response to binaural stimulation was frequently larger than the sum of the monaurally evoked responses. Many neurons with E/I or I/E inputs had very steep binaural impulse-count functions and were sensitive to small interaural intensity differences. Twenty-eight units (24%) responded with a change in firing rate of at least 20% to interaural time differences of +/- 500 microseconds. Within this sample, 11 units (8 from ICC, 2 from MSO, and 1 from SOC) were sensitive to interaural time differences of only +/- 50 microseconds. Of these 11 units, 10 were I/E units responding phasically only to stimulus onset and were also sensitive to intensity differences (delta I), being suppressed completely by the inhibitory input over a delta I range of 20 dB or less. Of 117 units tested in the ICC and SOC nuclei, 86 units (76%) were not sensitive to interaural time disparities within +/- 500 microseconds. Because the BFs of these units sensitive to interaural transient time differences (delta t) ranged between 18 and 90 kHz, responses were elicited by pure tones, and responses did not change periodically with the period equal to that of the stimulus frequency, we conclude that the neurons reacted to interaural differences of stimulus-onset time (transient time difference) but not to phase differences (ongoing time difference). Sensitivity to interaural time differences was also correlated with interaural intensity differences.(ABSTRACT TRUNCATED AT 400 WORDS)


2002 ◽  
Vol 88 (5) ◽  
pp. 2251-2261 ◽  
Author(s):  
Ramnarayan Ramachandran ◽  
Bradford J. May

Decerebration allows single-unit responses in the central nucleus of the inferior colliculus (ICC) to be studied in the absence of anesthesia and descending efferent influences. When this procedure is applied to cats, three neural response types (V, I, and O) can be identified by distinct patterns of excitation and inhibition in pure-tone frequency-response maps. Similarities of the definitive response map features with those of projection neurons in the auditory brain stem have led to the proposal that the ICC response types are derived from different sources of ascending input that remain functionally segregated within the midbrain. Additional evidence for the existence of these hypothesized parallel processing pathways has been obtained in our previous investigations of the effects of interaural level differences, brain stem lesions, and pharmacological manipulations on physiologically classified units. This study extends our characterization of the functional segregation of single-unit activity in the ICC by investigating how sensitivity to interaural time differences (ITDs) is related to the response types that are observed in decerebrate cats. The results of these experiments support our parallel-processing model of the ICC by linking the ITD sensitivity of type V and I units to putative inputs from the medial superior olive and lateral superior olive and by showing that most type O units lack a systematic sensitivity to binaural temporal information presumably because their dominant ascending inputs arise from weakly binaural neurons in the dorsal cochlear nucleus.


1995 ◽  
Vol 88 (1-2) ◽  
pp. 65-70 ◽  
Author(s):  
Shigeo Okoyama ◽  
Tetsuji Moriizumi ◽  
Yasuko Kitao ◽  
June Kawano ◽  
Motoi Kudo

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