Marginal shell of the anteroventral cochlear nucleus: Single-unit response properties in the unanesthetized decerebrate cat. S. Ghoshal and D. O. Kim. Division Otolaryngology, Surgical Research Center, Department of Surgery, Neuroscience Program, Biomedical Engineering Program, University of Connecticut Health Center, Farmington, CT 06030-1110, USA.
APStracts 4:0014N, 1997.
ABSTRACT
The marginal shell of the anteroventral cochlear nucleus (AVCN) is anatomically different from its central core. We investigated 38 single units in the shell of 10 cats and contrasted them with 62 single units in the core of 15 cats. The sites of all shell units were localized using reconstructed electrode tracks. The shell units were divided into acoustically well-driven (68%) and weakly/not-driven (32%) subgroups. The shell units mostly exhibited low spontaneous rates (SR). Among the well-driven shell units, a large majority (68%) exhibited wide dynamic ranges (ò 50 dB) to tones, noise or both, with some as wide as 89 dB. In contrast, a large majority (80%) of the core units exhibited narrow dynamic ranges (< 50 dB) to tones and noise. The post-stim ulus time histograms (PSTHs) of the well-driven shell units included pause-build (29%), onset (24%) and unusual (33%) types while those of the core units were mainly primarylike (47%) and chopper (29%) types. The excitatory- inhibitory areas (EIAs) of the well-driven shell units included types I/III (47%), III (22%), IV (13%) and II (9%) while those of the core units were mainly types III (52%) and I/III (32%). Based on Fisher's exact tests, we conclude that the shell and core neural groups of the AVCN are significantly different regarding all of the following physiological characteristics: SR, maximum driven rate, threshold and dynamic range to tones and noise, frequency response area, PSTH type, latency, and EIA types. Wide dynamic ranges of the well-driven shell units suggest that they may play a role in encoding absolute intensity of acoustic stimulus.

Received 19 June 1996; accepted in final form 13 December 1996.
APS Manuscript Number J487-6.
Article publication pending J. Neurophysiol.
ISSN 1080-4757 Copyright 1997 The American Physiological Society.
Published in APStracts on 21 January 1997