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The Journal of Neurophysiology Vol. 87 No. 2 February 2002, pp. 976-994
Copyright ©2002 by the American Physiological Society
1Eaton-Peabody Laboratory, Massachusetts Eye and Ear Infirmary, Boston 02143; 2Hearing Research Center, Boston University, Boston 02215; and 3Research Laboratory of Electronics, MIT, Cambridge, Massachusetts 02114
Litovsky, R. Y. and
B. Delgutte.
Neural Correlates of the Precedence Effect in the Inferior
Colliculus: Effect of Localization Cues. J. Neurophysiol. 87: 976-994, 2002. The precedence effect (PE) is an
auditory phenomenon involved in suppressing the perception of echoes in
reverberant environments, and is thought to facilitate accurate
localization of sound sources. We investigated physiological correlates
of the PE in the inferior colliculus (IC) of anesthetized cats, with a
focus on directional mechanisms for this phenomenon. We used a virtual
space (VS) technique, where two clicks (a "lead" and a "lag")
separated by a brief time delay were each filtered through head-related
transfer functions (HRTFs). For nearly all neurons, the response to the
lag was suppressed for short delays and recovered at long delays. In
general, both the time course and the directional patterns of
suppression resembled those reported in free-field studies in many
respects, suggesting that our VS simulation contained the essential
cues for studying PE phenomena. The relationship between the
directionality of the response to the lead and that of its suppressive
effect on the lag varied a great deal among IC neurons. For a majority
of units, both excitation produced by the lead and suppression of the
lag response were highly directional, and the two were similar to one
another. For these neurons, the long-lasting inhibitory inputs thought
to be responsible for suppression seem to have similar spatial tuning
as the inputs that determine the excitatory response to the lead.
Further, the behavior of these neurons is consistent with
psychophysical observations that the PE is strongest when the lead and
the lag originate from neighboring spatial locations. For other
neurons, either there was no obvious relationship between the
directionality of the excitatory lead response and the directionality of suppression, or the suppression was highly directional whereas the
excitation was not, or vice versa. For these neurons, the excitation
and the suppression produced by the lead seem to depend on different
mechanisms. Manipulation of the directional cues (such as interaural
time and level differences) contained in the lead revealed further
dissociations between excitation and suppression. Specifically, for
about one-third of the neurons, suppression depended on different
directional cues than did the response to the lead, even though the
directionality of suppression was similar to that of the lead response
when all cues were present. This finding suggests that the inhibitory
inputs causing suppression may originate in part from subcollicular
auditory nuclei processing different directional cues than the inputs
that determine the excitatory response to the lead. Neurons showing
such dissociations may play an important role in the PE when the lead
and the lag originate from very different directions.
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