» Articles » PMID: 17699697

Spectral Composition of Concurrent Noise Affects Neuronal Sensitivity to Interaural Time Differences of Tones in the Dorsal Nucleus of the Lateral Lemniscus

Overview
Journal J Neurophysiol
Specialties Neurology
Physiology
Date 2007 Aug 19
PMID 17699697
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

We are regularly exposed to several concurrent sounds, producing a mixture of binaural cues. The neuronal mechanisms underlying the localization of concurrent sounds are not well understood. The major binaural cues for localizing low-frequency sounds in the horizontal plane are interaural time differences (ITDs). Auditory brain stem neurons encode ITDs by firing maximally in response to "favorable" ITDs and weakly or not at all in response to "unfavorable" ITDs. We recorded from ITD-sensitive neurons in the dorsal nucleus of the lateral lemniscus (DNLL) while presenting pure tones at different ITDs embedded in noise. We found that increasing levels of concurrent white noise suppressed the maximal response rate to tones with favorable ITDs and slightly enhanced the response rate to tones with unfavorable ITDs. Nevertheless, most of the neurons maintained ITD sensitivity to tones even for noise intensities equal to that of the tone. Using concurrent noise with a spectral composition in which the neuron's excitatory frequencies are omitted reduced the maximal response similar to that obtained with concurrent white noise. This finding indicates that the decrease of the maximal rate is mediated by suppressive cross-frequency interactions, which we also observed during monaural stimulation with additional white noise. In contrast, the enhancement of the firing rate to tones at unfavorable ITD might be due to early binaural interactions (e.g., at the level of the superior olive). A simple simulation corroborates this interpretation. Taken together, these findings suggest that the spectral composition of a concurrent sound strongly influences the spatial processing of ITD-sensitive DNLL neurons.

Citing Articles

The calyx of Held in the auditory system: Structure, function, and development.

Baydyuk M, Xu J, Wu L Hear Res. 2016; 338:22-31.

PMID: 27018297 PMC: 4967386. DOI: 10.1016/j.heares.2016.03.009.


Circuit models and experimental noise measurements of micropipette amplifiers for extracellular neural recordings from live animals.

Chen C, Pun S, Un Mak P, Vai M, Klug A, Lei T Biomed Res Int. 2014; 2014:135026.

PMID: 25133158 PMC: 4123482. DOI: 10.1155/2014/135026.


Neural encoding of sound source location in the presence of a concurrent, spatially separated source.

Day M, Koka K, Delgutte B J Neurophysiol. 2012; 108(9):2612-28.

PMID: 22914651 PMC: 3545175. DOI: 10.1152/jn.00303.2012.


Age-related dissociation of sensory and decision-based auditory motion processing.

Ludwig A, Rubsamen R, Dorrscheidt G, Kotz S Front Hum Neurosci. 2012; 6:64.

PMID: 22470331 PMC: 3313480. DOI: 10.3389/fnhum.2012.00064.


Adaptation of binaural processing in the adult brainstem induced by ambient noise.

Siveke I, Leibold C, Schiller E, Grothe B J Neurosci. 2012; 32(2):462-73.

PMID: 22238082 PMC: 6621091. DOI: 10.1523/JNEUROSCI.2094-11.2012.