@inproceedings {Palanca-Castan1799_2016, year = {2016}, author = {Palanca-Castan, Nicolas and Laumen, Geneviève and Reed, Darrin and Köppl, Christine}, title = {Characterization of the Binaural Interaction Component in Barn Owl (Tyto alba)}, booktitle = {Assoc. Res. Otolaryng. MidWinter Meeting (ARO)}, URL = {http://c.ymcdn.com/sites/www.aro.org/resource/resmgr/Abstract_Archives/UPDATED_2016_ARO_Abstract_Bo.pdf}, abstract = {Background The auditory brainstem response (ABR) is an evoked potential that reflects the responses to sound by the brainstem neural centers. The binaural interaction component (BIC) is obtained by subtracting the sum of the monaural ABR responses from the binaural response. It is assumed to represent the activity of binaural nuclei (Jewett, 1970, Electroencephalogr. Clin. Neurophysiol. 28: 609–618). The amplitude and latency of the BIC are dependent on the binaural cues presented (Furst et al., 1990, Hear. Res. 187: 63–72). The BIC can be used to non-invasively test binaural processing. However, any conclusions are limited by the lack of knowledge of the relevant processes at the level of individual neurons. The aim of this study is to characterize the ABR and BIC in the barn owl, an animal where the ITD-processing neural circuits have been extensively studied. Methods ABRs were measured in 9 adult barn owls. Responses to chirps at different levels and ITDs were recorded, and the BIC was derived as a function of ITD. To determine the extent of the crosstalk caused by the presence of the interaural canal, compound action potential (CAP) recordings were collected for two other adult barn owls. All BIC measurements were taken below the level of crosstalk. Results The ABR in barn owl showed 2-3 waves in the first 10 ms of recording. Wave I only appeared consistently at high levels. Wave II and III increased in amplitude and decreased in latency with increasing stimulus level. The most salient component of the BIC was a negative deflection (DN1) that corresponded to wave III. The latency of DN1 closely corresponded to the latency of local neurophonic potentials recorded in nucleus laminaris (Carr et al. 2015, J. Neurophysiol., in press). Both the amplitude and latency of DN1 varied with changing ITD. Conclusion The most visible component of the BIC (DN1) was associated with nucleus laminaris and is thus likely to reflect the known processes of ITD computation in this nucleus. DN1 was a negative deflection, which indicates a smaller response to binaural stimulation than predicted by the sum of monaural responses. This negative polarity is not consistent with previous predictions (Wada and Starr, 1989, Electroencephalogr. Clin. Neurophysiol. 56, 340–351) for an excitatory-excitatory system such as the one present in barn owl, and alternative models like the one by Gaumond and Psaltikidou (1991, J. Acoust. Soc. Am. 89: 454:456) need to be considered. Funding NPC, GL, CK funded by the DFG (TRR31) and the cluster of excellent “Hearing4all”. DK supported by the program “Function and pathophysiology of the auditory system” funded by the state of Lower Saxony, Germany.} }