Abstract
Jeffress (J Comp Physiol Psychol 41:35-39, 1948) proposed that external interaural time differences (ITDs) are compensated by internal, axonal delays allowing ITD to be represented by a population of coincidence detectors in the medial superior olive (MSO). The MSO shows a strong extracellular field potential: the neurophonic. Studies in the barn owl reported a phase shift in the neurophonic along the nucleus laminaris and concluded that this phase shift is consistent with axonal delay lines as proposed by Jeffress. We recorded the neurophonic in the MSO of the cat at various locations along its short, dendritic axis. A phase shift of about 0.5 cycles was observed at depths close to the amplitude maxima, sometimes accompanied by localized amplitude minima. Current source density analysis for contralateral (ipsilateral) stimulation shows a current source close to a neurophonic amplitude maximum and a sink 100 μm ventromedially (dorsolaterally). These results indicate that some of the features of the neurophonic may be caused by a dipole field. Contralateral (ipsilateral) excitation causes a current sink at the ventromedial (dorsolateral) dendrites and a source at the soma and dorsolateral (ventromedial) dendrites. The difference in phase at the sink and source is 0.5 cycles, which closely resembles the phase shift that has been reported in the barn owl. Our interpretation in terms of a dipole field raises the question whether the neurophonic phase shift reported in the barn owl reflects axonal delays or simply a nucleus laminaris dipole configuration.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Adams JC, Mugnaini E (1990) Immunocytochemical evidence for inhibitory and disinhibitory circuits in the superior olive. Hear Res 49:281–298
Biedenbach MA, Freeman WJ (1964) Click-evoked potential map from the superior olivary nucleus. Am J Physiol 206:1408–1414
Bojanowski T, Hu K, Schwarz DW (1989) Analogue signal representation in the medial superior olive of the cat. J Otolaryngol 18:3–9
Boudreau JC (1965) Stimulus correlates of wave activity in the superior-olivary complex of the cat. J Acoust Soc Am 37:779–785
Cant NB, Hyson RL (1992) Projections from the lateral nucleus of the trapezoid body to the medial superior olivary nucleus in the gerbil. Hear Res 58:26–34
Carr CE, Konishi M (1990) A circuit for detection of interaural time differences in the brain stem of the barn owl. J Neurosci 10:3227–3246
Freeman JA, Nicholson C (1975) Experimental optimization of current source-density technique for anuran cerebellum. J Neurophysiol 38:369–382
Galambos R, Schwartzkopff J, Rupert A (1959) Microelectrode study of superior olivary nuclei. Am J Physiol 197:527–536
Guinan JJ, Norris BE, Guinan SS (1972) Single auditory units in the superior olivary complex. II: Locations of unit categories and tonotopic organization. Int J Neurosci 4:147–166
Helfert RH, Bonneau JM, Wenthold RJ, Altschuler RA (1989) GABA and glycine immunoreactivity in the guinea pig superior olivary complex. Brain Res 501:269–286
Jeffress LA (1948) A place theory of sound localization. J Comp Physiol Psychol 41:35–39
Joris PX, Carney LHC, Smith PH, Yin TCT (1994) Enhancement of synchronization in the anteroventral cochlear nucleus. I. Responses to tonebursts at characteristic frequency. J Neurophysiol 71:1022–1036
Kapfer C, Seidl AH, Schweizer H, Grothe B (2002) Experience-dependent refinement of inhibitory inputs to auditory coincidence-detector neurons. Nat Neurosci 5:247–253
Koppl C, Carr CE (2008) Maps of interaural time difference in the chicken’s brainstem nucleus laminaris. Biol Cybern 98:541–559
Lorente De Nó R (1947) Action potential of the motoneurons of the hypoglossus nucleus. J Cell Comp Physiol 29:207–287
Manis PB, Brownell WE (1983) Synaptic organization of eighth nerve afferents to cat dorsal cochlear nucleus. J Neurophysiol 50:1156–1181
Marsh JT, Worden FG, Smith JC (1970) Auditory frequency-following response: neural or artifact? Science 169:1222–1223
Nicholson C, Freeman JA (1975) Theory of current source-density analysis and determination of conductivity tensor for anuran cerebellum. J Neurophysiol 38:356–368
Schwartz IR (1977) Dendritic arrangements in the cat medial superior olive. Neuroscience 2:81–101
Schwarz DW (1992) Can central neurons reproduce sound waveforms? An analysis of the neurophonic potential in the laminar nucleus of the chicken. J Otolaryngol 21:30–38
Scott LL, Hage TA, Golding NL (2007) Weak action potential backpropagation is associated with high-frequency axonal firing capability in principal neurons of the gerbil medial superior olive. J Physiol 583:647–661
Smith PH (1995) Structural and functional differences distinguish principal from nonprincipal cells in the guinea pig MSO slice. J Neurophysiol 73:1653–1667
Snyder RL, Schreiner CE (1984) The auditory neurophonic: basic properties. Hear Res 15:261–280
Stotler WA (1953) An experimental study of the cells and connections of the superior olivary complex of the cat. J Comp Neurol 98:401–431
Sullivan WE, Konishi M (1986) Neural map of interaural phase difference in the owl’s brainstem. Proc Natl Acad Sci U S A 83:8400–8404
Yin TCT, Chan JK (1990) Interaural time sensitivity in medial superior olive of cat. J Neurophysiol 64:465–488
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2010 Springer Science+Business Media, LLC
About this paper
Cite this paper
Laughlin, M.M., van der Heijden, M., Joris, P.X. (2010). Phase Shifts in Monaural Field Potentials of the Medial Superior Olive. In: Lopez-Poveda, E., Palmer, A., Meddis, R. (eds) The Neurophysiological Bases of Auditory Perception. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-5686-6_35
Download citation
DOI: https://doi.org/10.1007/978-1-4419-5686-6_35
Published:
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4419-5685-9
Online ISBN: 978-1-4419-5686-6
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)