1986
DOI: 10.1002/cne.902470406
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Projections from the anteroventral cochlear nucleus to the lateral and medial superior olivary nuclei

Abstract: The projections from the cochlear nucleus to the lateral and medial superior olivary nuclei were studied in the cat by use of retrograde transport of horseradish peroxidase to demonstrate the connections. The medial superior olivary nucleus receives input only from the anterior and posterodorsal subdivisions of the anterior division of the anteroventral cochlear nucleus (AA and APD, respectively; Brawer, Morest, and Kane: J. Comp. Neurol. 155: 251-300, 1974). These two subdivisions are populated almost exclusi… Show more

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Cited by 273 publications
(173 citation statements)
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“…The first stage is a phenomenological model of ANFs that produces realistic temporal discharge patterns to both acoustic pure tones and electric pulse trains (Nourski et al 2006). MSO neurons receive bilateral excitatory inputs from ANFs via spherical bushy cells (SBCs) in the VCN, as well as bilateral inhibitory inputs originating from globular bushy cells in the VCN (Cant and Casseday 1986;Smith et al 1993). In our implementation, the SBC stage was omitted because SBC shows little coincidence detection themselves (Wang and Delgutte 2012).…”
Section: Methodsmentioning
confidence: 99%
“…The first stage is a phenomenological model of ANFs that produces realistic temporal discharge patterns to both acoustic pure tones and electric pulse trains (Nourski et al 2006). MSO neurons receive bilateral excitatory inputs from ANFs via spherical bushy cells (SBCs) in the VCN, as well as bilateral inhibitory inputs originating from globular bushy cells in the VCN (Cant and Casseday 1986;Smith et al 1993). In our implementation, the SBC stage was omitted because SBC shows little coincidence detection themselves (Wang and Delgutte 2012).…”
Section: Methodsmentioning
confidence: 99%
“…It is comprised of diverse and highly specialised neuronal populations (Ram on y Cajal c.1900;Lorente de N o, 1933Lorente de N o, , 1981 differing in morphology (Harrison and Warr, 1962;Osen, 1969a;and 1969b;Brawer et al, 1974;Heiman-Patterson and Strominger, 1985;Adams, 1986), response properties (Pfeiffer and Kiang, 1965;Pfeiffer, 1966;Evans and Nelson, 1973;Shofner and Young, 1985;Blackburn and Sachs, 1989;Winter and Palmer, 1990;Marsh et al, 2006), and connectivity with the auditory nerve (Liberman, 1991(Liberman, , 1993. Each neuronal population in the CN exhibits distinct projections (summarised in Cant and Benson, 2003), some ipsilateral (Cant and Casseday, 1986), others contralateral (Warr, 1966(Warr, , 1969Winer and Schreiner, 2005), reflecting the distinct functions of the CN anteroventral (involved in sound localisation) and posteroventral regions (involved in sound discrimination) (Eggermont, 2001).…”
Section: Cochlear Nucleusmentioning
confidence: 99%
“…Type V units are binaurally excited (EE) and exhibit the "peak" binaural delay that is typically observed in the medial superior olive (MSO) Ramachandran and May 2002). Because spherical bushy cells (SBCs) in the anterior subdivision of the VCN project bilaterally to the MSO (Cant and Casseday 1986;Smith et al 1993), the dominant ascending inputs of type V units originate in the VCN.…”
Section: Type X and Tail Unitsmentioning
confidence: 99%
“…Median SR is based only on spontaneously active units with BFs within two octaves of the EDGE suggest that their binaural responses are dictated by inputs from the lateral superior olive (LSO) (Ramachandran and May 2002). The LSO receives excitatory inputs from SBCs in the ipsilateral VCN (Cant and Casseday 1986;Cant and Benson 2003). Inhibitory inputs originate in the ipsilateral medial nucleus of the trapezoid body (MNTB) which are driven by globular bushy cells (GBCs) in the contralateral VCN (Kuwabara et al 1991;Smith et al 1991).…”
Section: Type X and Tail Unitsmentioning
confidence: 99%