Literature DB >> 20394063

Connections of the auditory brainstem in a songbird, Taeniopygia guttata. III. Projections of the superior olive and lateral lemniscal nuclei.

J Martin Wild1, Nils O E Krützfeldt, M Fabiana Kubke.   

Abstract

Sequential to companion articles that report the projections of the cochlear nucleus angularis (NA) and the third-order nucleus laminaris (NL) to the central nucleus of the inferior colliculus (MLd) and to the superior olive (OS) and lateral lemniscal nuclei (LLV, LLI, and LLD) (Krützfeldt et al., J Comp Neurol, this issue), we here describe the projections of the latter group of nuclei using standard tract-tracing methods. OS projects on LLV and both have further ascending projections on LLI, LLD, and MLd. LLV also provides auditory input to the song system, via nucleus uvaeformis, and to the thalamo-telencephalic auditory system, via nucleus ovoidalis (Ov), thus bypassing MLd. The two divisions of LLD (LLDa and LLDp) project across the midline via the commissure of Probst each to innervate the homologous contralateral nucleus and MLd. Both, particularly LLDp, also project on Ov. Injections in LLD and LLV resulted in anterograde labeling of caudal nucleus basorostralis (Bas) in the frontal telencephalon, but retrograde tracing so far suggests that only LLI is a real source of this projection (Wild and Farabaugh [1996] J Comp Neurol 365:306-328). OS and LLV also have descending projections on the ipsilateral NA, NM, and NL, and LLV also projects on OS. The ascending inputs to MLd and more rostral nuclei may contribute importantly to mechanisms of auditory pattern (song) recognition. Consistent with previous studies, some of the descending projections may be inhibitory. (c) 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20394063      PMCID: PMC3865895          DOI: 10.1002/cne.22325

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  62 in total

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4.  GABAergic neurons in brainstem auditory nuclei of the chick: distribution, morphology, and connectivity.

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5.  The role of GABAergic inhibition in processing of interaural time difference in the owl's auditory system.

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6.  Connections of the auditory forebrain in the pigeon (Columba livia).

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7.  Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies.

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8.  Auditory projections to the anterior telencephalon in the budgerigar (Melopsittacus undulatus).

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9.  Commissural connections mediate inhibition for the computation of interaural level difference in the barn owl.

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10.  Development of GABA immunoreactivity in brainstem auditory nuclei of the chick: ontogeny of gradients in terminal staining.

Authors:  R A Code; G D Burd; E W Rubel
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  18 in total

Review 1.  Advantages of comparative studies in songbirds to understand the neural basis of sensorimotor integration.

Authors:  Karagh Murphy; Logan S James; Jon T Sakata; Jonathan F Prather
Journal:  J Neurophysiol       Date:  2017-03-22       Impact factor: 2.714

2.  Connections of the auditory brainstem in a songbird, Taeniopygia guttata. I. Projections of nucleus angularis and nucleus laminaris to the auditory torus.

Authors:  Nils O E Krützfeldt; Priscilla Logerot; M Fabiana Kubke; J Martin Wild
Journal:  J Comp Neurol       Date:  2010-06-01       Impact factor: 3.215

3.  Connections of the auditory brainstem in a songbird, Taeniopygia guttata. II. Projections of nucleus angularis and nucleus laminaris to the superior olive and lateral lemniscal nuclei.

Authors:  Nils O E Krützfeldt; Priscilla Logerot; M Fabiana Kubke; J Martin Wild
Journal:  J Comp Neurol       Date:  2010-06-01       Impact factor: 3.215

4.  Tonotopic organization of the superior olivary nucleus in the chicken auditory brainstem.

Authors:  Kathryn M Tabor; William L Coleman; Edwin W Rubel; R Michael Burger
Journal:  J Comp Neurol       Date:  2012-05-01       Impact factor: 3.215

5.  Organization of the auditory brainstem in a lizard, Gekko gecko. I. Auditory nerve, cochlear nuclei, and superior olivary nuclei.

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6.  Topography and morphology of the inhibitory projection from superior olivary nucleus to nucleus laminaris in chickens (Gallus gallus).

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Review 8.  Early experience shapes vocal neural coding and perception in songbirds.

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Review 9.  Coevolution in communication senders and receivers: vocal behavior and auditory processing in multiple songbird species.

Authors:  Sarah M N Woolley; Jordan M Moore
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10.  Second tectofugal pathway in a songbird (Taeniopygia guttata) revisited: Tectal and lateral pontine projections to the posterior thalamus, thence to the intermediate nidopallium.

Authors:  J Martin Wild; Andrea H Gaede
Journal:  J Comp Neurol       Date:  2015-09-03       Impact factor: 3.215

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