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Spatiotemporal Analysis of Cochlear Nucleus Innervation by Spiral Ganglion Neurons that Serve Distinct Regions of the Cochlea
2020, NeuroscienceCitation Excerpt :Another plausible mechanism is axon pruning. Using histological staining, electrophysiological recording, and anatomic tracing, it has been shown that axonal pruning of ANF branches occurs in the avian AVCN (nucleus magnocellularis) (Jackson and Parks, 1982; Jhaveri and Morest, 1982). Elimination of axon branching during postnatal refinement of ANFs could also take place in our case, with both pre-hearing spontaneous activity and post-hearing sensory experience likely to play a role in this process (Babola et al., 2018; Clause et al., 2014; Connelly et al., 2017; Leake et al., 2002; Lee et al., 2003; Muller et al., 2019; Singer et al., 2014; Wang and Bergles, 2015).
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2020, The Senses: A Comprehensive Reference: Volume 1-7, Second EditionTonotopic Differentiation of Coupling between Ca<sup>2+</sup> and Kv1.1 Expression in Brainstem Auditory Circuit
2019, iScienceCitation Excerpt :The morphology of NM neurons developed during the course of culture; the neurons showed multipolar shape and several dendrites at 1DIV but became spherical shape and decreased the number of dendrites by 14DIV (Figure 1D). Importantly, the loss of dendrites was more prominent in higher-CF neurons, making the neurons almost adendritic at 14DIV (Figure 1F), which resembled the morphological development in vivo (Jhaveri and Morest, 1982). Cross-sectional area of the soma increased with development and became similar between high- and low-CF neurons (Figure 1E).
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2015, Hearing ResearchFiring properties of auditory primary afferents from the basilar papilla in the chick
2015, International Journal of Developmental NeuroscienceCitation Excerpt :However, this is different in the chick's auditory system, where such a subdivision of afferent neurons or hair cells does not exist, and of course, a bouton and calyx terminal division is not present; therefore the functional roles of each afferent fiber type must be related to a different cause (Shimazu and Precht, 1965; Babalian et al., 1997; Beraneck and Straka, 2011). Our results are consistent with the current knowledge about sound responses (Jones and Jones, 2006) and development of spontaneous activity (Manley et al., 1991; Jones and Jones, 2000), along with the morphological and functional changes already described for the chick’s auditory system, at both peripheral and central auditory relays (Tilney et al., 1986; Si et al., 2003; Jhaveri and Morest, 1982). All these changes points out the period between E18-E19 as the early stage where most of the characteristics considered as permissive for auditory processing are present.
From development to disease: Diverse functions of NMDA-type glutamate receptors in the lower auditory pathway
2015, NeuroscienceCitation Excerpt :Neurons in VCN and NM reliably process auditory information through specialized endbulb of Held synapses (Adams, 1986; Carr and Boudreau, 1991; Koppl, 1994). Numerous endbulb synapses are eliminated during development such that only two or three large terminals contact one cell body (Jhaveri and Morest, 1982; Ryugo et al., 2006; Lu and Trussell, 2007). This synaptic pruning takes place during a time period when GluN2B-containing NMDA-R responses dominate (Bellingham et al., 1998; Lu and Trussell, 2007).
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Present address: Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, MA 02139, U.S.A.