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Relevant bibliographies by topics / Spherical Bushy Cells

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Journal articles

Academic literature on the topic 'Spherical Bushy Cells'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Spherical Bushy Cells"

1

Keine, Christian, and Rudolf Rübsamen. "Inhibition Shapes Acoustic Responsiveness in Spherical Bushy Cells." Journal of Neuroscience 35, no. 22 (2015): 8579–92. http://dx.doi.org/10.1523/jneurosci.0133-15.2015.

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2

Keine, Christian, and Rudolf Rübsamen. "Inhibition shapes acoustic responsiveness in spherical bushy cells." Journal of Neuroscience 35, no. 22 (2015): 8597–92. https://doi.org/10.1523/JNEUROSCI.0133-15.2015.

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Signal processing in the auditory brainstem is based on an interaction of neuronal excitation and inhibition. To date, we have incomplete knowledge of how the dynamic interplay of both contributes to the processing power and temporal characteristics of signal coding. The spherical bushy cells (SBCs) of the anteroventral cochlear nucleus (AVCN) receive their primary excitatory input through auditory nerve fibers via large, axosomatic synaptic terminals called the endbulbs of Held and by additional, acoustically driven inhibitory inputs. SBCs provide the input to downstream nuclei of the brainst

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3

Cao, Xiao-Jie, and Donata Oertel. "Auditory Nerve Fibers Excite Targets Through Synapses That Vary in Convergence, Strength, and Short-Term Plasticity." Journal of Neurophysiology 104, no. 5 (2010): 2308–20. http://dx.doi.org/10.1152/jn.00451.2010.

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Auditory nerve fibers are the major source of excitation to the three groups of principal cells of the ventral cochlear nucleus (VCN), bushy, T stellate, and octopus cells. Shock-evoked excitatory postsynaptic currents (eEPSCs) in slices from mice showed systematic differences between groups of principal cells, indicating that target cells contribute to determining pre- and postsynaptic properties of synapses from spiral ganglion cells. Bushy cells likely to be small spherical bushy cells receive no more than three, most often two, excitatory inputs; those likely to be globular bushy cells rec

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4

Gillet, Charlène, Stefanie Kurth, and Thomas Kuenzel. "Muscarinic modulation of M and h currents in gerbil spherical bushy cells." PLOS ONE 15, no. 1 (2020): e0226954. http://dx.doi.org/10.1371/journal.pone.0226954.

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5

Koert, Elisabeth, and Thomas Kuenzel. "Small dendritic synapses enhance temporal coding in a model of cochlear nucleus bushy cells." Journal of Neurophysiology 125, no. 3 (2021): 915–37. http://dx.doi.org/10.1152/jn.00331.2020.

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We modeled dendritic inputs from the auditory nerve that spherical bushy cells of the cochlear nucleus receive. Dendritic inputs caused both tonic depolarization and modulation of the membrane potential at the input frequency. This improved the rate, entrainment, and temporal precision of output action potentials. Our simulations suggest a role for small dendritic inputs in auditory processing: they modulate the efficacy of the main input supporting temporal precision and fidelity in these central auditory neurons.

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6

Nerlich, Jana, Thomas Kuenzel, Christian Keine, Andrej Korenic, Rudolf Rübsamen, and Ivan Milenkovic. "Dynamic fidelity control to the central auditory system: synergistic glycine/GABAergic inhibition in the cochlear nucleus." Journal of Neuroscience 34, no. 35 (2014): 11604–20. https://doi.org/10.1523/JNEUROSCI.0719-14.2014.

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GABA and glycine are the major inhibitory transmitters that attune neuronal activity in the CNS of mammals. The respective transmitters are mostly spatially separated, that is, synaptic inhibition in the forebrain areas is mediated by GABA, whereas glycine is predominantly used in the brainstem. Accordingly, inhibition in auditory brainstem circuits is largely mediated by glycine, but there are few auditory synapses using both transmitters in maturity. Little is known about physiological advantages of such a two-transmitter inhibitory mechanism. We explored the benefit of engaging both glycine

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7

Milenkovic, Ivan, Ilka Rinke, Mirko Witte, Beatrice Dietz, and Rudolf Rübsamen. "P2 Receptor–Mediated Signaling in Spherical Bushy Cells of the Mammalian Cochlear Nucleus." Journal of Neurophysiology 102, no. 3 (2009): 1821–33. http://dx.doi.org/10.1152/jn.00186.2009.

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Purinoreceptors of the P2 family contribute strongly to signaling in the cochlea, but little is known about the effects of purinergic neurotransmission in the central auditory system. Here we examine P2 receptor–mediated signaling in the large spherical bushy cells (SBCs) of Mongolian gerbils around the onset of acoustically evoked signal processing (P9–P14). Brief adenosine 5′-O-(3-thiotriphosphate) (ATPγS) application evoked inward current, membrane depolarization, and somatic Ca2+ signals. Moreover, ATPγS changed the SBCs firing pattern from phasic to tonic, when the application was synchro

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8

Schwarz, Dietrich W. F., and Ernest Puil. "Firing properties of spherical bushy cells in the anteroventral cochlear nucleus of the gerbil." Hearing Research 114, no. 1-2 (1997): 127–38. http://dx.doi.org/10.1016/s0378-5955(97)00162-7.

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9

Sento, Seishiro, and David K. Ryugo. "Endbulbs of held and spherical bushy cells in cats: Morphological correlates with physiological properties." Journal of Comparative Neurology 280, no. 4 (1989): 553–62. http://dx.doi.org/10.1002/cne.902800406.

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10

Keine, Christian, Rudolf Rübsamen, and Bernhard Englitz. "Signal integration at spherical bushy cells enhances representation of temporal structure but limits its range." eLife 6 (September 25, 2017): 29639. https://doi.org/10.5281/zenodo.1001813.

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Neuronal inhibition is crucial for temporally precise and reproducible signaling in the auditory brainstem. We showed previously (Keine et al., 2016) that for various synthetic stimuli, spherical bushy cell (SBC) activity in the Mongolian gerbil is rendered sparser and more reliable by subtractive inhibition. Employing environmental stimuli, we demonstrate here that the inhibitory gain control becomes even more effective, keeping stimulated response rates equal to spontaneous ones. However, what are the costs of this modulation? We performed dynamic stimulus reconstructions based on neural pop

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