Literature DB >> 11549753

Correlation of AMPA receptor subunit composition with synaptic input in the mammalian cochlear nuclei.

S M Gardner1, L O Trussell, D Oertel.   

Abstract

The composition of AMPA receptors in patches excised from somata and dendrites of six cell types in the mammalian cochlear nuclei was probed and compared electrophysiologically and pharmacologically with the rapid application of glutamate. Cells excited predominantly by auditory nerve fibers had AMPA receptors with exceptionally rapid gating (submillisecond deactivation and desensitization time constants). The nonlinear current-voltage relationship in the presence of spermine showed that few of these receptors had GluR2 subunits, and the insensitivity of desensitization to cyclothiazide indicated that they contained mostly flop splice variants. At synapses made by parallel fibers, AMPA receptors were slowly gating (time constants of deactivation and desensitization >1 msec) and contained higher levels of GluR2 and flip isoforms. However, receptors at auditory nerve synapses on cells that also receive parallel fiber input, the fusiform cells, had intermediate properties with respect to kinetics and contained GluR2 and flip isoforms. Given the diverse biophysical properties, patterns of innervation, patterns of electrical activity, and targets of each cell type in vivo, these data indicate that the kinetics and permeation properties of AMPA receptors are linked to factors associated with synaptic connectivity.

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Year:  2001        PMID: 11549753      PMCID: PMC6763000     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  71 in total

1.  Expression of AMPA receptor subunit flip/flop splice variants in the rat auditory brainstem and inferior colliculus.

Authors:  S Schmid; A Guthmann; J P Ruppersberg; H Herbert
Journal:  J Comp Neurol       Date:  2001-02-05       Impact factor: 3.215

2.  RNA editing in brain controls a determinant of ion flow in glutamate-gated channels.

Authors:  B Sommer; M Köhler; R Sprengel; P H Seeburg
Journal:  Cell       Date:  1991-10-04       Impact factor: 41.582

3.  Intracellular polyamines mediate inward rectification of Ca(2+)-permeable alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors.

Authors:  S D Donevan; M A Rogawski
Journal:  Proc Natl Acad Sci U S A       Date:  1995-09-26       Impact factor: 11.205

4.  Control of kinetic properties of AMPA receptor channels by nuclear RNA editing.

Authors:  H Lomeli; J Mosbacher; T Melcher; T Höger; J R Geiger; T Kuner; H Monyer; M Higuchi; A Bach; P H Seeburg
Journal:  Science       Date:  1994-12-09       Impact factor: 47.728

5.  Electron microscopic features of physiologically characterized, HRP-labeled fusiform cells in the cat dorsal cochlear nucleus.

Authors:  P H Smith; W S Rhode
Journal:  J Comp Neurol       Date:  1985-07-01       Impact factor: 3.215

6.  Contrasting molecular composition and channel properties of AMPA receptors on chick auditory and brainstem motor neurons.

Authors:  A Ravindranathan; S D Donevan; S G Sugden; A Greig; M S Rao; T N Parks
Journal:  J Physiol       Date:  2000-03-15       Impact factor: 5.182

7.  Block of native Ca(2+)-permeable AMPA receptors in rat brain by intracellular polyamines generates double rectification.

Authors:  D S Koh; N Burnashev; P Jonas
Journal:  J Physiol       Date:  1995-07-15       Impact factor: 5.182

8.  Inward rectification of both AMPA and kainate subtype glutamate receptors generated by polyamine-mediated ion channel block.

Authors:  D Bowie; M L Mayer
Journal:  Neuron       Date:  1995-08       Impact factor: 17.173

9.  Two separate inhibitory mechanisms shape the responses of dorsal cochlear nucleus type IV units to narrowband and wideband stimuli.

Authors:  I Nelken; E D Young
Journal:  J Neurophysiol       Date:  1994-06       Impact factor: 2.714

10.  Quantal analysis of EPSCs recorded from small numbers of synapses in hippocampal cultures.

Authors:  J M Bekkers; C F Stevens
Journal:  J Neurophysiol       Date:  1995-03       Impact factor: 2.714

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  49 in total

1.  Bidirectional synaptic plasticity in the cerebellum-like mammalian dorsal cochlear nucleus.

Authors:  Kiyohiro Fujino; Donata Oertel
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-16       Impact factor: 11.205

2.  Distinct AMPA-type glutamatergic synapses in developing rat CA1 hippocampus.

Authors:  Elizabeth A Stubblefield; Tim A Benke
Journal:  J Neurophysiol       Date:  2010-08-04       Impact factor: 2.714

Review 3.  Ras and Rap signaling in synaptic plasticity and mental disorders.

Authors:  Ruth L Stornetta; J Julius Zhu
Journal:  Neuroscientist       Date:  2010-04-29       Impact factor: 7.519

4.  Ultrastructure, synaptic organization, and molecular components of bushy cell networks in the anteroventral cochlear nucleus of the rhesus monkey.

Authors:  R Gómez-Nieto; M E Rubio
Journal:  Neuroscience       Date:  2011-02-01       Impact factor: 3.590

5.  Action potential timing precision in dorsal cochlear nucleus pyramidal cells.

Authors:  Sarah E Street; Paul B Manis
Journal:  J Neurophysiol       Date:  2007-04-18       Impact factor: 2.714

6.  Auditory nerve inputs to cochlear nucleus neurons studied with cross-correlation.

Authors:  E D Young; M B Sachs
Journal:  Neuroscience       Date:  2008-02-05       Impact factor: 3.590

7.  Voltage-activated calcium currents in octopus cells of the mouse cochlear nucleus.

Authors:  Ramazan Bal; Donata Oertel
Journal:  J Assoc Res Otolaryngol       Date:  2007-08-21

8.  Amplitude Normalization of Dendritic EPSPs at the Soma of Binaural Coincidence Detector Neurons of the Medial Superior Olive.

Authors:  Bradley D Winters; Shan-Xue Jin; Kenneth R Ledford; Nace L Golding
Journal:  J Neurosci       Date:  2017-02-17       Impact factor: 6.167

Review 9.  Beyond timing in the auditory brainstem: intensity coding in the avian cochlear nucleus angularis.

Authors:  Katrina M MacLeod; Catherine E Carr
Journal:  Prog Brain Res       Date:  2007       Impact factor: 2.453

10.  Chemical synaptic transmission onto superficial stellate cells of the mouse dorsal cochlear nucleus.

Authors:  Pierre F Apostolides; Laurence O Trussell
Journal:  J Neurophysiol       Date:  2014-02-12       Impact factor: 2.714

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