Literature DB >> 2918341

Responses to parallel fiber stimulation in the guinea pig dorsal cochlear nucleus in vitro.

P B Manis1.   

Abstract

1. Parallel fibers of the guinea pig dorsal cochlear nucleus (DCN) were electrically stimulated at the pial surface of the nucleus in a brain-slice preparation. Extracellular field potentials produced by the parallel fibers and postsynaptic cells, and the response of single units were identified and characterized. Responses were compared with those reported for stimulation of parallel fibers in the cerebellum and to those seen with electrical stimulation of the auditory nerve. 2. Stimulation of the DCN parallel fibers generates a consistent set of extracellular field potentials. In layer 1 of the DCN, a short-latency triphasic wave (P1(1)-N1(1)-P2(1)) is followed by a slower negative wave (N2(1)). The onset phase of the N2(1) often exhibits a small positive notch (P2a1). In layer 2, an initial triphasic wave (P1(2)-N1(2)-P2(2)) is followed by a short-latency negative wave (N2(2)) and a slower positive wave (P3(2)). The N1(2) is approximately coincident with the N1(1), whereas the P3(2) is coincident with N2(1). The falling phase of the P3(2) is sometimes interrupted by a brief negative deflection (N3(2)). These field potentials are similar, but not identical to those reported for parallel fiber stimulation in the cerebellum in vivo (15). These responses differ substantially from those produced in the DCN by electrical stimulation of the auditory nerve (50). 3. Low-calcium solutions and pharmacologic manipulations were used to separate pre- and postsynaptic response components in the field potential records. When the slice is bathed in a low-calcium solution the P2a1, N2(1), N2(2), P3(2), and the brief late deflections are abolished. However, the P1(1)-N1(1)-P2(1) and P1(2)-N1(2)-P2(2) remain unaffected. A similar separation of pre- and postsynaptic components can be achieved with 100 microM adenosine or 0.5 mM kynurenic acid. It is concluded that the P1(1)-M1(1)-P2(1) wave is the compound action potential of the unmyelinated parallel fibers, whereas the longer-latency field potential components are generated postsynaptically. 4. The conduction velocity of the parallel fiber volley was measured to be 0.30 m/s at the pial surface, in a line approximately parallel to the strial axis of the nucleus. Mapping experiments reveal that the spread of the P1(1)-N1(1)-P2(1) is greatest along the strial axis, and more limited in the orthogonal direction. 5. Single units were recorded in layer 2. At a distance of 500-700 microns from the stimulating electrode, the latencies of single-unit discharges fall between 2.5 and 4 ms, at the time of the N2(2).(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1989        PMID: 2918341     DOI: 10.1152/jn.1989.61.1.149

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  15 in total

1.  Projections of the second cervical dorsal root ganglion to the cochlear nucleus in rats.

Authors:  Xiping Zhan; Tan Pongstaporn; David K Ryugo
Journal:  J Comp Neurol       Date:  2006-05-20       Impact factor: 3.215

2.  Projections of low spontaneous rate, high threshold auditory nerve fibers to the small cell cap of the cochlear nucleus in cats.

Authors:  D K Ryugo
Journal:  Neuroscience       Date:  2007-11-17       Impact factor: 3.590

3.  Stimulus-dependent changes in optical responses of the dorsal cochlear nucleus using voltage-sensitive dye.

Authors:  F G Licari; M Shkoukani; J A Kaltenbach
Journal:  J Neurophysiol       Date:  2011-05-04       Impact factor: 2.714

4.  Granule cell activation of complex-spiking neurons in dorsal cochlear nucleus.

Authors:  K A Davis; E D Young
Journal:  J Neurosci       Date:  1997-09-01       Impact factor: 6.167

5.  Action potential propagation and propagation block by GABA in rat posterior pituitary nerve terminals.

Authors:  M B Jackson; S J Zhang
Journal:  J Physiol       Date:  1995-03-15       Impact factor: 5.182

6.  Target- and input-dependent organization of AMPA and NMDA receptors in synaptic connections of the cochlear nucleus.

Authors:  María E Rubio; Yugo Fukazawa; Naomi Kamasawa; Cheryl Clarkson; Elek Molnár; Ryuichi Shigemoto
Journal:  J Comp Neurol       Date:  2014-07-29       Impact factor: 3.215

7.  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

8.  Distribution and targets of the cartwheel cell axon in the dorsal cochlear nucleus of the guinea pig.

Authors:  A S Berrebi; E Mugnaini
Journal:  Anat Embryol (Berl)       Date:  1991

9.  Suppression of noise-induced hyperactivity in the dorsal cochlear nucleus following application of the cholinergic agonist, carbachol.

Authors:  N F Manzoor; G Chen; J A Kaltenbach
Journal:  Brain Res       Date:  2013-05-27       Impact factor: 3.252

10.  Cochlear damage changes the distribution of vesicular glutamate transporters associated with auditory and nonauditory inputs to the cochlear nucleus.

Authors:  Chunhua Zeng; Nishant Nannapaneni; Jianxun Zhou; Larry F Hughes; Susan Shore
Journal:  J Neurosci       Date:  2009-04-01       Impact factor: 6.167

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