|
|
||||||||
Journal of Neurophysiology, Vol 73, Issue 2 743-765, Copyright © 1995 by APS
ARTICLES |
E. D. Young, I. Nelken and R. A. Conley
Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205, USA.
1. Single units and evoked potentials were recorded in dorsal cochlear nucleus (DCN) in response to electrical stimulation of the somatosensory dorsal column and spinal trigeminal nuclei (together called MSN for medullary somatosensory nuclei) and for tactile somatosensory stimuli. Recordings were from paralyzed decerebrate cats. 2. DCN principal cells (type IV units) were strongly inhibited by electrical stimulation (single 50-microA bipolar pulse) in MSN or by somatosensory stimulation. Units recorded in the fusiform cell and deep layers of DCN were inhibited, suggesting that the inhibition affects both types of principal cells (i.e., both fusiform and giant cells). 3. Interneurons (type II units) that inhibit principal cells were only weakly inhibited by electrical stimulation and were never excited, demonstrating that the inhibitory effect on principal cells does not pass through the type II circuit. In the vicinity of the DCN/PVCN (posteroventral cochlear nucleus) boundary, units were encountered that were excited by electrical stimulation in MSN; some of these neurons responded to sound, and some did not. Their response properties are consistent with the hypothesis that they are deep-layer inhibitory interneurons conveying somatosensory information to the DCN. 4. Analysis of the evoked potentials produced by electrical stimulation in MSN suggests that the somatosensory inputs activate the granule cell system of the DCN molecular layer. A model based on previous work by Klee and Rall was used to show that the distribution of evoked potentials in DCN can be explained as resulting from radial currents produced in the DCN molecular and fusiform-cell layers by synchronous activation of granule cells inputs to fusiform and cartwheel cells. Current-source density analysis of the evoked potentials is consistent with this model. Thus molecular layer interneurons (cartwheel and stellate cells) are a second possible source of inhibition to principal cells. 5. With lower stimulus levels (20 microA) and pulse-pair stimuli (50- to 100-ms interstimulus interval), three components of the inhibitory response can be recognized in both fusiform cell layer and deep layer type IV units: a short-latency inhibition that begins before the start of the evoked potential; a longer-latency inhibition whose timing corresponds to the evoked potential; and an excitatory component that occurs on the rising phase of the evoked potential. The excitatory component is usually overwhelmed by the inhibitory components and could be derived from granule cell inputs; the long-latency inhibitory component could be derived from cartwheel cells or the hypothesized deep-layer inhibitory interneurons.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
C. V. Portfors and P. D. Roberts Temporal and Frequency Characteristics of Cartwheel Cells in the Dorsal Cochlear Nucleus of the Awake Mouse J Neurophysiol, August 1, 2007; 98(2): 744 - 756. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. O. Kanold and P. B. Manis Encoding the Timing of Inhibitory Inputs J Neurophysiol, May 1, 2005; 93(5): 2887 - 2897. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. Behrend, B. Dickson, E. Clarke, C. Jin, and S. Carlile Neural Responses to Free Field and Virtual Acoustic Stimulation in the Inferior Colliculus of the Guinea Pig J Neurophysiol, November 1, 2004; 92(5): 3014 - 3029. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. S. Malmierca, M. A. Merchan, C. K. Henkel, and D. L. Oliver Direct Projections from Cochlear Nuclear Complex to Auditory Thalamus in the Rat J. Neurosci., December 15, 2002; 22(24): 10891 - 10897. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M Baguley Mechanisms of tinnitus Br. Med. Bull., October 1, 2002; 63(1): 195 - 212. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. E. Hancock and H. F. Voigt Intracellularly Labeled Fusiform Cells in Dorsal Cochlear Nucleus of the Gerbil. I. Physiological Response Properties J Neurophysiol, May 1, 2002; 87(5): 2505 - 2519. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. O. Kanold and E. D. Young Proprioceptive Information from the Pinna Provides Somatosensory Input to Cat Dorsal Cochlear Nucleus J. Neurosci., October 1, 2001; 21(19): 7848 - 7858. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. O. Kanold and P. B. Manis A Physiologically Based Model of Discharge Pattern Regulation by Transient K+ Currents in Cochlear Nucleus Pyramidal Cells J Neurophysiol, February 1, 2001; 85(2): 523 - 538. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Davis and E. D. Young Pharmacological Evidence of Inhibitory and Disinhibitory Neuronal Circuits in Dorsal Cochlear Nucleus J Neurophysiol, February 1, 2000; 83(2): 926 - 940. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Ding, T. E. Benson, and H. F. Voigt Acoustic and Current-Pulse Responses of Identified Neurons in the Dorsal Cochlear Nucleus of Unanesthetized, Decerebrate Gerbils J Neurophysiol, December 1, 1999; 82(6): 3434 - 3457. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. A. Spirou, K. A. Davis, I. Nelken, and E. D. Young Spectral Integration by Type II Interneurons in Dorsal Cochlear Nucleus J Neurophysiol, August 1, 1999; 82(2): 648 - 663. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. S. Rhode Vertical Cell Responses to Sound in Cat Dorsal Cochlear Nucleus J Neurophysiol, August 1, 1999; 82(2): 1019 - 1032. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. O. Kanold and P. B. Manis Transient Potassium Currents Regulate the Discharge Patterns of Dorsal Cochlear Nucleus Pyramidal Cells J. Neurosci., March 15, 1999; 19(6): 2195 - 2208. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. X. Joris and P. H. Smith Temporal and Binaural Properties in Dorsal Cochlear Nucleus and Its Output Tract J. Neurosci., December 1, 1998; 18(23): 10157 - 10170. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. W. H. Schnupp, A. J. King, and S. Carlile Altered Spectral Localization Cues Disrupt the Development of the Auditory Space Map in the Superior Colliculus of the Ferret J Neurophysiol, February 1, 1998; 79(2): 1053 - 1069. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Davis and E. D. Young Granule Cell Activation of Complex-Spiking Neurons in Dorsal Cochlear Nucleus J. Neurosci., September 1, 1997; 17(17): 6798 - 6806. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Davis and H. F. Voigt Evidence of Stimulus-Dependent Correlated Activity in the Dorsal Cochlear Nucleus of Decerebrate Gerbils J Neurophysiol, July 1, 1997; 78(1): 229 - 247. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. L. Golding and D. Oertel Physiological Identification of the Targets of Cartwheel Cells in the Dorsal Cochlear Nucleus J Neurophysiol, July 1, 1997; 78(1): 248 - 260. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Ding and H. F. Voigt Intracellular Response Properties of Units in the Dorsal Cochlear Nucleus of Unanesthetized Decerebrate Gerbil J Neurophysiol, May 1, 1997; 77(5): 2549 - 2572. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |