|
|
||||||||
Journal of Neurophysiology, Vol 63, Issue 4 767-780, Copyright © 1990 by APS
ARTICLES |
C. Fernandez, J. M. Goldberg and R. A. Baird
Department of Surgery (Otolaryngology-Head and Neck Surgery), University of Chicago, Illinois 60637.
1. Nerve fibers supplying the utricular macula of the chinchilla were labeled by extracellular injection of horseradish peroxidase into the vestibular nerve. The peripheral terminations of individual fibers were reconstructed and related to the regions of the end organ they innervated and to the sizes of their parent axons. 2. The macula is divided into medial and lateral parts by the striola, a narrow zone that runs for almost the entire length of the sensory epithelium. The striola can be distinguished from the extrastriolar regions to either side of it by the wider spacing of its hair cells. Calyx endings in the striola have especially thick walls, and, unlike similar endings in the extrastriola, many of them innervate more than one hair cell. The striola occupies 10% of the sensory epithelium; the lateral extrastriola, 50%; and the medial extrastriola, 40%. 3. The utricular nerve penetrates the bony labyrinth anterior to the end organ. Axons reaching the anterior part of the sensory epithelium run directly through the connective tissue stroma. Those supplying more posterior regions first enter a fiber layer located at the bottom of the stroma. Approximately one-third of the axons bifurcate below the epithelium, usually within 5-20 microns of the basement membrane. Bifurcations are more common in fibers destined for the extrastriola than for the striola. 4. Both calyx and bouton endings were labeled. Calyces can be simple or complex. Simple calyces innervate individual hair cells, whereas complex calyces supply 2-4 adjacent hair cells. Complex endings are more heavily concentrated in the striola than in the extrastriola. Simple calyces and boutons are found in all parts of the epithelium. Calyces emerge from the parent axon or one of its thick branches. Boutons, whether en passant or terminal, are located on thin collaterals. 5. Fibers can be classified into calyx, bouton, or dimorphic categories. The first type only has calyx endings; the second, only bouton endings; and the third, both kinds of endings. Calyx units make up 6% of the labeled fibers, bouton units less than 2%, and dimorphic units greater than 92%. The three fiber types differ in the macular zones they supply and in the diameters of their parent axons. Calyx units were restricted to the striola. The few bouton units were found in the extrastriola.(ABSTRACT TRUNCATED AT 400 WORDS)
This article has been cited by other articles:
![]() |
A. Li, J. Xue, and E. H. Peterson Architecture of the Mouse Utricle: Macular Organization and Hair Bundle Heights J Neurophysiol, February 1, 2008; 99(2): 718 - 733. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. H. Rowe and E. H. Peterson Autocorrelation Analysis of Hair Bundle Structure in the Utricle J Neurophysiol, November 1, 2006; 96(5): 2653 - 2669. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zakir and J. D. Dickman Regeneration of vestibular otolith afferents after ototoxic damage. J. Neurosci., March 15, 2006; 26(11): 2881 - 2893. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Autret, I. Mechaly, F. Scamps, J. Valmier, P. Lory, and G. Desmadryl The involvement of Cav3.2/{alpha}1H T-type calcium channels in excitability of mouse embryonic primary vestibular neurones J. Physiol., August 15, 2005; 567(1): 67 - 78. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. M. Highstein, R. D. Rabbitt, G. R. Holstein, and R. D. Boyle Determinants of Spatial and Temporal Coding by Semicircular Canal Afferents J Neurophysiol, May 1, 2005; 93(5): 2359 - 2370. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. S. Desai, C. Zeh, and A. Lysakowski Comparative Morphology of Rodent Vestibular Periphery. I. Saccular and Utricular Maculae J Neurophysiol, January 1, 2005; 93(1): 251 - 266. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. S. Desai, H. Ali, and A. Lysakowski Comparative Morphology of Rodent Vestibular Periphery. II. Cristae Ampullares J Neurophysiol, January 1, 2005; 93(1): 267 - 280. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. C. Fitzpatrick and B. L. Day Probing the human vestibular system with galvanic stimulation J Appl Physiol, June 1, 2004; 96(6): 2301 - 2316. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Vollrath and R. A. Eatock Time Course and Extent of Mechanotransducer Adaptation in Mouse Utricular Hair Cells: Comparison With Frog Saccular Hair Cells J Neurophysiol, October 1, 2003; 90(4): 2676 - 2689. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Si, M. Md. Zakir, and J. D. Dickman Afferent Innervation of the Utricular Macula in Pigeons J Neurophysiol, March 1, 2003; 89(3): 1660 - 1677. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Zakir, D. Huss, and J. D. Dickman Afferent Innervation Patterns of the Saccule in Pigeons J Neurophysiol, January 1, 2003; 89(1): 534 - 550. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Rusch, A. Lysakowski, and R. A. Eatock Postnatal Development of Type I and Type II Hair Cells in the Mouse Utricle: Acquisition of Voltage-Gated Conductances and Differentiated Morphology J. Neurosci., September 15, 1998; 18(18): 7487 - 7501. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |