Innervation Densities of Inner and Outer Hair Cells of the Human Organ of Corti

ORL ◽  
1988 ◽  
Vol 50 (6) ◽  
pp. 363-370 ◽  
Author(s):  
Joseph B. Nadol, Jr.
1983 ◽  
Vol 76 (4) ◽  
pp. 269-278 ◽  
Author(s):  
A Wright

The human cochlea has been preserved from post-mortem autolysis by perfusion with a fixative shortly after death. Subsequent staining with osmium permits dissection of this structure from the temporal bone. (Temporal bones were obtained from eight patients). When prepared for examination in the scanning electron microscope, the auditory sensory cells are found to be located in the band-like organ of Corti which extends the length of the cochlea. The sensory cells have a cluster of stereocilia projecting from their free upper surface and because of this are called hair cells. The hair cells are divided into two separate groups: a single row of inner hair cells, which show little variation in their surface appearance along the length of the cochlea, and three or four rows of outer hair cells whose cilia change in conformation and increase in length along the cochlea.


1981 ◽  
Vol 90 (1) ◽  
pp. 12-17 ◽  
Author(s):  
Joseph B. Nadol

Reciprocal synapses have been found between nerve terminals and the outer hair cells in the human organ of Corti. A single nerve ending of the nonvesiculated type may possess two types of synaptic specialization of opposite polarity. The first is typical of the “afferent” synapse with a presynaptic body in the hair cell and pre- and postsynaptic membrane thickening. The second consists of a small collection of presynaptic vesicles in the neural cytoplasm near the plasma membrane facing the hair cell and a subsynaptic cisterna within the hair cell cytoplasm. The second type of specialization is similar to the synapses seen in “efferent” endings. This suggests that both an afferent (hair cell to neuron) and efferent (neuron to hair cell) synaptic relationship may exist between an outer hair cell and a single nerve terminal.


1999 ◽  
Vol 27 (2) ◽  
pp. 73-77 ◽  
Author(s):  
Miguel A. Lopez-Gonzalez ◽  
Juan M. Guerrero ◽  
Francisco Rojas ◽  
Carmen Osuna ◽  
Francisco Delgado

1978 ◽  
Vol 26 (4) ◽  
pp. 313-317 ◽  
Author(s):  
T Omata ◽  
I Ohtani ◽  
K Ohtsuki ◽  
J Ouchi

A method for the detection of lactic dehydrogenase enzymatic activity in outer hair cells of the rabbit is described. The membranous labyrinth with temporal bone was prefixed in glutaraldehyde. After being placed into the incubation medium, it was postfixed in osmium tetroxide. Specimens of the organ of Corti were removed. Then the specimens were embedded in water-soluble glycol and cut with a cryostat for light microscopy, and also they were embedded in Epon and cut for light and electron microscopy. Sectioning of the membranous labyrinth was very easily made when the specimens were embedded in both the water-soluble glycol and the Epon. The structures of the frozen sections as well as the Epon-embedded ones were well preserved. In the frozen sections the preservation and localization of reaction products were thoroughly kept, but monoformazan of the Epon-embedded sections was soluble.


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