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Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation

The unique, unmyelinated perikarya of spiral ganglion cells (SGCs) in the human cochlea are often arranged in functional units covered by common satellite glial cells. This micro anatomical peculiarity presents a crucial barrier for an action potential (AP) travelling from the sensory receptors to t...

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Autores principales: Potrusil, T., Wenger, C., Glueckert, R., Schrott-Fischer, A., Rattay, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377987/
https://www.ncbi.nlm.nih.gov/pubmed/22516012
http://dx.doi.org/10.1016/j.neuroscience.2012.03.033
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author Potrusil, T.
Wenger, C.
Glueckert, R.
Schrott-Fischer, A.
Rattay, F.
author_facet Potrusil, T.
Wenger, C.
Glueckert, R.
Schrott-Fischer, A.
Rattay, F.
author_sort Potrusil, T.
collection PubMed
description The unique, unmyelinated perikarya of spiral ganglion cells (SGCs) in the human cochlea are often arranged in functional units covered by common satellite glial cells. This micro anatomical peculiarity presents a crucial barrier for an action potential (AP) travelling from the sensory receptors to the brain. Confocal microscopy was used to acquire systematically volumetric data on perikarya and corresponding nuclei in their full dimension along the cochlea of two individuals. Four populations of SGCs within the human inner ear of two different specimens were identified using agglomerative hierarchical clustering, contrary to the present distinction of two groups of SGCs. Furthermore, we found evidence of a spatial arrangement of perikarya and their accordant nuclei along the cochlea spiral. In this arrangement, the most uniform sizes of cell bodies are located in the middle turn, which represents the majority of phonational frequencies. Since single-cell recordings from other mammalians may not be representative to humans and human SGCs are not accessible for physiological measurements, computer simulation has been used to quantify the effect of varying soma size on single neuron response to electrical micro stimulation. Results show that temporal parameters of the spiking pattern are affected by the size of the cell body. Cathodic stimulation was found to induce stronger variations of spikes while also leading to the lowest thresholds and longest latencies. Therefore, anodic stimulation leads to a more uniform excitation profile among SGCs with different cell body size.
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spelling pubmed-33779872012-07-12 Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation Potrusil, T. Wenger, C. Glueckert, R. Schrott-Fischer, A. Rattay, F. Neuroscience Article The unique, unmyelinated perikarya of spiral ganglion cells (SGCs) in the human cochlea are often arranged in functional units covered by common satellite glial cells. This micro anatomical peculiarity presents a crucial barrier for an action potential (AP) travelling from the sensory receptors to the brain. Confocal microscopy was used to acquire systematically volumetric data on perikarya and corresponding nuclei in their full dimension along the cochlea of two individuals. Four populations of SGCs within the human inner ear of two different specimens were identified using agglomerative hierarchical clustering, contrary to the present distinction of two groups of SGCs. Furthermore, we found evidence of a spatial arrangement of perikarya and their accordant nuclei along the cochlea spiral. In this arrangement, the most uniform sizes of cell bodies are located in the middle turn, which represents the majority of phonational frequencies. Since single-cell recordings from other mammalians may not be representative to humans and human SGCs are not accessible for physiological measurements, computer simulation has been used to quantify the effect of varying soma size on single neuron response to electrical micro stimulation. Results show that temporal parameters of the spiking pattern are affected by the size of the cell body. Cathodic stimulation was found to induce stronger variations of spikes while also leading to the lowest thresholds and longest latencies. Therefore, anodic stimulation leads to a more uniform excitation profile among SGCs with different cell body size. Elsevier Science 2012-07-12 /pmc/articles/PMC3377987/ /pubmed/22516012 http://dx.doi.org/10.1016/j.neuroscience.2012.03.033 Text en © 2012 Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Potrusil, T.
Wenger, C.
Glueckert, R.
Schrott-Fischer, A.
Rattay, F.
Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation
title Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation
title_full Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation
title_fullStr Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation
title_full_unstemmed Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation
title_short Morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: Consequences for single fiber response to electrical stimulation
title_sort morphometric classification and spatial organization of spiral ganglion neurons in the human cochlea: consequences for single fiber response to electrical stimulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377987/
https://www.ncbi.nlm.nih.gov/pubmed/22516012
http://dx.doi.org/10.1016/j.neuroscience.2012.03.033
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