Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons.
<h4>Background</h4>Our knowledge about the neural code in the auditory nerve is based to a large extent on experiments on cats. Several anatomical differences between auditory neurons in human and cat are expected to lead to functional differences in speed and safety of spike conduction....
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2013
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oai:doaj.org-article:6309a65bee6d4c8d8986b48fbeae7f082021-11-18T08:47:41ZImpact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons.1932-620310.1371/journal.pone.0079256https://doaj.org/article/6309a65bee6d4c8d8986b48fbeae7f082013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24260179/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Our knowledge about the neural code in the auditory nerve is based to a large extent on experiments on cats. Several anatomical differences between auditory neurons in human and cat are expected to lead to functional differences in speed and safety of spike conduction.<h4>Methodology/principal findings</h4>Confocal microscopy was used to systematically evaluate peripheral and central process diameters, commonness of myelination and morphology of spiral ganglion neurons (SGNs) along the cochlea of three human and three cats. Based on these morphometric data, model analysis reveales that spike conduction in SGNs is characterized by four phases: a postsynaptic delay, constant velocity in the peripheral process, a presomatic delay and constant velocity in the central process. The majority of SGNs are type I, connecting the inner hair cells with the brainstem. In contrast to those of humans, type I neurons of the cat are entirely myelinated. Biophysical model evaluation showed delayed and weak spikes in the human soma region as a consequence of a lack of myelin. The simulated spike conduction times are in accordance with normal interwave latencies from auditory brainstem response recordings from man and cat. Simulated 400 pA postsynaptic currents from inner hair cell ribbon synapses were 15 times above threshold. They enforced quick and synchronous spiking. Both of these properties were not present in type II cells as they receive fewer and much weaker (∼26 pA) synaptic stimuli.<h4>Conclusions/significance</h4>Wasting synaptic energy boosts spike initiation, which guarantees the rapid transmission of temporal fine structure of auditory signals. However, a lack of myelin in the soma regions of human type I neurons causes a large delay in spike conduction in comparison with cat neurons. The absent myelin, in combination with a longer peripheral process, causes quantitative differences of temporal parameters in the electrically stimulated human cochlea compared to the cat cochlea.Frank RattayThomas PotrusilCornelia WengerAndrew K WiseRudolf GlueckertAnneliese Schrott-FischerPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 11, p e79256 (2013) |
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Medicine R Science Q |
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Medicine R Science Q Frank Rattay Thomas Potrusil Cornelia Wenger Andrew K Wise Rudolf Glueckert Anneliese Schrott-Fischer Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| description |
<h4>Background</h4>Our knowledge about the neural code in the auditory nerve is based to a large extent on experiments on cats. Several anatomical differences between auditory neurons in human and cat are expected to lead to functional differences in speed and safety of spike conduction.<h4>Methodology/principal findings</h4>Confocal microscopy was used to systematically evaluate peripheral and central process diameters, commonness of myelination and morphology of spiral ganglion neurons (SGNs) along the cochlea of three human and three cats. Based on these morphometric data, model analysis reveales that spike conduction in SGNs is characterized by four phases: a postsynaptic delay, constant velocity in the peripheral process, a presomatic delay and constant velocity in the central process. The majority of SGNs are type I, connecting the inner hair cells with the brainstem. In contrast to those of humans, type I neurons of the cat are entirely myelinated. Biophysical model evaluation showed delayed and weak spikes in the human soma region as a consequence of a lack of myelin. The simulated spike conduction times are in accordance with normal interwave latencies from auditory brainstem response recordings from man and cat. Simulated 400 pA postsynaptic currents from inner hair cell ribbon synapses were 15 times above threshold. They enforced quick and synchronous spiking. Both of these properties were not present in type II cells as they receive fewer and much weaker (∼26 pA) synaptic stimuli.<h4>Conclusions/significance</h4>Wasting synaptic energy boosts spike initiation, which guarantees the rapid transmission of temporal fine structure of auditory signals. However, a lack of myelin in the soma regions of human type I neurons causes a large delay in spike conduction in comparison with cat neurons. The absent myelin, in combination with a longer peripheral process, causes quantitative differences of temporal parameters in the electrically stimulated human cochlea compared to the cat cochlea. |
| format |
article |
| author |
Frank Rattay Thomas Potrusil Cornelia Wenger Andrew K Wise Rudolf Glueckert Anneliese Schrott-Fischer |
| author_facet |
Frank Rattay Thomas Potrusil Cornelia Wenger Andrew K Wise Rudolf Glueckert Anneliese Schrott-Fischer |
| author_sort |
Frank Rattay |
| title |
Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| title_short |
Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| title_full |
Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| title_fullStr |
Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| title_full_unstemmed |
Impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| title_sort |
impact of morphometry, myelinization and synaptic current strength on spike conduction in human and cat spiral ganglion neurons. |
| publisher |
Public Library of Science (PLoS) |
| publishDate |
2013 |
| url |
https://doaj.org/article/6309a65bee6d4c8d8986b48fbeae7f08 |
| work_keys_str_mv |
AT frankrattay impactofmorphometrymyelinizationandsynapticcurrentstrengthonspikeconductioninhumanandcatspiralganglionneurons AT thomaspotrusil impactofmorphometrymyelinizationandsynapticcurrentstrengthonspikeconductioninhumanandcatspiralganglionneurons AT corneliawenger impactofmorphometrymyelinizationandsynapticcurrentstrengthonspikeconductioninhumanandcatspiralganglionneurons AT andrewkwise impactofmorphometrymyelinizationandsynapticcurrentstrengthonspikeconductioninhumanandcatspiralganglionneurons AT rudolfglueckert impactofmorphometrymyelinizationandsynapticcurrentstrengthonspikeconductioninhumanandcatspiralganglionneurons AT annelieseschrottfischer impactofmorphometrymyelinizationandsynapticcurrentstrengthonspikeconductioninhumanandcatspiralganglionneurons |
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