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Fiber counts and architecture of the human dorsal penile nerve

The human penis transmits behaviorally important sensory information via the dorsal penile nerve, which is required for initiation and maintenance of erection. The human penis differs from the penes of other hominids. The lack of a baculum makes the human penis dependent on erectile tissue, which is...

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Autores principales: Tunçkol, Elçin, Purkart, Leopold, Eigen, Lennart, Vida, Imre, Brecht, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232416/
https://www.ncbi.nlm.nih.gov/pubmed/37258532
http://dx.doi.org/10.1038/s41598-023-35030-w
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author Tunçkol, Elçin
Purkart, Leopold
Eigen, Lennart
Vida, Imre
Brecht, Michael
author_facet Tunçkol, Elçin
Purkart, Leopold
Eigen, Lennart
Vida, Imre
Brecht, Michael
author_sort Tunçkol, Elçin
collection PubMed
description The human penis transmits behaviorally important sensory information via the dorsal penile nerve, which is required for initiation and maintenance of erection. The human penis differs from the penes of other hominids. The lack of a baculum makes the human penis dependent on erectile tissue, which is under control of neural signals activated by tactile stimulation. Accordingly, the penile sensory innervation is crucial for human sexual behavior. To clarify penile innervation, we analyzed the architecture of the dorsal penile nerve of five male subjects who donated their body. We stained the sensory fibers in the penile dorsal nerve with anti-neurofilament H antibody, and identified myelinated axons with Luxol fast blue staining. Furthermore, we visualized nerve bundles as they travel along the shaft of the penis by performing microfocus computed tomography scans after counterstaining penes with iodine. Our results show that the dorsal penile nerve is organized in 25–45 loosely packed nerve bundles, running mediodorsally in the shaft of the penis. This organization corresponds to that in penes of other mammalian species, but differs from the organization of the other peripheral sensory nerves. Around half of the dorsal penile nerve fibers were myelinated and a human hemipenis contained a total of 8290 ± 2553 (mean ± SD) axons. Thus, the number of sensory axons in the human dorsal penile nerve is higher than in other species described so far. The large fraction of unmyelinated nerve fibers suggests that the conduction speed is not a crucial aspect of penile sensory transmission.
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spelling pubmed-102324162023-06-02 Fiber counts and architecture of the human dorsal penile nerve Tunçkol, Elçin Purkart, Leopold Eigen, Lennart Vida, Imre Brecht, Michael Sci Rep Article The human penis transmits behaviorally important sensory information via the dorsal penile nerve, which is required for initiation and maintenance of erection. The human penis differs from the penes of other hominids. The lack of a baculum makes the human penis dependent on erectile tissue, which is under control of neural signals activated by tactile stimulation. Accordingly, the penile sensory innervation is crucial for human sexual behavior. To clarify penile innervation, we analyzed the architecture of the dorsal penile nerve of five male subjects who donated their body. We stained the sensory fibers in the penile dorsal nerve with anti-neurofilament H antibody, and identified myelinated axons with Luxol fast blue staining. Furthermore, we visualized nerve bundles as they travel along the shaft of the penis by performing microfocus computed tomography scans after counterstaining penes with iodine. Our results show that the dorsal penile nerve is organized in 25–45 loosely packed nerve bundles, running mediodorsally in the shaft of the penis. This organization corresponds to that in penes of other mammalian species, but differs from the organization of the other peripheral sensory nerves. Around half of the dorsal penile nerve fibers were myelinated and a human hemipenis contained a total of 8290 ± 2553 (mean ± SD) axons. Thus, the number of sensory axons in the human dorsal penile nerve is higher than in other species described so far. The large fraction of unmyelinated nerve fibers suggests that the conduction speed is not a crucial aspect of penile sensory transmission. Nature Publishing Group UK 2023-05-31 /pmc/articles/PMC10232416/ /pubmed/37258532 http://dx.doi.org/10.1038/s41598-023-35030-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tunçkol, Elçin
Purkart, Leopold
Eigen, Lennart
Vida, Imre
Brecht, Michael
Fiber counts and architecture of the human dorsal penile nerve
title Fiber counts and architecture of the human dorsal penile nerve
title_full Fiber counts and architecture of the human dorsal penile nerve
title_fullStr Fiber counts and architecture of the human dorsal penile nerve
title_full_unstemmed Fiber counts and architecture of the human dorsal penile nerve
title_short Fiber counts and architecture of the human dorsal penile nerve
title_sort fiber counts and architecture of the human dorsal penile nerve
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232416/
https://www.ncbi.nlm.nih.gov/pubmed/37258532
http://dx.doi.org/10.1038/s41598-023-35030-w
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