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Multiparity affects conduction properties of pelvic floor nerves in rabbits
INTRODUCTION: Women often develop pelvic floor dysfunction due to damage to the pelvic musculature during childbirth; however, the effect on pelvic floor nerves function is less understood. This study used adult rabbits to evaluate the electrophysiological and histological characteristics of the bul...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192397/ https://www.ncbi.nlm.nih.gov/pubmed/30240150 http://dx.doi.org/10.1002/brb3.1105 |
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author | Castelán, Francisco López‐García, Kenia Moreno‐Pérez, Suelem Zempoalteca, René Corona‐Quintanilla, Dora L. Romero‐Ortega, Mario I. Jiménez‐Estrada, Ismael Martínez‐Gómez, Margarita |
author_facet | Castelán, Francisco López‐García, Kenia Moreno‐Pérez, Suelem Zempoalteca, René Corona‐Quintanilla, Dora L. Romero‐Ortega, Mario I. Jiménez‐Estrada, Ismael Martínez‐Gómez, Margarita |
author_sort | Castelán, Francisco |
collection | PubMed |
description | INTRODUCTION: Women often develop pelvic floor dysfunction due to damage to the pelvic musculature during childbirth; however, the effect on pelvic floor nerves function is less understood. This study used adult rabbits to evaluate the electrophysiological and histological characteristics of the bulbospongiosus (Bsn) and pubococcygeus nerves (Pcn) in multiparity. METHODS: Compound nerve action potentials (CNAP) were compared between age‐matched nulliparous and multiparous animals and associated to the histological characteristics of myelinated axons from the Bsn and Pcn nerves. The extensor digitorum longus nerve (EDLn) was used as negative control. Data were analyzed with unpaired two‐tailed Student's t test or Mann–Whitney U test to determine significant differences between groups. RESULTS: The onset and peak latencies, duration, and conduction velocity of the motor fibers in these pelvic nerves were not significantly different between nulliparous and multiparous animals. However, the peak‐to‐peak amplitude and area of the CNAP in both Bsn and Pcn were reduced in multiparous rabbits. Histology showed a higher percentage of axons with myelin disorganization caused by multiparity in these pelvic nerves. Together, the data indicate a reduction in the number of functional pelvic axons due to multiparity. As expected, no effect of parity was observed in the EDLn controls. CONCLUSIONS: Present findings demonstrated that multiparity affects myelination and consequently conduction properties in the small pelvic floor nerves. |
format | Online Article Text |
id | pubmed-6192397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61923972018-10-22 Multiparity affects conduction properties of pelvic floor nerves in rabbits Castelán, Francisco López‐García, Kenia Moreno‐Pérez, Suelem Zempoalteca, René Corona‐Quintanilla, Dora L. Romero‐Ortega, Mario I. Jiménez‐Estrada, Ismael Martínez‐Gómez, Margarita Brain Behav Original Research INTRODUCTION: Women often develop pelvic floor dysfunction due to damage to the pelvic musculature during childbirth; however, the effect on pelvic floor nerves function is less understood. This study used adult rabbits to evaluate the electrophysiological and histological characteristics of the bulbospongiosus (Bsn) and pubococcygeus nerves (Pcn) in multiparity. METHODS: Compound nerve action potentials (CNAP) were compared between age‐matched nulliparous and multiparous animals and associated to the histological characteristics of myelinated axons from the Bsn and Pcn nerves. The extensor digitorum longus nerve (EDLn) was used as negative control. Data were analyzed with unpaired two‐tailed Student's t test or Mann–Whitney U test to determine significant differences between groups. RESULTS: The onset and peak latencies, duration, and conduction velocity of the motor fibers in these pelvic nerves were not significantly different between nulliparous and multiparous animals. However, the peak‐to‐peak amplitude and area of the CNAP in both Bsn and Pcn were reduced in multiparous rabbits. Histology showed a higher percentage of axons with myelin disorganization caused by multiparity in these pelvic nerves. Together, the data indicate a reduction in the number of functional pelvic axons due to multiparity. As expected, no effect of parity was observed in the EDLn controls. CONCLUSIONS: Present findings demonstrated that multiparity affects myelination and consequently conduction properties in the small pelvic floor nerves. John Wiley and Sons Inc. 2018-09-21 /pmc/articles/PMC6192397/ /pubmed/30240150 http://dx.doi.org/10.1002/brb3.1105 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Castelán, Francisco López‐García, Kenia Moreno‐Pérez, Suelem Zempoalteca, René Corona‐Quintanilla, Dora L. Romero‐Ortega, Mario I. Jiménez‐Estrada, Ismael Martínez‐Gómez, Margarita Multiparity affects conduction properties of pelvic floor nerves in rabbits |
title | Multiparity affects conduction properties of pelvic floor nerves in rabbits |
title_full | Multiparity affects conduction properties of pelvic floor nerves in rabbits |
title_fullStr | Multiparity affects conduction properties of pelvic floor nerves in rabbits |
title_full_unstemmed | Multiparity affects conduction properties of pelvic floor nerves in rabbits |
title_short | Multiparity affects conduction properties of pelvic floor nerves in rabbits |
title_sort | multiparity affects conduction properties of pelvic floor nerves in rabbits |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192397/ https://www.ncbi.nlm.nih.gov/pubmed/30240150 http://dx.doi.org/10.1002/brb3.1105 |
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