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The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages

Pigs are models in human phoniatry. However, features of maturation and ageing have not been considered with regard to the so-called body-cover model in this species. Therefore, the glottis of “young” (2–3 months; n = 6) and “old” (4–7 years; n = 6) minipigs was investigated. Their cranial (CraF) an...

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Autores principales: Lang, Anja, Koch, Rüdiger, Rohn, Karl, Gasse, Hagen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446030/
https://www.ncbi.nlm.nih.gov/pubmed/26018404
http://dx.doi.org/10.1371/journal.pone.0128085
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author Lang, Anja
Koch, Rüdiger
Rohn, Karl
Gasse, Hagen
author_facet Lang, Anja
Koch, Rüdiger
Rohn, Karl
Gasse, Hagen
author_sort Lang, Anja
collection PubMed
description Pigs are models in human phoniatry. However, features of maturation and ageing have not been considered with regard to the so-called body-cover model in this species. Therefore, the glottis of “young” (2–3 months; n = 6) and “old” (4–7 years; n = 6) minipigs was investigated. Their cranial (CraF) and caudal (CauF) vocal folds were histomorphometrically and stratigraphically analysed with emphasis on their amounts of collagen structures and elastic fibres. A dense subepithelial layer (SEL) was a distinct feature of CraF and CauF of both age groups; it was spread upon the underlying loose, flexible “cover” like a fibro-elastic membrane. The “cover” was characterised by the so-called superficial layer (SL), which was distinctly loose in the “young” minipigs, but had a much denser texture in the “old” minipigs. Here, the SL was dominated by elastic fibres in the CraF, but was of mixed qualities (collagenous and elastic) in the CauF. The structural requirements for the SL’s function as a loose “cover” were thus met only in the “young” animals. A clearly demarcated intermediate layer (IL)—characterised by high amounts of elastic fibres (as in humans)—was only found in the CraF of the “young” animals. In the “old” animals, it had lost its demarcation. In the depth of the CraF of the “old” animals, many thick collagen fibre bundles were detected in a location equivalent to that of the vocal muscle in the CauF. The development of their large diameters was interpreted as part of the maturation process, thereby supporting the hypothesis of their functional importance as a component of the “body.” In the CauF, the amounts of collagen structures increased throughout the entire lamina propria, resulting in a loss of demarcated stratigraphical subdivisions in the “old” minipigs. This situation resembled that described in the vocal fold of geriatric humans.
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spelling pubmed-44460302015-06-09 The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages Lang, Anja Koch, Rüdiger Rohn, Karl Gasse, Hagen PLoS One Research Article Pigs are models in human phoniatry. However, features of maturation and ageing have not been considered with regard to the so-called body-cover model in this species. Therefore, the glottis of “young” (2–3 months; n = 6) and “old” (4–7 years; n = 6) minipigs was investigated. Their cranial (CraF) and caudal (CauF) vocal folds were histomorphometrically and stratigraphically analysed with emphasis on their amounts of collagen structures and elastic fibres. A dense subepithelial layer (SEL) was a distinct feature of CraF and CauF of both age groups; it was spread upon the underlying loose, flexible “cover” like a fibro-elastic membrane. The “cover” was characterised by the so-called superficial layer (SL), which was distinctly loose in the “young” minipigs, but had a much denser texture in the “old” minipigs. Here, the SL was dominated by elastic fibres in the CraF, but was of mixed qualities (collagenous and elastic) in the CauF. The structural requirements for the SL’s function as a loose “cover” were thus met only in the “young” animals. A clearly demarcated intermediate layer (IL)—characterised by high amounts of elastic fibres (as in humans)—was only found in the CraF of the “young” animals. In the “old” animals, it had lost its demarcation. In the depth of the CraF of the “old” animals, many thick collagen fibre bundles were detected in a location equivalent to that of the vocal muscle in the CauF. The development of their large diameters was interpreted as part of the maturation process, thereby supporting the hypothesis of their functional importance as a component of the “body.” In the CauF, the amounts of collagen structures increased throughout the entire lamina propria, resulting in a loss of demarcated stratigraphical subdivisions in the “old” minipigs. This situation resembled that described in the vocal fold of geriatric humans. Public Library of Science 2015-05-27 /pmc/articles/PMC4446030/ /pubmed/26018404 http://dx.doi.org/10.1371/journal.pone.0128085 Text en © 2015 Lang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lang, Anja
Koch, Rüdiger
Rohn, Karl
Gasse, Hagen
The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages
title The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages
title_full The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages
title_fullStr The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages
title_full_unstemmed The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages
title_short The Histological Components of the Phoniatrical Body-Cover Model in Minipigs of Different Ages
title_sort histological components of the phoniatrical body-cover model in minipigs of different ages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446030/
https://www.ncbi.nlm.nih.gov/pubmed/26018404
http://dx.doi.org/10.1371/journal.pone.0128085
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