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Intertubular morphometric and ultrastructural testes analyses in mdx mice

Duchenne Muscular Dystrophy (DMD) reproductive alterations and the influence of antioxidant treatments may aid in understanding morphometry testicular quantification. In this context, the aim of the present study was to characterize the intertubular compartment (ITC) morphometry of animal testes in...

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Autores principales: Braz, Janine Karla França da Silva, Gomes, Vilessa Araújo, Siman, Verônica Andrade, da Matta, Sérgio Luís Pinto, Clebis, Naianne Kelly, de Oliveira, Moacir Franco, Assis, Antônio Chaves, Morais, Danielle Barbosa, de Moura, Carlos Eduardo Bezerra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Colégio Brasileiro de Reprodução Animal 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613355/
https://www.ncbi.nlm.nih.gov/pubmed/36313597
http://dx.doi.org/10.1590/1984-3143-AR2021-0124
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author Braz, Janine Karla França da Silva
Gomes, Vilessa Araújo
Siman, Verônica Andrade
da Matta, Sérgio Luís Pinto
Clebis, Naianne Kelly
de Oliveira, Moacir Franco
Assis, Antônio Chaves
Morais, Danielle Barbosa
de Moura, Carlos Eduardo Bezerra
author_facet Braz, Janine Karla França da Silva
Gomes, Vilessa Araújo
Siman, Verônica Andrade
da Matta, Sérgio Luís Pinto
Clebis, Naianne Kelly
de Oliveira, Moacir Franco
Assis, Antônio Chaves
Morais, Danielle Barbosa
de Moura, Carlos Eduardo Bezerra
author_sort Braz, Janine Karla França da Silva
collection PubMed
description Duchenne Muscular Dystrophy (DMD) reproductive alterations and the influence of antioxidant treatments may aid in understanding morphometry testicular quantification. In this context, the aim of the present study was to characterize the intertubular compartment (ITC) morphometry of animal testes in mdx mice supplemented with ascorbic acid (AA). Sixteen mice were used, namely the C57BL/10 (non-dystrophic) and C57BL/10Mdx (dystrophic) lineages, distributed into the following groups: Control (C60), Dystrophic (D60), Control supplemented with AA (CS60), Dystrophic supplemented with AA (DS60). A total of 200 mg/kg of AA were administered to mice for 30 days. Subsequently, the testicles were collected, weighed, and fragmented. The obtained fragments were fixed in Karnovsky's solution (pH 7.2) and embedded in historesin for morphometric and transmission electron microscopy assessments. Leydig cells were hypertrophic in the D60 group, but was reverted by AA supplementation in the DS60 group. The DS60 group also exhibited increased intertubular volume compared to the CS60 group. The ultrastructural images identified multilamellar bodies in dystrophic animals (lipid storage) and telocyte cells (transport substances) in both control and dystrophic animals. Morphometric alterations were, therefore, noted in the intertubular compartment due to Duchenne muscular dystrophy (DMD), with AA administration capable of altering Leydig cells in this condition.
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spelling pubmed-96133552022-10-29 Intertubular morphometric and ultrastructural testes analyses in mdx mice Braz, Janine Karla França da Silva Gomes, Vilessa Araújo Siman, Verônica Andrade da Matta, Sérgio Luís Pinto Clebis, Naianne Kelly de Oliveira, Moacir Franco Assis, Antônio Chaves Morais, Danielle Barbosa de Moura, Carlos Eduardo Bezerra Anim Reprod Original Article Duchenne Muscular Dystrophy (DMD) reproductive alterations and the influence of antioxidant treatments may aid in understanding morphometry testicular quantification. In this context, the aim of the present study was to characterize the intertubular compartment (ITC) morphometry of animal testes in mdx mice supplemented with ascorbic acid (AA). Sixteen mice were used, namely the C57BL/10 (non-dystrophic) and C57BL/10Mdx (dystrophic) lineages, distributed into the following groups: Control (C60), Dystrophic (D60), Control supplemented with AA (CS60), Dystrophic supplemented with AA (DS60). A total of 200 mg/kg of AA were administered to mice for 30 days. Subsequently, the testicles were collected, weighed, and fragmented. The obtained fragments were fixed in Karnovsky's solution (pH 7.2) and embedded in historesin for morphometric and transmission electron microscopy assessments. Leydig cells were hypertrophic in the D60 group, but was reverted by AA supplementation in the DS60 group. The DS60 group also exhibited increased intertubular volume compared to the CS60 group. The ultrastructural images identified multilamellar bodies in dystrophic animals (lipid storage) and telocyte cells (transport substances) in both control and dystrophic animals. Morphometric alterations were, therefore, noted in the intertubular compartment due to Duchenne muscular dystrophy (DMD), with AA administration capable of altering Leydig cells in this condition. Colégio Brasileiro de Reprodução Animal 2022-10-24 /pmc/articles/PMC9613355/ /pubmed/36313597 http://dx.doi.org/10.1590/1984-3143-AR2021-0124 Text en https://creativecommons.org/licenses/by/4.0/Copyright © The Author(s). 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 work is properly cited.
spellingShingle Original Article
Braz, Janine Karla França da Silva
Gomes, Vilessa Araújo
Siman, Verônica Andrade
da Matta, Sérgio Luís Pinto
Clebis, Naianne Kelly
de Oliveira, Moacir Franco
Assis, Antônio Chaves
Morais, Danielle Barbosa
de Moura, Carlos Eduardo Bezerra
Intertubular morphometric and ultrastructural testes analyses in mdx mice
title Intertubular morphometric and ultrastructural testes analyses in mdx mice
title_full Intertubular morphometric and ultrastructural testes analyses in mdx mice
title_fullStr Intertubular morphometric and ultrastructural testes analyses in mdx mice
title_full_unstemmed Intertubular morphometric and ultrastructural testes analyses in mdx mice
title_short Intertubular morphometric and ultrastructural testes analyses in mdx mice
title_sort intertubular morphometric and ultrastructural testes analyses in mdx mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613355/
https://www.ncbi.nlm.nih.gov/pubmed/36313597
http://dx.doi.org/10.1590/1984-3143-AR2021-0124
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