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Effects of Hyperthyroidism on the Rectus Muscles in Mice

Background: Structural details of vertebrate extraocular muscles (EOMs) have shown an anatomically and functionally distinct laminar organization into an outer orbital (OL) and an inner global layer (GL). Since hyperthyroidism alters tissue oxidative metabolism through mitochondrial enzymes, it is e...

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Autores principales: Nien, Chyong Jy, Jester, James V., Bose, Swaraj
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015165/
https://www.ncbi.nlm.nih.gov/pubmed/21212842
http://dx.doi.org/10.3389/fneur.2010.00143
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author Nien, Chyong Jy
Jester, James V.
Bose, Swaraj
author_facet Nien, Chyong Jy
Jester, James V.
Bose, Swaraj
author_sort Nien, Chyong Jy
collection PubMed
description Background: Structural details of vertebrate extraocular muscles (EOMs) have shown an anatomically and functionally distinct laminar organization into an outer orbital (OL) and an inner global layer (GL). Since hyperthyroidism alters tissue oxidative metabolism through mitochondrial enzymes, it is expected that structural/mitochondrial changes may be seen in hyperthyroid EOMs. We investigated the alterations in the laminar organization and mitochondrial changes in hyperthyroid mouse EOMs. Methods: Hyperthyroidism was induced in C57BL/6 mice and fresh rectus muscles were obtained to identify functional mitochondria using MitoTracker® Green and confocal microscopy; frozen sections from rectus muscles were stained with anti-rabbit Troponin T (selectively present in the OL) to demonstrate changes in the OL and GL of the EOMs. Ultrastructural features of EOMs were studied using transmission electron microscopy (TEM). Results: Of all four rectus EOMs studied, the maximum change was seen in the inferior rectus muscle (IR) followed by medial rectus (MR). Myofiber cross-sectional area measurements and Troponin T staining in the control IR EOMs demonstrated a smaller OL (113.2 ± 3.66 μm(2)) and higher density staining with Troponin T (90%) and a larger GL (411 ± 13.84 μm(2)) with low intensity staining (10%), while hyperthyroidism resulted in an increased OL (205.9 ± 5.3 μm(2)) and decreased GL (271.7 ± 7.5 μm(2)) p = 0.001. Confocal microscopy demonstrated an intense staining especially in the outer rims in the hyperthyroid IR which was confirmed by TEM showing structural alterations in the mitochondria and a subsarcolemmal migration. Conclusions: The outer, thinner, OL of the mouse EOM contains smaller diameter myofibers and fewer mitochondria while the inner, larger GL contains larger diameter myofibers and larger density of mitochondria. Hyperthyroidism results in a significant alteration in the laminar organization and mitochondrial alterations of mouse EOMs.
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spelling pubmed-30151652011-01-06 Effects of Hyperthyroidism on the Rectus Muscles in Mice Nien, Chyong Jy Jester, James V. Bose, Swaraj Front Neurol Neuroscience Background: Structural details of vertebrate extraocular muscles (EOMs) have shown an anatomically and functionally distinct laminar organization into an outer orbital (OL) and an inner global layer (GL). Since hyperthyroidism alters tissue oxidative metabolism through mitochondrial enzymes, it is expected that structural/mitochondrial changes may be seen in hyperthyroid EOMs. We investigated the alterations in the laminar organization and mitochondrial changes in hyperthyroid mouse EOMs. Methods: Hyperthyroidism was induced in C57BL/6 mice and fresh rectus muscles were obtained to identify functional mitochondria using MitoTracker® Green and confocal microscopy; frozen sections from rectus muscles were stained with anti-rabbit Troponin T (selectively present in the OL) to demonstrate changes in the OL and GL of the EOMs. Ultrastructural features of EOMs were studied using transmission electron microscopy (TEM). Results: Of all four rectus EOMs studied, the maximum change was seen in the inferior rectus muscle (IR) followed by medial rectus (MR). Myofiber cross-sectional area measurements and Troponin T staining in the control IR EOMs demonstrated a smaller OL (113.2 ± 3.66 μm(2)) and higher density staining with Troponin T (90%) and a larger GL (411 ± 13.84 μm(2)) with low intensity staining (10%), while hyperthyroidism resulted in an increased OL (205.9 ± 5.3 μm(2)) and decreased GL (271.7 ± 7.5 μm(2)) p = 0.001. Confocal microscopy demonstrated an intense staining especially in the outer rims in the hyperthyroid IR which was confirmed by TEM showing structural alterations in the mitochondria and a subsarcolemmal migration. Conclusions: The outer, thinner, OL of the mouse EOM contains smaller diameter myofibers and fewer mitochondria while the inner, larger GL contains larger diameter myofibers and larger density of mitochondria. Hyperthyroidism results in a significant alteration in the laminar organization and mitochondrial alterations of mouse EOMs. Frontiers Research Foundation 2010-11-11 /pmc/articles/PMC3015165/ /pubmed/21212842 http://dx.doi.org/10.3389/fneur.2010.00143 Text en Copyright © 2010 Nien, Jester and Bose. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Nien, Chyong Jy
Jester, James V.
Bose, Swaraj
Effects of Hyperthyroidism on the Rectus Muscles in Mice
title Effects of Hyperthyroidism on the Rectus Muscles in Mice
title_full Effects of Hyperthyroidism on the Rectus Muscles in Mice
title_fullStr Effects of Hyperthyroidism on the Rectus Muscles in Mice
title_full_unstemmed Effects of Hyperthyroidism on the Rectus Muscles in Mice
title_short Effects of Hyperthyroidism on the Rectus Muscles in Mice
title_sort effects of hyperthyroidism on the rectus muscles in mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015165/
https://www.ncbi.nlm.nih.gov/pubmed/21212842
http://dx.doi.org/10.3389/fneur.2010.00143
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