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Signature molecular changes in the skeletal muscle of hindlimb unloaded mice

Hind-limb unloaded (HU) mouse is a well-recognized model of muscle atrophy; however, the molecular changes in the skeletal muscle during unloading are poorly characterized. We have used Raman spectroscopy to evaluate the structure and behavior of signature molecules involved in regulating muscle str...

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Detalles Bibliográficos
Autores principales: Azeem, Muhammad, Qaisar, Rizwan, Karim, Asima, Ranade, Anu, Elmoselhi, Adel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851774/
https://www.ncbi.nlm.nih.gov/pubmed/33553690
http://dx.doi.org/10.1016/j.bbrep.2021.100930
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author Azeem, Muhammad
Qaisar, Rizwan
Karim, Asima
Ranade, Anu
Elmoselhi, Adel
author_facet Azeem, Muhammad
Qaisar, Rizwan
Karim, Asima
Ranade, Anu
Elmoselhi, Adel
author_sort Azeem, Muhammad
collection PubMed
description Hind-limb unloaded (HU) mouse is a well-recognized model of muscle atrophy; however, the molecular changes in the skeletal muscle during unloading are poorly characterized. We have used Raman spectroscopy to evaluate the structure and behavior of signature molecules involved in regulating muscle structural and functional health. The Raman spectroscopic analysis of gastrocnemius muscles was compared between 16-18 weeks old HU c57Bl/6J mice and ground-based controls. The spectra showed that the signals for asparagine and glutamine were reduced in HU mice, possibly indicating increased catabolism. The peaks for hydroxyproline and proline were split, pointing towards molecular breakdown and reduced tendon repair. We also report a consistently increased intensity in> 1300 cm(-1) range in the Raman spectra along with a shift towards higher frequencies in the HU mice, indicating activation of sarcoplasmic reticulum (SR) stress during HU.
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spelling pubmed-78517742021-02-05 Signature molecular changes in the skeletal muscle of hindlimb unloaded mice Azeem, Muhammad Qaisar, Rizwan Karim, Asima Ranade, Anu Elmoselhi, Adel Biochem Biophys Rep Research Article Hind-limb unloaded (HU) mouse is a well-recognized model of muscle atrophy; however, the molecular changes in the skeletal muscle during unloading are poorly characterized. We have used Raman spectroscopy to evaluate the structure and behavior of signature molecules involved in regulating muscle structural and functional health. The Raman spectroscopic analysis of gastrocnemius muscles was compared between 16-18 weeks old HU c57Bl/6J mice and ground-based controls. The spectra showed that the signals for asparagine and glutamine were reduced in HU mice, possibly indicating increased catabolism. The peaks for hydroxyproline and proline were split, pointing towards molecular breakdown and reduced tendon repair. We also report a consistently increased intensity in> 1300 cm(-1) range in the Raman spectra along with a shift towards higher frequencies in the HU mice, indicating activation of sarcoplasmic reticulum (SR) stress during HU. Elsevier 2021-01-29 /pmc/articles/PMC7851774/ /pubmed/33553690 http://dx.doi.org/10.1016/j.bbrep.2021.100930 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Azeem, Muhammad
Qaisar, Rizwan
Karim, Asima
Ranade, Anu
Elmoselhi, Adel
Signature molecular changes in the skeletal muscle of hindlimb unloaded mice
title Signature molecular changes in the skeletal muscle of hindlimb unloaded mice
title_full Signature molecular changes in the skeletal muscle of hindlimb unloaded mice
title_fullStr Signature molecular changes in the skeletal muscle of hindlimb unloaded mice
title_full_unstemmed Signature molecular changes in the skeletal muscle of hindlimb unloaded mice
title_short Signature molecular changes in the skeletal muscle of hindlimb unloaded mice
title_sort signature molecular changes in the skeletal muscle of hindlimb unloaded mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851774/
https://www.ncbi.nlm.nih.gov/pubmed/33553690
http://dx.doi.org/10.1016/j.bbrep.2021.100930
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