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Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels
We investigated cytosolic calcium (Ca(2+)) and sarcoplasmic reticulum Ca(2+) regulation in skeletal muscle fibers of hibernating Daurian ground squirrels (Spermophilus dauricus), non-hibernating hindlimb-unloaded (HLU) squirrels, and HLU rats to clarify the molecular mechanisms involved in preventin...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585226/ https://www.ncbi.nlm.nih.gov/pubmed/28874726 http://dx.doi.org/10.1038/s41598-017-10829-6 |
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author | Guo, Quanling Mi, Xin Sun, Xiaoyong Li, Xiaoyu Fu, Weiwei Xu, Shenhui Wang, Qi Arfat, Yasir Wang, Huiping Chang, Hui Gao, Yunfang |
author_facet | Guo, Quanling Mi, Xin Sun, Xiaoyong Li, Xiaoyu Fu, Weiwei Xu, Shenhui Wang, Qi Arfat, Yasir Wang, Huiping Chang, Hui Gao, Yunfang |
author_sort | Guo, Quanling |
collection | PubMed |
description | We investigated cytosolic calcium (Ca(2+)) and sarcoplasmic reticulum Ca(2+) regulation in skeletal muscle fibers of hibernating Daurian ground squirrels (Spermophilus dauricus), non-hibernating hindlimb-unloaded (HLU) squirrels, and HLU rats to clarify the molecular mechanisms involved in preventing muscle atrophy in hibernators. The Na(+), K(+)-ATPase and Ca(2+)-ATPase activities in the soleus muscle (SOL) of squirrels were maintained in hibernation, decreased during interbout arousal (IB-A), and increased to autumn/pre-hibernation (AUT/Pre-H) levels in torpor after interbout arousal (Post-IBA), whereas activities in the extensor digitorum longus muscle (EDL) were stable during hibernation, but increased during post-hibernation (Post-H). Activities increased in the SOL of HLU rats, but were stable in HLU squirrels. Sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) activity in the SOL decreased in IB-A squirrels, but returned to AUT/Pre-H levels in the Post-IBA group; no significant changes were found in the EDL. SERCA activity increased in the EDL of HLU squirrels and SOL of HLU rats. Compared with AUT/Pre-H, SERCA type 2 protein expression increased in the SOL and EDL of IB-A and Post-IBA squirrels, but increased in the SOL only in HLU animals. We also describe the protein kinase A changes in this paper. Thus, hibernating ground squirrels displayed remarkable Na(+), K(+)-ATPase, Ca(2+)-ATPase, and SERCA plasticity. |
format | Online Article Text |
id | pubmed-5585226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55852262017-09-06 Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels Guo, Quanling Mi, Xin Sun, Xiaoyong Li, Xiaoyu Fu, Weiwei Xu, Shenhui Wang, Qi Arfat, Yasir Wang, Huiping Chang, Hui Gao, Yunfang Sci Rep Article We investigated cytosolic calcium (Ca(2+)) and sarcoplasmic reticulum Ca(2+) regulation in skeletal muscle fibers of hibernating Daurian ground squirrels (Spermophilus dauricus), non-hibernating hindlimb-unloaded (HLU) squirrels, and HLU rats to clarify the molecular mechanisms involved in preventing muscle atrophy in hibernators. The Na(+), K(+)-ATPase and Ca(2+)-ATPase activities in the soleus muscle (SOL) of squirrels were maintained in hibernation, decreased during interbout arousal (IB-A), and increased to autumn/pre-hibernation (AUT/Pre-H) levels in torpor after interbout arousal (Post-IBA), whereas activities in the extensor digitorum longus muscle (EDL) were stable during hibernation, but increased during post-hibernation (Post-H). Activities increased in the SOL of HLU rats, but were stable in HLU squirrels. Sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) activity in the SOL decreased in IB-A squirrels, but returned to AUT/Pre-H levels in the Post-IBA group; no significant changes were found in the EDL. SERCA activity increased in the EDL of HLU squirrels and SOL of HLU rats. Compared with AUT/Pre-H, SERCA type 2 protein expression increased in the SOL and EDL of IB-A and Post-IBA squirrels, but increased in the SOL only in HLU animals. We also describe the protein kinase A changes in this paper. Thus, hibernating ground squirrels displayed remarkable Na(+), K(+)-ATPase, Ca(2+)-ATPase, and SERCA plasticity. Nature Publishing Group UK 2017-09-05 /pmc/articles/PMC5585226/ /pubmed/28874726 http://dx.doi.org/10.1038/s41598-017-10829-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guo, Quanling Mi, Xin Sun, Xiaoyong Li, Xiaoyu Fu, Weiwei Xu, Shenhui Wang, Qi Arfat, Yasir Wang, Huiping Chang, Hui Gao, Yunfang Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels |
title | Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels |
title_full | Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels |
title_fullStr | Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels |
title_full_unstemmed | Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels |
title_short | Remarkable plasticity of Na(+), K(+)-ATPase, Ca(2+)-ATPase and SERCA contributes to muscle disuse atrophy resistance in hibernating Daurian ground squirrels |
title_sort | remarkable plasticity of na(+), k(+)-atpase, ca(2+)-atpase and serca contributes to muscle disuse atrophy resistance in hibernating daurian ground squirrels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5585226/ https://www.ncbi.nlm.nih.gov/pubmed/28874726 http://dx.doi.org/10.1038/s41598-017-10829-6 |
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