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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...

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Autores principales: Guo, Quanling, Mi, Xin, Sun, Xiaoyong, Li, Xiaoyu, Fu, Weiwei, Xu, Shenhui, Wang, Qi, Arfat, Yasir, Wang, Huiping, Chang, Hui, Gao, Yunfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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