Cargando…
Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state
PURPOSE: This review provides a current perspective on the mechanism of vitamin D on skeletal muscle function with the emphasis on oxidative stress, muscle anabolic state and muscle energy metabolism. It focuses on several aspects related to cellular and molecular physiology such as VDR as the trigg...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422984/ https://www.ncbi.nlm.nih.gov/pubmed/30830277 http://dx.doi.org/10.1007/s00421-019-04104-x |
_version_ | 1783404455151009792 |
---|---|
author | Dzik, Katarzyna Patrycja Kaczor, Jan Jacek |
author_facet | Dzik, Katarzyna Patrycja Kaczor, Jan Jacek |
author_sort | Dzik, Katarzyna Patrycja |
collection | PubMed |
description | PURPOSE: This review provides a current perspective on the mechanism of vitamin D on skeletal muscle function with the emphasis on oxidative stress, muscle anabolic state and muscle energy metabolism. It focuses on several aspects related to cellular and molecular physiology such as VDR as the trigger point of vitamin D action, oxidative stress as a consequence of vitamin D deficiency. METHOD: The interaction between vitamin D deficiency and mitochondrial function as well as skeletal muscle atrophy signalling pathways have been studied and clarified in the last years. To the best of our knowledge, we summarize key knowledge and knowledge gaps regarding the mechanism(s) of action of vitamin D in skeletal muscle. RESULT: Vitamin D deficiency is associated with oxidative stress in skeletal muscle that influences the mitochondrial function and affects the development of skeletal muscle atrophy. Namely, vitamin D deficiency decreases oxygen consumption rate and induces disruption of mitochondrial function. These deleterious consequences on muscle may be associated through the vitamin D receptor (VDR) action. Moreover, vitamin D deficiency may contribute to the development of muscle atrophy. The possible signalling pathway triggering the expression of Atrogin-1 involves Src-ERK1/2-Akt- FOXO causing protein degradation. CONCLUSION: Based on the current knowledge we propose that vitamin D deficiency results from the loss of VDR function and it could be partly responsible for the development of neurodegenerative diseases in human beings. |
format | Online Article Text |
id | pubmed-6422984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-64229842019-04-05 Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state Dzik, Katarzyna Patrycja Kaczor, Jan Jacek Eur J Appl Physiol Invited Review PURPOSE: This review provides a current perspective on the mechanism of vitamin D on skeletal muscle function with the emphasis on oxidative stress, muscle anabolic state and muscle energy metabolism. It focuses on several aspects related to cellular and molecular physiology such as VDR as the trigger point of vitamin D action, oxidative stress as a consequence of vitamin D deficiency. METHOD: The interaction between vitamin D deficiency and mitochondrial function as well as skeletal muscle atrophy signalling pathways have been studied and clarified in the last years. To the best of our knowledge, we summarize key knowledge and knowledge gaps regarding the mechanism(s) of action of vitamin D in skeletal muscle. RESULT: Vitamin D deficiency is associated with oxidative stress in skeletal muscle that influences the mitochondrial function and affects the development of skeletal muscle atrophy. Namely, vitamin D deficiency decreases oxygen consumption rate and induces disruption of mitochondrial function. These deleterious consequences on muscle may be associated through the vitamin D receptor (VDR) action. Moreover, vitamin D deficiency may contribute to the development of muscle atrophy. The possible signalling pathway triggering the expression of Atrogin-1 involves Src-ERK1/2-Akt- FOXO causing protein degradation. CONCLUSION: Based on the current knowledge we propose that vitamin D deficiency results from the loss of VDR function and it could be partly responsible for the development of neurodegenerative diseases in human beings. Springer Berlin Heidelberg 2019-03-04 2019 /pmc/articles/PMC6422984/ /pubmed/30830277 http://dx.doi.org/10.1007/s00421-019-04104-x Text en © The Author(s) 2019 OpenAccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Invited Review Dzik, Katarzyna Patrycja Kaczor, Jan Jacek Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
title | Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
title_full | Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
title_fullStr | Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
title_full_unstemmed | Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
title_short | Mechanisms of vitamin D on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
title_sort | mechanisms of vitamin d on skeletal muscle function: oxidative stress, energy metabolism and anabolic state |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422984/ https://www.ncbi.nlm.nih.gov/pubmed/30830277 http://dx.doi.org/10.1007/s00421-019-04104-x |
work_keys_str_mv | AT dzikkatarzynapatrycja mechanismsofvitamindonskeletalmusclefunctionoxidativestressenergymetabolismandanabolicstate AT kaczorjanjacek mechanismsofvitamindonskeletalmusclefunctionoxidativestressenergymetabolismandanabolicstate |