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Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo
BACKGROUND: The removal of permanent internal fixation devices by secondary surgery could be avoided if these devices were made of degradable magnesium and magnesium alloys. Before such implants can be used clinically, however, the biological effect of magnesium exposure on surrounding bone must be...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723563/ https://www.ncbi.nlm.nih.gov/pubmed/33313164 http://dx.doi.org/10.21037/atm-20-1921 |
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author | Chu, Wenxiang Li, Tao Jia, Gaozhi Chang, Yongyun Liu, Zhiqing Pei, Jia Yu, Degang Zhai, Zanjing |
author_facet | Chu, Wenxiang Li, Tao Jia, Gaozhi Chang, Yongyun Liu, Zhiqing Pei, Jia Yu, Degang Zhai, Zanjing |
author_sort | Chu, Wenxiang |
collection | PubMed |
description | BACKGROUND: The removal of permanent internal fixation devices by secondary surgery could be avoided if these devices were made of degradable magnesium and magnesium alloys. Before such implants can be used clinically, however, the biological effect of magnesium exposure on surrounding bone must be evaluated. Previous studies have focused on bone formation; few have examined the effects of magnesium on the bone quality that affect many biomechanical properties. METHODS: Using bone quality parameters, we analyzed in vivo changes in bone properties and biomechanics after exposure to locally high levels of magnesium. RESULTS: Local bone mineralization was significantly disrupted following exposure to a porous rod of pure magnesium. Normal crystal formation and crystallinity were inhibited and the mineral-to-matrix ratio decreased. These results were consistent with those of in vitro experiments, in which high levels of magnesium inhibited mineral deposition by mesenchymal stem cells (MSCs) but increased alkaline phosphatase (ALP) expression. The same mineralization inhibition was observed around magnesium implants via micro-computerized tomography (micro-CT) and von Kossa staining. Such reduced bone quality around degrading magnesium rods could negatively impact bone biomechanics. CONCLUSIONS: This study showed that exposure to the local high magnesium levels that arise from rapidly degrading magnesium devices may significantly disrupt bone mineralization and negatively impact bone biomechanics. |
format | Online Article Text |
id | pubmed-7723563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-77235632020-12-10 Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo Chu, Wenxiang Li, Tao Jia, Gaozhi Chang, Yongyun Liu, Zhiqing Pei, Jia Yu, Degang Zhai, Zanjing Ann Transl Med Original Article BACKGROUND: The removal of permanent internal fixation devices by secondary surgery could be avoided if these devices were made of degradable magnesium and magnesium alloys. Before such implants can be used clinically, however, the biological effect of magnesium exposure on surrounding bone must be evaluated. Previous studies have focused on bone formation; few have examined the effects of magnesium on the bone quality that affect many biomechanical properties. METHODS: Using bone quality parameters, we analyzed in vivo changes in bone properties and biomechanics after exposure to locally high levels of magnesium. RESULTS: Local bone mineralization was significantly disrupted following exposure to a porous rod of pure magnesium. Normal crystal formation and crystallinity were inhibited and the mineral-to-matrix ratio decreased. These results were consistent with those of in vitro experiments, in which high levels of magnesium inhibited mineral deposition by mesenchymal stem cells (MSCs) but increased alkaline phosphatase (ALP) expression. The same mineralization inhibition was observed around magnesium implants via micro-computerized tomography (micro-CT) and von Kossa staining. Such reduced bone quality around degrading magnesium rods could negatively impact bone biomechanics. CONCLUSIONS: This study showed that exposure to the local high magnesium levels that arise from rapidly degrading magnesium devices may significantly disrupt bone mineralization and negatively impact bone biomechanics. AME Publishing Company 2020-11 /pmc/articles/PMC7723563/ /pubmed/33313164 http://dx.doi.org/10.21037/atm-20-1921 Text en 2020 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Chu, Wenxiang Li, Tao Jia, Gaozhi Chang, Yongyun Liu, Zhiqing Pei, Jia Yu, Degang Zhai, Zanjing Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
title | Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
title_full | Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
title_fullStr | Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
title_full_unstemmed | Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
title_short | Exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
title_sort | exposure to high levels of magnesium disrupts bone mineralization in vitro and in vivo |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723563/ https://www.ncbi.nlm.nih.gov/pubmed/33313164 http://dx.doi.org/10.21037/atm-20-1921 |
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