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The role of circadian rhythm in osteoporosis; a review

Osteoporosis is characterized by a high incidence rate, with significant effects on people’s lives. The underlying mechanisms are complex, with no treatments for the condition. Recent studies have indicated that melatonin can be used to treat osteoporosis by promoting osteoblast proliferation and di...

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Autores principales: Tian, Yihao, Ming, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550872/
https://www.ncbi.nlm.nih.gov/pubmed/36238690
http://dx.doi.org/10.3389/fcell.2022.960456
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author Tian, Yihao
Ming, Jian
author_facet Tian, Yihao
Ming, Jian
author_sort Tian, Yihao
collection PubMed
description Osteoporosis is characterized by a high incidence rate, with significant effects on people’s lives. The underlying mechanisms are complex, with no treatments for the condition. Recent studies have indicated that melatonin can be used to treat osteoporosis by promoting osteoblast proliferation and differentiation, and inhibiting osteoclast differentiation. Specifically, in vivo mechanisms are initiated by stabilizing biological rhythms in bone tissue. In healthy organisms, these biological rhythms are present in bone tissue, and are characterized by bone formation during the day, and bone resorption at night. When this rhythm is disrupted, osteoporosis occurs. Thus, taking appropriate medication at different times of the day could produce different effects on osteoporosis rhythms. In this review, we characterized these processes, and provided treatments and management strategies for individuals with osteoporosis.
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spelling pubmed-95508722022-10-12 The role of circadian rhythm in osteoporosis; a review Tian, Yihao Ming, Jian Front Cell Dev Biol Cell and Developmental Biology Osteoporosis is characterized by a high incidence rate, with significant effects on people’s lives. The underlying mechanisms are complex, with no treatments for the condition. Recent studies have indicated that melatonin can be used to treat osteoporosis by promoting osteoblast proliferation and differentiation, and inhibiting osteoclast differentiation. Specifically, in vivo mechanisms are initiated by stabilizing biological rhythms in bone tissue. In healthy organisms, these biological rhythms are present in bone tissue, and are characterized by bone formation during the day, and bone resorption at night. When this rhythm is disrupted, osteoporosis occurs. Thus, taking appropriate medication at different times of the day could produce different effects on osteoporosis rhythms. In this review, we characterized these processes, and provided treatments and management strategies for individuals with osteoporosis. Frontiers Media S.A. 2022-09-27 /pmc/articles/PMC9550872/ /pubmed/36238690 http://dx.doi.org/10.3389/fcell.2022.960456 Text en Copyright © 2022 Tian and Ming. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Tian, Yihao
Ming, Jian
The role of circadian rhythm in osteoporosis; a review
title The role of circadian rhythm in osteoporosis; a review
title_full The role of circadian rhythm in osteoporosis; a review
title_fullStr The role of circadian rhythm in osteoporosis; a review
title_full_unstemmed The role of circadian rhythm in osteoporosis; a review
title_short The role of circadian rhythm in osteoporosis; a review
title_sort role of circadian rhythm in osteoporosis; a review
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550872/
https://www.ncbi.nlm.nih.gov/pubmed/36238690
http://dx.doi.org/10.3389/fcell.2022.960456
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