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Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice

Spaceflight is known to induce severe systemic bone loss and muscle atrophy of astronauts due to the circumstances of microgravity. We examined the influence of artificially produced 2G hypergravity on mice for bone and muscle mass with newly developed centrifuge device. We also analyzed the effects...

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Autores principales: Tominari, Tsukasa, Ichimaru, Ryota, Taniguchi, Keita, Yumoto, Akane, Shirakawa, Masaki, Matsumoto, Chiho, Watanabe, Kenta, Hirata, Michiko, Itoh, Yoshifumi, Shiba, Dai, Miyaura, Chisato, Inada, Masaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488638/
https://www.ncbi.nlm.nih.gov/pubmed/31036903
http://dx.doi.org/10.1038/s41598-019-42829-z
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author Tominari, Tsukasa
Ichimaru, Ryota
Taniguchi, Keita
Yumoto, Akane
Shirakawa, Masaki
Matsumoto, Chiho
Watanabe, Kenta
Hirata, Michiko
Itoh, Yoshifumi
Shiba, Dai
Miyaura, Chisato
Inada, Masaki
author_facet Tominari, Tsukasa
Ichimaru, Ryota
Taniguchi, Keita
Yumoto, Akane
Shirakawa, Masaki
Matsumoto, Chiho
Watanabe, Kenta
Hirata, Michiko
Itoh, Yoshifumi
Shiba, Dai
Miyaura, Chisato
Inada, Masaki
author_sort Tominari, Tsukasa
collection PubMed
description Spaceflight is known to induce severe systemic bone loss and muscle atrophy of astronauts due to the circumstances of microgravity. We examined the influence of artificially produced 2G hypergravity on mice for bone and muscle mass with newly developed centrifuge device. We also analyzed the effects of microgravity (mostly 0G) and artificial produced 1G in ISS (international space station) on mouse bone mass. Experiment on the ground, the bone mass of humerus, femur and tibia was measured using micro-computed tomography (μCT), and the all bone mass was significantly increased in 2G compared with 1G control. In tibial bone, the mRNA expression of bone formation related genes such as Osx and Bmp2 was elevated. The volume of triceps surae muscle was also increased in 2G compared with 1G control, and the mRNA expression of myogenic factors such as Myod and Myh1 was elevated by 2G. On the other hand, microgravity in ISS significantly induced the loss of bone mass on humerus and tibia, compared with artificial 1G induced by centrifugation. Here, we firstly report that bone and muscle mass are regulated by the gravity with loaded force in both of positive and negative on the ground and in the space.
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spelling pubmed-64886382019-05-16 Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice Tominari, Tsukasa Ichimaru, Ryota Taniguchi, Keita Yumoto, Akane Shirakawa, Masaki Matsumoto, Chiho Watanabe, Kenta Hirata, Michiko Itoh, Yoshifumi Shiba, Dai Miyaura, Chisato Inada, Masaki Sci Rep Article Spaceflight is known to induce severe systemic bone loss and muscle atrophy of astronauts due to the circumstances of microgravity. We examined the influence of artificially produced 2G hypergravity on mice for bone and muscle mass with newly developed centrifuge device. We also analyzed the effects of microgravity (mostly 0G) and artificial produced 1G in ISS (international space station) on mouse bone mass. Experiment on the ground, the bone mass of humerus, femur and tibia was measured using micro-computed tomography (μCT), and the all bone mass was significantly increased in 2G compared with 1G control. In tibial bone, the mRNA expression of bone formation related genes such as Osx and Bmp2 was elevated. The volume of triceps surae muscle was also increased in 2G compared with 1G control, and the mRNA expression of myogenic factors such as Myod and Myh1 was elevated by 2G. On the other hand, microgravity in ISS significantly induced the loss of bone mass on humerus and tibia, compared with artificial 1G induced by centrifugation. Here, we firstly report that bone and muscle mass are regulated by the gravity with loaded force in both of positive and negative on the ground and in the space. Nature Publishing Group UK 2019-04-29 /pmc/articles/PMC6488638/ /pubmed/31036903 http://dx.doi.org/10.1038/s41598-019-42829-z Text en © The Author(s) 2019 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
Tominari, Tsukasa
Ichimaru, Ryota
Taniguchi, Keita
Yumoto, Akane
Shirakawa, Masaki
Matsumoto, Chiho
Watanabe, Kenta
Hirata, Michiko
Itoh, Yoshifumi
Shiba, Dai
Miyaura, Chisato
Inada, Masaki
Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
title Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
title_full Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
title_fullStr Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
title_full_unstemmed Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
title_short Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
title_sort hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488638/
https://www.ncbi.nlm.nih.gov/pubmed/31036903
http://dx.doi.org/10.1038/s41598-019-42829-z
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