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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Published in | Scientific reports Vol. 9; no. 1; p. 6614 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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29.04.2019
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Abstract | 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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AbstractList | Abstract
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. 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. 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. |
ArticleNumber | 6614 |
Author | Itoh, Yoshifumi Ichimaru, Ryota Tominari, Tsukasa Matsumoto, Chiho Shirakawa, Masaki Watanabe, Kenta Shiba, Dai Inada, Masaki Miyaura, Chisato Taniguchi, Keita Yumoto, Akane Hirata, Michiko |
Author_xml | – sequence: 1 givenname: Tsukasa surname: Tominari fullname: Tominari, Tsukasa organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology – sequence: 2 givenname: Ryota surname: Ichimaru fullname: Ichimaru, Ryota organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology – sequence: 3 givenname: Keita surname: Taniguchi fullname: Taniguchi, Keita organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology – sequence: 4 givenname: Akane surname: Yumoto fullname: Yumoto, Akane organization: JEM Utilization Center, Human Spaceflight Technology Directorate, JAXA – sequence: 5 givenname: Masaki surname: Shirakawa fullname: Shirakawa, Masaki organization: JEM Utilization Center, Human Spaceflight Technology Directorate, JAXA – sequence: 6 givenname: Chiho surname: Matsumoto fullname: Matsumoto, Chiho organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology – sequence: 7 givenname: Kenta surname: Watanabe fullname: Watanabe, Kenta organization: Institute of Global Innovation Research, Tokyo University of Agriculture and Technology – sequence: 8 givenname: Michiko surname: Hirata fullname: Hirata, Michiko organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology – sequence: 9 givenname: Yoshifumi orcidid: 0000-0002-2128-2823 surname: Itoh fullname: Itoh, Yoshifumi organization: Institute of Global Innovation Research, Tokyo University of Agriculture and Technology, Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford – sequence: 10 givenname: Dai surname: Shiba fullname: Shiba, Dai organization: JEM Utilization Center, Human Spaceflight Technology Directorate, JAXA – sequence: 11 givenname: Chisato surname: Miyaura fullname: Miyaura, Chisato organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, Institute of Global Innovation Research, Tokyo University of Agriculture and Technology – sequence: 12 givenname: Masaki surname: Inada fullname: Inada, Masaki email: m-inada@cc.tuat.ac.jp organization: Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, Institute of Global Innovation Research, Tokyo University of Agriculture and Technology |
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Cell Physiol doi: 10.1152/ajpcell.00524.2003 contributor: fullname: ND Searby – volume: 10 start-page: e0128846 year: 2015 ident: 42829_CR13 publication-title: PloS One doi: 10.1371/journal.pone.0128846 contributor: fullname: S Zhou – ident: 42829_CR27 doi: 10.1007/s12576-017-0566-4 – volume: 463 start-page: 928 year: 2015 ident: 42829_CR17 publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2015.06.037 contributor: fullname: S Zhou – volume: 18 start-page: 1695 year: 2003 ident: 42829_CR12 publication-title: J Bone Miner Res doi: 10.1359/jbmr.2003.18.9.1695 contributor: fullname: M Saito – volume: 67 start-page: 271 year: 2017 ident: 42829_CR2 publication-title: J Physiol Sci doi: 10.1007/s12576-016-0514-8 contributor: fullname: K Tanaka – volume: 80 start-page: 2 year: 2015 ident: 42829_CR20 publication-title: Bone doi: 10.1016/j.bone.2015.02.028 contributor: fullname: T Endo – volume: 7 year: 2017 ident: 42829_CR25 publication-title: Sci Rep doi: 10.1038/s41598-017-10998-4 contributor: fullname: D Shiba – volume: 113 start-page: 2171 year: 2012 ident: 42829_CR1 publication-title: Eur J Appl Physiol doi: 10.1007/s00421-012-2548-9 contributor: fullname: TP Stein – volume: 23 start-page: 221 year: 1998 ident: 42829_CR11 publication-title: Cell Struct Funct doi: 10.1247/csf.23.221 contributor: fullname: K Kawashima – volume: 7 start-page: P127 year: 2000 ident: 42829_CR18 publication-title: J Gravit Physiol contributor: fullname: A Nemoto – volume: 3 start-page: 1009 year: 2001 ident: 42829_CR22 publication-title: Nat Cell Biol doi: 10.1038/ncb1101-1009 contributor: fullname: C Rommel – volume: 113 start-page: 258 year: 2012 ident: 42829_CR7 publication-title: J Biosci Bioeng doi: 10.1016/j.jbiosc.2011.09.025 contributor: fullname: G Ciofani – volume: 65 start-page: 175 year: 2016 ident: 42829_CR24 publication-title: Exp Anim doi: 10.1538/expanim.15-0077 contributor: fullname: M Shimbo – volume: 1030 start-page: 158 year: 2004 ident: 42829_CR14 publication-title: Sciences contributor: fullname: S Morita – volume: 4 start-page: 524 year: 2008 ident: 42829_CR23 publication-title: Autophagy doi: 10.4161/auto.5905 contributor: fullname: C Mammucari – volume: 10 start-page: e0133981 year: 2015 ident: 42829_CR8 publication-title: PLoS One doi: 10.1371/journal.pone.0133981 contributor: fullname: H Morita – ident: 42829_CR5 doi: 10.1002/mus.26061 – volume: 7 start-page: 30147 year: 2016 ident: 42829_CR26 publication-title: Oncotarget doi: 10.18632/oncotarget.9253 contributor: fullname: G Yoon |
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Snippet | Spaceflight is known to induce severe systemic bone loss and muscle atrophy of astronauts due to the circumstances of microgravity. We examined the influence... Abstract Spaceflight is known to induce severe systemic bone loss and muscle atrophy of astronauts due to the circumstances of microgravity. We examined the... |
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SubjectTerms | 38 38/77 631/337 64 64/60 692/699 Absorptiometry, Photon Animals Atrophy Autophagy Body Weight - physiology Bone growth Bone loss Bone mass Bone morphogenetic protein 2 Bone Morphogenetic Protein 2 - metabolism Cancellous Bone - metabolism Cancellous Bone - physiology Centrifugation Computed tomography Eating - physiology Femur Femur - metabolism Femur - physiology Gene expression Gravity Humanities and Social Sciences Humerus Humerus - metabolism Humerus - physiology Hypergravity Male Metabolism Mice Mice, Inbred C57BL Microgravity multidisciplinary Muscle, Skeletal - metabolism Muscle, Skeletal - physiology MyoD protein MyoD Protein - metabolism Myogenesis Osteogenesis Polymerase Chain Reaction Proteins Rheumatology RNA, Messenger - metabolism Science Science (multidisciplinary) Sp7 Transcription Factor - metabolism Space flight Space stations Tibia Tibia - metabolism Tibia - physiology Triceps surae muscle X-Ray Microtomography |
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Title | Hypergravity and microgravity exhibited reversal effects on the bone and muscle mass in mice |
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