Simulating the Lunar Environment: Partial Weightbearing and High-LET Radiation-Induce Bone Loss and Increase Sclerostin-Positive Osteocytes

B. R. Macias, F. Lima, J. M. Swift, Y. Shirazi-Fard, E. S. Greene, M. R. Allen, J. Fluckey, H. A. Hogan, L. Braby, Suojin Wang, S. A. Bloomfield

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Exploration missions to the Moon or Mars will expose astronauts to galactic cosmic radiation and low gravitational fields. Exposure to reduced weightbearing and radiation independently result in bone loss. However, no data exist regarding the skeletal consequences of combining low-dose, high-linear energy transfer (LET) radiation and partial weightbearing. We hypothesized that simulated galactic cosmic radiation would exacerbate bone loss in animals held at one-sixth body weight (G/6) without radiation exposure. Female BALB/cByJ four-month-old mice were randomly assigned to one of the following treatment groups: 1 gravity (1G) control; 1G with radiation; G/6 control; and G/6 with radiation. Mice were exposed to either silicon-28 or X-ray radiation. 28Si radiation (300 MeV/nucleon) was administered at acute doses of 0 (sham), 0.17 and 0.5 Gy, or in three fractionated doses of 0.17 Gy each over seven days. X radiation (250 kV) was administered at acute doses of 0 (sham), 0.17, 0.5 and 1 Gy, or in three fractionated doses of 0.33 Gy each over 14 days. Bones were harvested 21 days after the first exposure. Acute 1 Gy X-ray irradiation during G/6, and acute or fractionated 0.5 Gy 28Si irradiation during 1G resulted in significantly lower cancellous mass [percentage bone volume/total volume (%BV/TV), by microcomputed tomography]. In addition, G/6 significantly reduced %BV/TV compared to 1G controls. When acute X-ray irradiation was combined with G/6, distal femur %BV/TV was significantly lower compared to G/6 control. Fractionated X-ray irradiation during G/6 protected against radiation-induced losses in %BV/TV and trabecular number, while fractionated 28Si irradiation during 1G exacerbated the effects compared to single-dose exposure. Impaired bone formation capacity, measured by percentage mineralizing surface, can partially explain the lower cortical bone thickness. Moreover, both partial weightbearing and 28Si-ion exposure contribute to a higher proportion of sclerostin-positive osteocytes in cortical bone. Taken together, these data suggest that partial weightbearing and low-dose, high-LET radiation negatively impact maintenance of bone mass by lowering bone formation and increasing bone resorption. The impaired bone formation response is associated with sclerostin-induced suppression of Wnt signaling. Therefore, exposure to low-dose, high-LET radiation during long-duration spaceflight missions may reduce bone formation capacity, decrease cancellous bone mass and increase bone resorption. Future countermeasure strategies should aim to restore mechanical loads on bone to those experienced in one gravity. Moreover, low-doses of high-LET radiation during long-duration spaceflight should be limited or countermeasure strategies employed to mitigate bone loss.

Original languageEnglish
Pages (from-to)254-263
Number of pages10
JournalRadiation Research
Volume186
Issue number3
DOIs
StatePublished - Sep 2016

Bibliographical note

Publisher Copyright:
© 2016 by Radiation Research Society.

Funding

We would like to thank Evelyn Yuen, Kaleigh Camp, Katie Elmer and David Cunningham for their excellent technical support on these laborintensive experiments. We are grateful for the expert assistance of the BNL Medical Department staff (M. Petry, K. Bonti, L. Thompson and P. Guida) and NSRL physicists (A. Rusek and M. Sievertz), which was essential to the success of our NSRL experiments at BNL. These studies were funded through the NASA Cooperative Agreement NCC 9-58 with the National Space Biomedical Research Institute (SAB). Supported was also provided by a National Space Biomedical Research Institute Graduate Training Fellowship (no. NSBRI-RFP-05-02; JMS and BRM) and the National Science Foundation Graduate Research Fellowship Program (BRM).

FundersFunder number
National Science Foundation (NSF)
National Aeronautics and Space AdministrationNCC 9-58
National Space Biomedical Research Institute
Sächsische AufbaubankNSBRI-RFP-05-02

    ASJC Scopus subject areas

    • Biophysics
    • Radiation
    • Radiology Nuclear Medicine and imaging

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