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Potential Dietary Countermeasure Against Spaceflight-Induced Bone LossAs humans venture further into space and beyond low Earth orbit, space radiation is one of the main challenges for astronauts' health. Radiation-induced bone loss is a potential health problem for long duration habitation in space. We showed that a dietary countermeasure prevents bone loss in mice exposed to total body irradiation (TBI). We used a range of ionizing radiation, gamma (137Cs), proton (1H), iron (56Fe), and a combination of sequential proton and iron beam (1H/56Fe/1H) to evaluate skeletal responses. These TBI cover a range of linear energy transfer (LET), from low-LET such as proton, to high-LET such as 56Fe (HZE: high Z- high energy) at doses between 1-2 Gy. The countermeasure diet, composed of 25% Dried Plum (DP) was effective at preventing radiation-induced cancellous bone loss in appendicular bone (tibia). Furthermore, exposing mice to HZE radiation, such as 56Fe (1Gy), impaired ex vivo growth of marrow-derived, bone-forming osteoblasts, which led to reduced mineralization capacity (-77%). In contrast, mice fed the DP diet did not display these deficits, showing the diet's capacity to protect marrow-derived osteoprogenitors. Dietary DP prevented the increase of bone resorbing osteoclast cells, inflammation and oxidative stress, while protecting the osteoprogenitors and mesenchymal stem cells, which few drugs against osteoporosis may achieve. Spaceflight is a combination of multiple factors including microgravity, in addition to space radiation. Therefore, we conducted additional studies to determine if the DP diet could prevent simulated spaceflight (simulated microgravity and radiation combined) bone loss. Mice were exposed to gamma (TBI, 137Cs, 2 Gy), simulated microgravity (using the hindlimb unloading system, HU) or TBI+HU. While we observed bone loss in mice fed the control diet (CD) due to both treatments (TBI=14%, HU=20%), and a worse effect with combined treatments (TBI+HU=25%), mice fed the DP diet did not sustain significant bone loss relative to untreated controls. The DP diet prevented microarchitectural decrements in both appendicular bone (tibia) and axial bone (vertebrae). In addition, the DP diet mitigated HU-induced deficits in osteoblastogenesis. Interestingly, lower doses of DP diet (5%, 10%) did not appear to prevent cancellous bone loss, which shows the importance of identifying the active component(s) of DP. Finally, we have preliminary data showing the potential of DP to prevent radiation-induced damage at a systematic level.. In summary, this novel dietary countermeasure is a promising candidate nutritional countermeasure for spaceflight-induced bone loss and tissue damage.
Document ID
20180004708
Acquisition Source
Ames Research Center
Document Type
Conference Paper
Authors
Schreurs, Ann-Sofie
(Universities Space Research Association (USRA) Moffett Field, CA, United States)
Tahimic, Candice G. T.
(Wyle Labs., Inc. Moffett Field, CA, United States)
Steczina, Sonette N.
(Blue Marble Space Seattle, WA, United States)
Terada, Masahiro
(NASA Ames Research Center Moffett Field, CA, United States)
Torres, Samantha M.
(Blue Marble Space Seattle, WA, United States)
Lowe, Moniece
(NASA Ames Research Center Moffett Field, CA, United States)
Shirazi-Fard, Yasaman
(NASA Ames Research Center Moffett Field, CA, United States)
Alwood, Joshua S.
(NASA Ames Research Center Moffett Field, CA, United States)
Globus, Ruth K.
(NASA Ames Research Center Moffett Field, CA, United States)
Date Acquired
August 28, 2018
Publication Date
July 14, 2018
Subject Category
Aerospace Medicine
Report/Patent Number
ARC-E-DAA-TN52558
Meeting Information
Meeting: COSPAR (Committee on Space Research) Scientific Assembly
Location: Pasadena, CA
Country: United States
Start Date: July 14, 2018
End Date: July 22, 2018
Sponsors: Lockheed Martin Corp.
Funding Number(s)
CONTRACT_GRANT: NNA16BD14C
CONTRACT_GRANT: NNA14AB82C
CONTRACT_GRANT: ISS-IGA-JA
CONTRACT_GRANT: NNX15AG98A
Distribution Limits
Public
Copyright
Public Use Permitted.
Keywords
Countermeasure
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