| Literature DB >> 28649627 |
Joshua S Alwood1, April E Ronca1,2, Richard C Mains3, Mark J Shelhamer4, Jeffrey D Smith1, Thomas J Goodwin5.
Abstract
NASA's Space Biology and Human Research Program entities have recently spearheaded communications both internally and externally to coordinate the agency's translational research efforts. In this paper, we strongly advocate for translational research at NASA, provide recent examples of NASA sponsored early-stage translational research, and discuss options for a path forward. Our overall objective is to help in stimulating a collaborative research across multiple disciplines and entities that, working together, will more effectively and more rapidly achieve NASA's goals for human spaceflight.Entities:
Year: 2017 PMID: 28649627 PMCID: PMC5460236 DOI: 10.1038/s41526-016-0002-8
Source DB: PubMed Journal: NPJ Microgravity ISSN: 2373-8065 Impact factor: 4.415
Fig. 1The NASA Life Sciences Translational Path. It moves from basic research to human exploration applications with bi-directionality options. As knowledge is applied along this path (top arrows) questions may arise that can best be addressed by more basic research (bottom arrows) in order to support further progress toward successful human exploration
Fig. 2Space Biology and Human Research Bi-directional Synergism. Basic Space Biology research is done mainly with lower-level model organisms, cells, and tissues. The HRP conducts biomedical science mainly with humans. They synergistically and bi-directionally collaborate in maximizing opportunities for translating a subset of that knowledge to optimize the health and safety of the crew via applications supporting medical operations
Animal and human biology (AH) research recommendations for humans in the space environment identified in chapter 6 of the decadal survey (3)
| Identifier | Recommendation |
|---|---|
| AH1 | The efficacy of bisphosphonates should be tested in an adequate population of astronauts on the ISS during a 6-month mission. |
| AH2 | The preservation/reversibility of bone structure/strength should be evaluated when assessing countermeasures. |
| AH3 | Bone loss studies of genetically altered mice exposed to weightlessness are strongly recommended. |
| AH4 | New osteoporosis drugs under clinical development should be tested in animal models of weightlessness. |
| AH5 | Conduct studies to identify underlying mechanisms regulating net skeletal muscle protein balance and protein turnover during states of unloading and recovery. |
| AH6 | Conduct studies to develop and test new prototype exercise devices and to optimize physical activity paradigms/prescriptions targeting multisystem countermeasures. |
| AH7 | Determine the daily levels and pattern of recruitment of flexor and extensor muscles of the neck, trunk, arms, and legs at 1 g and after being in a novel gravitational environment for up to 6 months. |
| AH8 | Determine the basic mechanisms, adaptations, and clinical significance of changes in regional vascular/interstitial pressures (starling forces) during long-duration space missions. |
| AH9 | Investigate the effects of prolonged periods of microgravity and partial gravity (3/8 or 1/6 g) on the determinants of task-specific, enabling levels of work capacity. |
| AH10 | Determine the integrative mechanisms of orthostatic intolerance after restoration of gravitational gradients (both 1 and 3/8 g). |
| AH11 | Collaborative studies among flight medicine and cardiovascular epidemiologists are recommended to determine the best screening strategies to avoid flying astronauts with subclinical coronary heart disease that could become manifest during a long-duration exploration-class mission (3 years). |
| AH12 | Determine the amount and site of the deposition of aerosols of different sizes in the lungs of humans and animals in microgravity. |
| AH13 | Multiple parameters of T cell activation in cells should be obtained from astronauts before and after re-entry to establish which parameters are altered during flight. |
| AH14 | Both to address the mechanism(s) of the changes in the immune system and to develop measures to limit the changes, data from multiple organ/system-based studies need to be integrated. |
| AH15 | Perform mouse studies of immunization and challenge on the ISS, using immune samples acquired both prior to and immediately upon re-entry, to establish the biological relevance of the changes observed in the immune system. Parameters examined need to be aligned with those in humans influenced by flight. |
| AH16 | Studies should be conducted on transmission across generations of structural and functional changes induced by exposure to space during development. Ground-based studies should be conducted to develop specialized habitats to support reproducing and developing rodents in space. |
Reprinted with permission from Recapturing a Future for Space Exploration: Life and Physical Sciences Research for a New Era (2011) by the National Academy of Sciences, Courtesy of the National Academies Press, Washington D.C.
Crosscutting Issues (CC) for Humans in the Space Environment identified in Chapter 7 of the Decadal Survey (3)
| Identifier | Recommendation |
|---|---|
| CC1 | To ensure the safety of future commercial orbital and exploration crews, quantify post-landing vertigo and orthostatic intolerance in a sufficiently large sample of returning ISS crews, as part of the immediate post-flight medical exam. |
| CC2 | Determine whether AG is needed as a multisystem countermeasure and whether continuous large radius AG is needed or intermittent exercise within lower-body negative pressure or short-radius AG is sufficient. Human studies in ground laboratories are essential to establish dose-response relationships, and what gravity level, gradient, rotations per minute, duration, and frequency are adequate. |
| CC3 | Conduct studies on humans to determine whether there is an effect of gravity on micronucleation and/or intrapulmonary shunting or whether the unexpectedly low prevalence of decompression sickness on the space shuttle/ISS is due to underreporting. Conduct studies to determine operationally acceptable low suit pressure and hypobaric hypoxia limits. |
| CC4 | Determine optimal dietary strategies for crews and food preservation strategies that will maintain bioavailability for 12 or more months. |
| CC5 | Initiate a robust food science program focused on preserving nutrient stability for 3 or more years. |
| CC6 | Include food and energy intake as an outcome variable in dietary intervention trials in humans. |
| CC7 | Conduct longitudinal studies of astronauts for cataract incidence, quality, and pathology related to radiation exposures to understand both cataract risk and radiation-induced late tissue toxicities in humans. |
| CC8 | Expand the use of animal studies to assess space radiation risks to humans from cancer, cataracts, cardiovascular disease, neurologic dysfunction, degenerative diseases, and acute toxicities such as fever, nausea, bone marrow suppression, and others. |
| CC9 | Continue ground-based cellular studies to develop end points and markers for acute and late radiation toxicities, using radiation facilities that are able to mimic space radiation exposures. |
| CC10 | Expand understanding of gender differences in adaptation to the spaceflight environment through flight- and ground-based research, particularly potential differences in bone, muscle, and cardiovascular function and longterm radiation risks. |
| CC11 | Investigate the biophysical principles of thermal balance to determine whether microgravity reduces the threshold for thermal intolerance. |
Reprinted with permission from Recapturing a Future for Space Exploration: Life and Physical Sciences Research for a New Era (2011) by the National Academy of Sciences, Courtesy of the National Academies Press, Washington DC