Exercise and Testosterone Countermeasures to Mitigate Metabolic Changes during Bed Rest
: Exercise is a front-line countermeasure used to maintain astronaut health during long-duration spaceflight; however, reductions in metabolic health still occur. Accordingly, we evaluated serial changes in metabolic parameters in a spaceflight analog and evaluated the efficacy of exercise with or w...
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Published in | Life sciences in space research Vol. 26; pp. 97 - 104 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier Ltd
01.08.2020
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Subjects | |
Online Access | Get full text |
ISSN | 2214-5524 2214-5532 |
DOI | 10.1016/j.lssr.2020.03.008 |
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Abstract | : Exercise is a front-line countermeasure used to maintain astronaut health during long-duration spaceflight; however, reductions in metabolic health still occur. Accordingly, we evaluated serial changes in metabolic parameters in a spaceflight analog and evaluated the efficacy of exercise with or without the addition of low-dose testosterone treatment on mitigating adverse metabolic changes.
: Healthy young (<55 years) men were randomly assigned to one of three groups during 70-days of strict, diet controlled, 6° head-down bed rest: Control (CON, n=9), exercise plus testosterone countermeasure (TEX, n=8), or exercise countermeasure plus placebo (PEX, n=9). Basal metabolic rate (BMR), glucose tolerance, and insulin sensitivity were measured before, during, and after bed rest. Exercise energy expenditure and excess post-exercise oxygen consumption were measured in TEX and PEX subjects during bed rest.
: Leptin decreased during bed rest (Pre to BR+0 changed from 6.9 ± 5.1, 5.8 ± 4.2, and 4.7 ± 4.1 to 7.9 ±3.6, 6.5 ± 4.6, and 4.1 ±3.0 ug• L−1 for CON, PEX, and TEX respectively). Bed rest induced a decrease in BMR (Pre to BR57 changed from 1655 ± 212, 1629 ± 108, and 1706 ± 146 to 1476 ± 166, 1668 ± 142, and 1603 ± 132 kcal • day−1 ± 95%CI for CON, PEX, and TEX respectively). Similarly, bed rest negatively affected glucose metabolism assessed by 2hr OGTT glucose (Pre to BR66 changed from 6.29 ± 0.72, 5.13 ± 0.72, and 5.87 ± 0.73 to 6.62 ± 0.72, 5.83 ± 0.72, and 7.08 ± 0.72 mmol • L−1 ± 95%CI). Reambulation following bed rest positively affected glucose tolerance in CON (2hr OGTT glucose at BR+12: 5.3 ± 0.72, 6.42 ± 0.73, and 6.04 ± 0.73 mmol • L−1 ± 95%CI). Testosterone protected against bed rest induced insulin resistance (HOMA-IR from Pre to BR+66 changed from 1.74 ± 0.54, 1.18 ± 0.55, and 1.45 ± 0.56 to 2.24 ± 0.56, 1.47 ± 0.54, and 1.07 ± 0.54).
: This study confirmed that inactivity during 70 days of head-down bed rest adversely affects metabolic health. The daily exercise countermeasures were beneficial but not completely protective of bed rest induced decrements in metabolic health. Supplementary countermeasures such as testosterone may provide additional benefits not provided by exercise alone. |
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AbstractList | Exercise is a front-line countermeasure used to maintain astronaut health during long-duration spaceflight; however, reductions in metabolic health still occur. Accordingly, we evaluated serial changes in metabolic parameters in a spaceflight analog and evaluated the efficacy of exercise with or without the addition of low-dose testosterone treatment on mitigating adverse metabolic changes.
Healthy young (<55 years) men were randomly assigned to one of three groups during 70-days of strict, diet controlled, 6° head-down bed rest: Control (CON, n=9), exercise plus testosterone countermeasure (TEX, n=8), or exercise countermeasure plus placebo (PEX, n=9). Basal metabolic rate (BMR), glucose tolerance, and insulin sensitivity were measured before, during, and after bed rest. Exercise energy expenditure and excess post-exercise oxygen consumption were measured in TEX and PEX subjects during bed rest.
Leptin decreased during bed rest (Pre to BR+0 changed from 6.9 ± 5.1, 5.8 ± 4.2, and 4.7 ± 4.1 to 7.9 ±3.6, 6.5 ± 4.6, and 4.1 ±3.0 ug• L
for CON, PEX, and TEX respectively). Bed rest induced a decrease in BMR (Pre to BR57 changed from 1655 ± 212, 1629 ± 108, and 1706 ± 146 to 1476 ± 166, 1668 ± 142, and 1603 ± 132 kcal • day
± 95%CI for CON, PEX, and TEX respectively). Similarly, bed rest negatively affected glucose metabolism assessed by 2hr OGTT glucose (Pre to BR66 changed from 6.29 ± 0.72, 5.13 ± 0.72, and 5.87 ± 0.73 to 6.62 ± 0.72, 5.83 ± 0.72, and 7.08 ± 0.72 mmol • L
± 95%CI). Reambulation following bed rest positively affected glucose tolerance in CON (2hr OGTT glucose at BR+12: 5.3 ± 0.72, 6.42 ± 0.73, and 6.04 ± 0.73 mmol • L
± 95%CI). Testosterone protected against bed rest induced insulin resistance (HOMA-IR from Pre to BR+66 changed from 1.74 ± 0.54, 1.18 ± 0.55, and 1.45 ± 0.56 to 2.24 ± 0.56, 1.47 ± 0.54, and 1.07 ± 0.54).
This study confirmed that inactivity during 70 days of head-down bed rest adversely affects metabolic health. The daily exercise countermeasures were beneficial but not completely protective of bed rest induced decrements in metabolic health. Supplementary countermeasures such as testosterone may provide additional benefits not provided by exercise alone. : Exercise is a front-line countermeasure used to maintain astronaut health during long-duration spaceflight; however, reductions in metabolic health still occur. Accordingly, we evaluated serial changes in metabolic parameters in a spaceflight analog and evaluated the efficacy of exercise with or without the addition of low-dose testosterone treatment on mitigating adverse metabolic changes. : Healthy young (<55 years) men were randomly assigned to one of three groups during 70-days of strict, diet controlled, 6° head-down bed rest: Control (CON, n=9), exercise plus testosterone countermeasure (TEX, n=8), or exercise countermeasure plus placebo (PEX, n=9). Basal metabolic rate (BMR), glucose tolerance, and insulin sensitivity were measured before, during, and after bed rest. Exercise energy expenditure and excess post-exercise oxygen consumption were measured in TEX and PEX subjects during bed rest. : Leptin decreased during bed rest (Pre to BR+0 changed from 6.9 ± 5.1, 5.8 ± 4.2, and 4.7 ± 4.1 to 7.9 ±3.6, 6.5 ± 4.6, and 4.1 ±3.0 ug• L−1 for CON, PEX, and TEX respectively). Bed rest induced a decrease in BMR (Pre to BR57 changed from 1655 ± 212, 1629 ± 108, and 1706 ± 146 to 1476 ± 166, 1668 ± 142, and 1603 ± 132 kcal • day−1 ± 95%CI for CON, PEX, and TEX respectively). Similarly, bed rest negatively affected glucose metabolism assessed by 2hr OGTT glucose (Pre to BR66 changed from 6.29 ± 0.72, 5.13 ± 0.72, and 5.87 ± 0.73 to 6.62 ± 0.72, 5.83 ± 0.72, and 7.08 ± 0.72 mmol • L−1 ± 95%CI). Reambulation following bed rest positively affected glucose tolerance in CON (2hr OGTT glucose at BR+12: 5.3 ± 0.72, 6.42 ± 0.73, and 6.04 ± 0.73 mmol • L−1 ± 95%CI). Testosterone protected against bed rest induced insulin resistance (HOMA-IR from Pre to BR+66 changed from 1.74 ± 0.54, 1.18 ± 0.55, and 1.45 ± 0.56 to 2.24 ± 0.56, 1.47 ± 0.54, and 1.07 ± 0.54). : This study confirmed that inactivity during 70 days of head-down bed rest adversely affects metabolic health. The daily exercise countermeasures were beneficial but not completely protective of bed rest induced decrements in metabolic health. Supplementary countermeasures such as testosterone may provide additional benefits not provided by exercise alone. |
Author | Buxton, Roxanne E. Urban, Randall J. Randolph, Kathleen M. Ploutz-Snyder, Robert Sheffield-Moore, Melinda Goetchius, Elizabeth Danesi, Christopher P. Scott, Jessica M. Dillon, E. Lichar Downs, Meghan E. Ploutz-Snyder, Lori L. |
AuthorAffiliation | 3 University of Michigan, Ann Arbor, MI 1 National Aeronautics and Space Administration, Houston, TX 2 Memorial Sloan Kettering Cancer Center, New York, NY 6 Texas A&M University, College Station, TX 5 University of Texas Medical Branch, Galveston, TX 4 University of Houston, Houston, TX |
AuthorAffiliation_xml | – name: 3 University of Michigan, Ann Arbor, MI – name: 6 Texas A&M University, College Station, TX – name: 1 National Aeronautics and Space Administration, Houston, TX – name: 4 University of Houston, Houston, TX – name: 5 University of Texas Medical Branch, Galveston, TX – name: 2 Memorial Sloan Kettering Cancer Center, New York, NY |
Author_xml | – sequence: 1 givenname: Meghan E. surname: Downs fullname: Downs, Meghan E. organization: National Aeronautics and Space Administration, Houston, TX – sequence: 2 givenname: Jessica M. surname: Scott fullname: Scott, Jessica M. organization: Memorial Sloan Kettering Cancer Center, New York, NY – sequence: 3 givenname: Lori L. surname: Ploutz-Snyder fullname: Ploutz-Snyder, Lori L. organization: University of Michigan, Ann Arbor, MI – sequence: 4 givenname: Robert surname: Ploutz-Snyder fullname: Ploutz-Snyder, Robert organization: University of Michigan, Ann Arbor, MI – sequence: 5 givenname: Elizabeth surname: Goetchius fullname: Goetchius, Elizabeth organization: University of Houston, Houston, TX – sequence: 6 givenname: Roxanne E. surname: Buxton fullname: Buxton, Roxanne E. organization: University of Houston, Houston, TX – sequence: 7 givenname: Christopher P. surname: Danesi fullname: Danesi, Christopher P. organization: University of Texas Medical Branch, Galveston, TX – sequence: 8 givenname: Kathleen M. surname: Randolph fullname: Randolph, Kathleen M. organization: University of Texas Medical Branch, Galveston, TX – sequence: 9 givenname: Randall J. surname: Urban fullname: Urban, Randall J. organization: University of Texas Medical Branch, Galveston, TX – sequence: 10 givenname: Melinda surname: Sheffield-Moore fullname: Sheffield-Moore, Melinda organization: University of Texas Medical Branch, Galveston, TX – sequence: 11 givenname: E. Lichar surname: Dillon fullname: Dillon, E. Lichar email: edgar.l.dillon@nasa.gov organization: University of Texas Medical Branch, Galveston, TX |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32718692$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_cophys_2022_100628 crossref_primary_10_1038_s41526_023_00256_5 crossref_primary_10_1016_j_arr_2024_102227 crossref_primary_10_1016_j_cjca_2024_05_009 crossref_primary_10_3389_fphys_2022_928313 crossref_primary_10_1111_bcp_15877 crossref_primary_10_1152_japplphysiol_00468_2024 crossref_primary_10_1152_japplphysiol_00489_2023 crossref_primary_10_3389_fbioe_2022_868999 crossref_primary_10_1113_JP281800 |
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Keywords | Energy Balance Metabolic Rate Insulin Sensitivity Glucose Tolerance Spaceflight |
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Notes | Author Contributions Conception and design of study: LPS, RJU, MSM, ELD; Acquisition of data: EG, RB, CPD, KMR; Analysis and interpretation of data: MED, JMS, RPS, ELD; Drafting and revision of article: MED, JMS, ELD; All authors have approved the final article and report no conflicts of interest. |
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SubjectTerms | Adult Bed Rest Energy Balance Exercise - physiology Glucose Tolerance Humans Insulin Sensitivity Male Metabolic Rate Middle Aged Spaceflight Testosterone - therapeutic use Weightlessness Simulation Young Adult |
Title | Exercise and Testosterone Countermeasures to Mitigate Metabolic Changes during Bed Rest |
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