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The goal of this clinical trial is to compare the effects of resistance training (RT) preconditioning vs no training on disuse-induced atrophy and post-disuse resistance training in young healthy individuals. The main questions it aims to answer are:
Participants will:
Researchers will compare the resistance training preconditioning condition vs the non-trained condition to see if resistance training prior to a period of disuse is beneficial during the disuse period and in the return to training period on skeletal muscle size, strength, and underpinning molecular markers.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Resistance Training Preconditioning (PRECON) | Experimental | This group will perform:
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| Control (CTL) | Active Comparator | This group will perform:
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Resistance Training Preconditioning | Other | Resistance training prior to disuse-induced atrophy followed by another period of resistance training |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in vastus lateralis fiber cross-sectional area | Upon the procurement and analysis of muscle from the vastus lateralis of participants, histological techniques will be used to assess fiber cross-sectional area of muscle fibers | Through completion of study, 16 weeks |
| Change in quadriceps strength via 3 repetition maximum testing | Strength of the quadriceps will be assessed via 3-repetition maximum testing of select exercises (leg press, leg extension, hex-bar deadlift) | Through completion of study, 16 weeks |
| Change in quadriceps strength via isokinetic dynamometry | Strength of the quadriceps will be assessed via isokinetic dynamometry | Through completion of study, 16 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in protein expression of anabolic signaling proteins | Western blotting will be performed and quantified in relative fluorescence units for proteins involved in the mechanistic target of rapamycin signaling pathway. | Through completion of study, 16 weeks |
| Change in protein expression of catabolic signaling proteins |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Michael D Roberts, PhD | Contact | 334-844-1925 | mdr0024@auburn.edu | |
| John M Michel, MS | Contact | 2059077830 | michel@auburn.edu |
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| ID | Term |
|---|---|
| D020966 | Muscular Disorders, Atrophic |
| D009133 | Muscular Atrophy |
| ID | Term |
|---|---|
| D009135 | Muscular Diseases |
| D009140 | Musculoskeletal Diseases |
| D009468 | Neuromuscular Diseases |
| D009422 | Nervous System Diseases |
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| Control | Other | Activities of daily living prior to disuse-induced atrophy followed by a period of resistance training |
|
Western blotting will be performed and quantified in relative fluorescence units for proteins involved in the catabolic signaling pathways (e.g. ubiquitin-proteasome system, calpain system, autophagy). |
| Through completion of study, 16 weeks |
| Change in activity of catabolic systems | Activity assays will be performed and quantified in relative fluorescence units normalized to muscle soluble protein abundance in order to quantify the activity of the calpain system and the 20S proteasome core. | Through completion of study, 16 weeks |
| Gene expression at the mRNA level of atrophy-associated genes (atrogenes) | Real time quantitative polymerase chain reactions (qPCR) will be used to quantify the expression of select genes associated with atrophy. These data will be reported as fold-change from baseline and will be normalized to one or more housekeeping genes whose value does not change throughout the duration of the study. | Through completion of study, 16 weeks |
| D020879 | Neuromuscular Manifestations |
| D009461 | Neurologic Manifestations |
| D001284 | Atrophy |
| D020763 | Pathological Conditions, Anatomical |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D012816 | Signs and Symptoms |