- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04351113
Targeting Oxidative Stress to Prevent Vascular and Skeletal Muscle Dysfunction During Disuse
Study Overview
Status
Detailed Description
Disuse following injury or during acute hospitalization is associated with a host of negative outcomes including functional deficiencies, hospital readmission, disability, and increased mortality. Older adults are a particularly vulnerable population as functional (vascular and skeletal muscle dysfunction) and structural deficits (loss in muscle mass leading to a reduction in strength) are present as a consequence of the aging process. Any additional and accelerated insult caused by disuse poses a serious health threat to these older individuals by depleting their already diminished physiological and functional reserve and hastening the onset of disability. Current strategies aimed at preserving function during disuse have focused on preserving skeletal muscle mass and strength while the critical role of the vasculature has been largely ignored. Moreover, the underlying cause of dysfunction has not been adequately addressed in humans. This disintegrated and myopic approach likely contributes to the fact that interventions capable of preserving health during disuse do not exist. The vascular and skeletal muscle systems are inextricably linked to optimal mobility through oxygen and nutrient delivery, thus, vascular dysfunction likely contributes to and exacerbates skeletal muscle deficiencies that occur during disuse. To fully understand the impact of disuse on health and mobility and develop effective countermeasures it is our contention that both the vascular and musculoskeletal systems must be examined and the root cause of the problem must be addressed. While the underlying factors leading to these accelerated losses during disuse are unknown, they appear to be mechanistically linked to oxidative stress.
The long term goal is to minimize losses in vascular and skeletal muscle function that occur during disuse in order to maintain functional reserve and avoid serious adverse events. The objective here, which is the next step in pursuit of this goal, is to determine how oxidative stress contributes to disuse-induced vascular and skeletal muscle dysfunction. It is our central hypothesis that oxidative stress triggers the accelerated declines in vascular and skeletal muscle function during disuse. To test this hypothesis and provide compelling evidence that oxidative stress is the trigger of dysfunction the investigators will utilize two novel and fundamentally distinct strategies to improve redox balance during disuse. In Aim 1, the mitochondrial targeted antioxidant (MITO-AO) mitoquinone will be administered during disuse to improve free radical scavenging at the level of the mitochondria. In Aim 2, activation of Nuclear Factor Erythroid-2-like 2 (Nrf2) the "master regulator of antioxidant enzymes" will be accomplished with PB125 (a novel naturally occurring Nrf2 activator) to augment endogenous antioxidant defense systems. The impact of these interventions on measures of isolated and integrated vascular and skeletal muscle function before and after disuse will be examined. The central hypothesis is supported by preliminary data reporting substantial losses in vascular and skeletal muscle function and concomitant increases in oxidative stress following 5 days of bed rest. Importantly, MITO-AO prevents disuse-induced losses in muscle mass and restores age-related deficits in vascular function in aged animals and humans (preliminary data). Additionally, PB125 activates the Nrf2 pathway at multiple control points resulting in prolonged and amplified activation and subsequent gene expression of key antioxidant enzymes leading to a decrease in oxidative stress in humans (preliminary data).
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Joel D Trinity, PhD
- Phone Number: 801-584-2522
- Email: joel.trinity@hsc.utah.edu
Study Locations
-
-
Utah
-
Salt Lake City, Utah, United States, 84148
- Recruiting
- VA Medical Center
-
Contact:
- Joel Trinity, PhD.
- Phone Number: 512-689-2187
- Email: joel.trinity@hsc.utah.edu
-
Contact:
- J. David Symons, PhD.
- Phone Number: 801-581-4769
- Email: j.david.symons@hsc.utah.edu
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 65-85 yrs
- Ability to sign informed consent
- Montreal cognitive assessment (MOCA) exam score greater-than or equal to 26 4. Free-living, prior to admission
Exclusion Criteria:
- Cardiac abnormalities considered exclusionary by the study physician (e.g., congestive heart failure (CHF), coronary artery disease (CAD), right-to-left shunt)
- Uncontrolled endocrine or metabolic disease (e.g., hypo/hyperthyroidism, diabetes)
- Glomerular filtration rate (GFR) less-than 30 mL/min/1.73m2 or evidence of kidney disease or failure
- Vascular disease or risk factors of peripheral atherosclerosis. (e.g., uncontrolled hypertension, obesity, diabetes, hypercholesterolemia greater-than 250 mg/dl, claudication or evidence of venous or arterial insufficiency upon palpitation of femoral, popliteal and pedal arteries)
- Risk of deep vein thrombosis (DVT) including family history of thrombophilia, DVT, pulmonary emboli, myeloproliferative diseases including polycythemia (Hb greater-than 18 g/dL) or thrombocytosis (platelets greater-than 400x103/mL), and connective tissue diseases (positive lupus anticoagulant), hyperhomocysteinemia, deficiencies of factor V Leiden, proteins S and C, and antithrombin III
- Use of anticoagulant therapy (e.g., Coumadin, heparin)
- Elevated systolic pressure greater-than 150 or a diastolic blood pressure greater-than 100 (treated or untreated)
- Implanted electronic devices (e.g., pacemakers, electronic infusion pumps, stimulators)
- Cancer or history of successfully treated cancer (less than 1 year) other than basal cell carcinoma
- Currently on a weight-loss diet or body mass index greater-than 35 kg/m2 (a BMI of 35 kg/m2, which includes individuals that fall into to the Class I obesity category, has been selected to improve inclusion and generalizability to a greater percentage of the general population).
- Inability to abstain from smoking for duration of study
- A history of greater-than 20 pack per year smoking
- HIV or hepatitis B or C*
- Recent anabolic or corticosteroids use (within 3 months)
- Subjects with hemoglobin or hematocrit lower than accepted lab values
- Agitation/aggression disorder (by psychiatric history and exam)
- History of stroke with motor disability
- A recent history (less-than 12 months) of GI bleed
- Depression [greater-than 5 on the 15 items Geriatric Depression Scale (GDS)]
- Alcohol abuse (greater-than 2 drinks per day) or drug abuse (inappropriate use of prescription medications or use of any illicit/illegal drugs for recreational use)
- Exercise training (greater-than 1 session of moderate to high intensity aerobic or resistance exercise/week)
- Liver disease (aspartate aminotransferase/alanine aminotransferase 2 times above the normal limit, hyperbilirubinemia)
- Respiratory disease (acute upper respiratory infection, history of chronic lung disease with resting oxygen saturation less-than 97% on room air)
- Currently taking a mitochondrial targeted antioxidant or similarly acting nutraceutical
- Unwilling to cease dietary supplements 4 weeks prior to initiation of bed rest
- Participated in similar bed rest study during last 12 months
- Any other condition or event considered exclusionary by the PI and faculty physician
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: MITO-AO
Healthy older adult subjects ages 65-75 will take the supplement MITO-AO during a 5 day bed rest and will be assessed for vascular function independent of metabolism with passive leg movement (PLM), skeletal muscle bioenergetics independent of vascular constraints (i.e.
blood flow and O2 supply) with phosphorous magnetic resonance spectroscopy (31P-MRS), and skeletal muscle bioenergetics under normal blood flow and O2 supply.
|
Participants will receive 160 mg with breakfast on day 1 of bed rest and 40 mg with breakfast on days 2-5.
Participants will be tested for passive leg movement on baseline day 1, bed rest day 1, and post bed rest.
Participants will undergo plantar flexion on baseline day 2, pre bed rest, and post bed rest.
Participants will undergo isometric knee extension on baseline day 2, pre bed rest, and post bed rest.
Participants will undergo 5 days bed rest after 5 day baseline assessments
|
Experimental: PB-125
Healthy older adult subjects ages 65-75 will take the supplement PB-125 during a 5 day bed rest and will be assessed for vascular function independent of metabolism with passive leg movement (PLM), skeletal muscle bioenergetics independent of vascular constraints (i.e.
blood flow and O2 supply) with phosphorous magnetic resonance spectroscopy (P-MRS), and skeletal muscle bioenergetics under normal blood flow and O2 supply.
|
Participants will be tested for passive leg movement on baseline day 1, bed rest day 1, and post bed rest.
Participants will undergo plantar flexion on baseline day 2, pre bed rest, and post bed rest.
Participants will undergo isometric knee extension on baseline day 2, pre bed rest, and post bed rest.
Participants will undergo 5 days bed rest after 5 day baseline assessments
Participants will receive 100 mg on days 1-5 of bed rest.
|
Placebo Comparator: Placebo
Healthy older adult subjects ages 65-75 will take placebo during a 5 day bed rest and will be assessed for vascular function independent of metabolism with passive leg movement (PLM), skeletal muscle bioenergetics independent of vascular constraints (i.e.
blood flow and O2 supply) with phosphorous magnetic resonance spectroscopy (P-MRS), and skeletal muscle bioenergetics under normal blood flow and O2 supply.
|
Participants will be tested for passive leg movement on baseline day 1, bed rest day 1, and post bed rest.
Participants will undergo plantar flexion on baseline day 2, pre bed rest, and post bed rest.
Participants will undergo isometric knee extension on baseline day 2, pre bed rest, and post bed rest.
Participants will undergo 5 days bed rest after 5 day baseline assessments
Participants will receive Placebo on days 1-5 of bed rest.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in blood vessel diameter after PLM
Time Frame: 10 days
|
10 days
|
Change in blood vessel flow rate after PLM
Time Frame: 10 days
|
10 days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in O2 augmented maximal mitochondrial oxidative capacity (Vmax) after plantar flexion
Time Frame: 10 days
|
10 days
|
Change in phosphocreatinine concentration [PCr] after plantar flexion
Time Frame: 10 days
|
10 days
|
Change in inorganic phosphate concentration [Pi] after plantar flexion
Time Frame: 10 days
|
10 days
|
Change in adenosine triphosphate (ATP) concentration after plantar flexion
Time Frame: 10 days
|
10 days
|
Change in muscle mass as measured in kilograms by dual-energy X-ray absorptiometry (DXA) after bed rest.
Time Frame: 10 days
|
10 days
|
Change in muscle strength as measured in kilograms after isometric knee extensor testing
Time Frame: 10 days
|
10 days
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB_00111321
- 1R01HL142603-01A1 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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