Recruitment

Recruitment Status
Recruiting

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
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

Participated in similar bed rest study during last 12 months
Currently taking a mitochondrial targeted antioxidant or similarly acting nutraceutical
A history of greater-than 20 pack per year smoking
...
Participated in similar bed rest study during last 12 months
Currently taking a mitochondrial targeted antioxidant or similarly acting nutraceutical
A history of greater-than 20 pack per year smoking
Glomerular filtration rate (GFR) less-than 30 mL/min/1.73m2 or evidence of kidney disease or failure
Elevated systolic pressure greater-than 150 or a diastolic blood pressure greater-than 100 (treated or untreated)
Exercise training (greater-than 1 session of moderate to high intensity aerobic or resistance exercise/week)
Respiratory disease (acute upper respiratory infection, history of chronic lung disease with resting oxygen saturation less-than 97% on room air)
Cancer or history of successfully treated cancer (less than 1 year) other than basal cell carcinoma
Uncontrolled endocrine or metabolic disease (e.g., hypo/hyperthyroidism, diabetes)
History of stroke with motor disability
HIV or hepatitis B or C*
Subjects with hemoglobin or hematocrit lower than accepted lab values
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).
Cardiac abnormalities considered exclusionary by the study physician (e.g., congestive heart failure (CHF), coronary artery disease (CAD), right-to-left shunt)
Recent anabolic or corticosteroids use (within 3 months)
Use of anticoagulant therapy (e.g., Coumadin, heparin)
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
Liver disease (aspartate aminotransferase/alanine aminotransferase 2 times above the normal limit, hyperbilirubinemia)
Agitation/aggression disorder (by psychiatric history and exam)
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)
Inability to abstain from smoking for duration of study
Any other condition or event considered exclusionary by the PI and faculty physician
Unwilling to cease dietary supplements 4 weeks prior to initiation of bed rest
Implanted electronic devices (e.g., pacemakers, electronic infusion pumps, stimulators)
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)
A recent history (less-than 12 months) of GI bleed
Depression [greater-than 5 on the 15 items Geriatric Depression Scale (GDS)]

Summary

Conditions
  • Aging
  • Antioxidants
  • Oxidative Stress
  • Skeletal Muscle
  • Vascular Endothelium
Type
Interventional
Design
  • Allocation: Randomized
  • Intervention Model: Parallel Assignment
  • Intervention Model Description: Randomized double blind parallel 3 group studyMasking: Double (Participant, Investigator)
  • Masking Description: Double blind placebo controlled designPrimary Purpose: Diagnostic

Participation Requirements

Age
Between 65 years and 85 years
Gender
Both males and females

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 dysfu...

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).

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
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

Participated in similar bed rest study during last 12 months
Currently taking a mitochondrial targeted antioxidant or similarly acting nutraceutical
A history of greater-than 20 pack per year smoking
...
Participated in similar bed rest study during last 12 months
Currently taking a mitochondrial targeted antioxidant or similarly acting nutraceutical
A history of greater-than 20 pack per year smoking
Glomerular filtration rate (GFR) less-than 30 mL/min/1.73m2 or evidence of kidney disease or failure
Elevated systolic pressure greater-than 150 or a diastolic blood pressure greater-than 100 (treated or untreated)
Exercise training (greater-than 1 session of moderate to high intensity aerobic or resistance exercise/week)
Respiratory disease (acute upper respiratory infection, history of chronic lung disease with resting oxygen saturation less-than 97% on room air)
Cancer or history of successfully treated cancer (less than 1 year) other than basal cell carcinoma
Uncontrolled endocrine or metabolic disease (e.g., hypo/hyperthyroidism, diabetes)
History of stroke with motor disability
HIV or hepatitis B or C*
Subjects with hemoglobin or hematocrit lower than accepted lab values
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).
Cardiac abnormalities considered exclusionary by the study physician (e.g., congestive heart failure (CHF), coronary artery disease (CAD), right-to-left shunt)
Recent anabolic or corticosteroids use (within 3 months)
Use of anticoagulant therapy (e.g., Coumadin, heparin)
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
Liver disease (aspartate aminotransferase/alanine aminotransferase 2 times above the normal limit, hyperbilirubinemia)
Agitation/aggression disorder (by psychiatric history and exam)
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)
Inability to abstain from smoking for duration of study
Any other condition or event considered exclusionary by the PI and faculty physician
Unwilling to cease dietary supplements 4 weeks prior to initiation of bed rest
Implanted electronic devices (e.g., pacemakers, electronic infusion pumps, stimulators)
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)
A recent history (less-than 12 months) of GI bleed
Depression [greater-than 5 on the 15 items Geriatric Depression Scale (GDS)]

Locations

Salt Lake City, Utah, 84148
Salt Lake City, Utah, 84148

Tracking Information

NCT #
NCT04351113
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
Investigators
Not Provided