Glutathione and Fuel Oxidation in Aging

Sponsor
Rajagopal V Sekhar (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT01870193
Collaborator
National Institute on Aging (NIA) (NIH)
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Study Details

Study Description

Brief Summary

Glutathione is an important antioxidant protein which protects cells from harmful oxidative stress. Elderly humans are known to have elevated oxidative stress and deficiency of glutathione, but it is not known whether there is deficient synthesis of glutathione in muscle tissue of elderly humans.

Mitochondria are engines of cells where food consumed is burned to make energy. Under normal conditions the fuel of choice in the fasted state is fat, but fasted elderly humans are not able to oxidize fat as well as healthy young humans. Elderly humans also have the highest incidence and prevalence of being overweight and obese, and have increased storage of fat in liver and muscle.

This study will help determine whether

  1. elderly humans have diminished synthesis of glutathione in the skeletal muscle, and whether this can be improved by supplementing cysteine and glycine (and not an isonitrogenous placebo) in the diet;

  2. improving muscle glutathione concentrations can also improve fuel oxidation in aging;

  3. improvement of intracellular glutathione concentrations will be associated with a change in total body fat content

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Glycine, cysteine (as n-acetylcysteine), alanine
Early Phase 1

Detailed Description

Subjects will be recruited by written informed consent on forms approved by the Institutional Review Board of Baylor College of Medicine at the time of approval of the full protocol. Subjects taking an nonvitamin supplements or lipid lowering medications will stop this 4 weeks before the screening labs and for the entire duration of the study. Fasted subjects will have screening labs (blood count, HbA1c, lipid profile, liver profile, blood urea nitrogen, Creatinine, thyroid stimulating hormone, free t4, cortisol) followed by an oral glucose tolerance test, measures of muscle strength by dynamometry, tests of function (including a 6-min walk test) and body composition scans to measure total body fat. On another occasion, fasted subjects will be undergo stable isotope infusions and other studies in the metabolic research unit to measure concentrations of amino-acids and glutathione in red blood cells and muscle tissue, glutathione synthesis rates in muscle and red cells, plasma and whole-body mitochondrial fatty-acid oxidation, Kreb's cycle function, urine urea nitrogen, plasma reactive oxygen species and F2-isoprostanes, genes of glutathione synthesis and fuel oxidation. Elderly subjects will also have magnetic resonance spectroscopy scan for liver and muscle fat content.

Young subjects will be given dietary cysteine and glycine for 2-weeks and be restudied 2-weeks later. They are then released from the study.

Elderly subjects will be studied for 16 weeks. They will be assigned to receive either cysteine plus glycine, or alanine in a randomized, double-blinded study design. The studies described above will be repeated after 2 weeks and 16 weeks. Subjects will have monthly measures of liver profile, lipid profiles, BUN and creatinine and glutathione.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Glutathione and Fuel Oxidation in Aging
Actual Study Start Date :
Apr 23, 2013
Actual Primary Completion Date :
Mar 1, 2019
Anticipated Study Completion Date :
Jun 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Young controls

Young controls will be studied before and after receiving cysteine and glycine for 2 weeks

Dietary Supplement: Glycine, cysteine (as n-acetylcysteine), alanine
Young controls will receive cysteine plus glycine for 2 weeks The elderly subjects will be randomized in a double-blinded design to receive either cysteine plus glycine OR alanine for a period of 4 months

Active Comparator: Elderly active

Elderly subjects in the active group will receive glycine plus cysteine (as n-acetylcysteine) for 4 months, and be studied at baseline, 2 weeks and 4 months

Dietary Supplement: Glycine, cysteine (as n-acetylcysteine), alanine
Young controls will receive cysteine plus glycine for 2 weeks The elderly subjects will be randomized in a double-blinded design to receive either cysteine plus glycine OR alanine for a period of 4 months

Placebo Comparator: Elderly placebo

Elderly subjects in the placebo group will receive alanine for 4 months, and be studied at baseline, 2 weeks and 4 months

Dietary Supplement: Glycine, cysteine (as n-acetylcysteine), alanine
Young controls will receive cysteine plus glycine for 2 weeks The elderly subjects will be randomized in a double-blinded design to receive either cysteine plus glycine OR alanine for a period of 4 months

Outcome Measures

Primary Outcome Measures

  1. Muscle glutathione concentration [Each subject will be studied over 4 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Elderly subjects: age range 61-80y.

  2. Young healthy subjects: age range 21-40y

Exclusion Criteria:
  1. Renal impairment (serum creatinine >1.5 mg/dL)

  2. Liver impairment (liver transaminases >2x upper limit of normal)

  3. Untreated/uncontrolled hyperthyroidism or hypothyroidism

  4. Known hypercortisolemia

  5. Known diabetes mellitus

  6. Hospitalization in the past 3 months

  7. BMI <27 (elderly group)

  8. Elderly women on estrogen replacement

  9. Known pre-existing coronary artery disease

  10. Fasted plasma triglyceride >300 mg/dl (on lipid lowering medications)

  11. Fasted plasma triglyceride >500 mg/dl (off lipid lowering medications)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Baylor College of Medicine Houston Texas United States 77030

Sponsors and Collaborators

  • Rajagopal V Sekhar
  • National Institute on Aging (NIA)

Investigators

  • Principal Investigator: R V Sekhar, MD, Baylor College of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rajagopal V Sekhar, Associate Professor, Baylor College of Medicine
ClinicalTrials.gov Identifier:
NCT01870193
Other Study ID Numbers:
  • H-30681 GSH-Aging
  • R01AG041782
First Posted:
Jun 5, 2013
Last Update Posted:
Dec 1, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Rajagopal V Sekhar, Associate Professor, Baylor College of Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 1, 2021