REX-6: IL-6 Regulation of Energy Stores During Recovery From an Acute Exercise Bout

Sponsor
Helga Ellingsgaard (Other)
Overall Status
Recruiting
CT.gov ID
NCT05349149
Collaborator
(none)
30
1
2
5
6

Study Details

Study Description

Brief Summary

The aim of the study is to investigate the role of exercise-induced IL-6 in regulating energy stores and energy metabolism during recovery after an acute exercise bout. To achieve this, 30 men will be randomized to infusion placebo or tocilizumab (IL-6 receptor antibody) combined with a 2-hour exercise bout. Stable isotope tracers will be infused to determine substrate kinetics. Indirect calorimetry will be applied to determine substrate oxidation, and muscle biopsies will be taken to determine substrate uptake and storage.

Condition or Disease Intervention/Treatment Phase
  • Drug: Tocilizumab/Actemra® (Roche)
  • Drug: Saline 9%
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized, placebo-controlled, double-blindRandomized, placebo-controlled, double-blind
Masking:
Double (Participant, Investigator)
Masking Description:
Participants and investigators will be blinded to the infusion of saline or tocilizumab
Primary Purpose:
Basic Science
Official Title:
Role of IL-6 in Regulating Energy Stores During Recovery From an Acute Exercise Bout
Anticipated Study Start Date :
Apr 1, 2022
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tocilizumab

Participants will receive one 30 min intravenous infusion of tocilizumab/Actemra® (Roche). The dose will be 8 mg/kg bodyweight or a maximum of 800mg. Tocilizumab is dissolved in 100 mL 0.9% saline.

Drug: Tocilizumab/Actemra® (Roche)
The infusion of tocilizumab will antagonize IL-6 signaling for the duration of the study, allowing us to determine the role of IL-6 in regulating energy stores following acute exercise

Placebo Comparator: Saline

As placebo, participants will receive one 30 min intravenous infusion of 100 mL 0.9% saline.

Drug: Saline 9%
The infusion of saline will serve as placebo for tocilizumab, allowing us to determine the role of IL-6 in regulating energy stores following acute exercise

Outcome Measures

Primary Outcome Measures

  1. Change in muscle glycogen content (mmol/kg/h) [Measured at 0, 120, 180 and 360 minutes]

    Comparing change in muscle glycogen in the two groups from before exercise to immediately after exercise, and after 1 hour and 4 hours of recovery

  2. Change in muscle triglycerides content [Measured at 0, 120, 180 and 360 minutes]

    Comparing change in muscle triglycerides in the two groups from before exercise to immediately after exercise, and after 1 hour and 4 hours of recovery

  3. Change in muscle expression of glucose transporter type 4 (GLUT4) [Measured at 0, 120 and 360 min]

    Comparing muscle expression of GLUT4 before and immediately after exercise and 4 hours after recovery in the two groups

  4. Change in muscle expression of fatty acid translocase (FAT/CD36) [Measured at 0, 120 and 360 min]

    Comparing muscle expression of FAT/CD36 before and immediately after exercise and 4 hours after recovery in the two groups

  5. Change in muscle expression of muscle fatty acid binding protein (FABPm) [Measured at 0, 120 and 360 min]

    Comparing muscle expression of FABPm before and immediately after exercise and 4 hours after recovery in the two groups

  6. Change in muscle expression of fatty acid transporter 4 (FATP4) [Measured at 0, 120 and 360 min]

    Comparing muscle expression of FATP4 before and immediately after exercise and 4 hours after recovery in the two groups

  7. Change in muscle expression of glycerol transporters [Measured at 0, 120 and 360 min]

    Comparing muscle expression of glycerol transporters before and immediately after exercise and 4 hours after recovery in the two groups

Secondary Outcome Measures

  1. Change in glucose rate of appearance [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing glucose rate of appearance during exercise and recovery in the two groups

  2. Change in glucose rate of disappearance [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing glucose rate of disappearance during exercise and recovery in the two groups

  3. Change in glucose concentration [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing glucose concentration during exercise and recovery in the two groups

  4. Change in glucose enrichment in intramuscular glycogen [Measured at 0, 120, 180 and 360 minutes]

    Comparing glucose enrichment in intramuscular glycogen during rest, exercise and recovery in the two groups

  5. Change in intramuscular glucose concentration [Measured at 0, 120, 180 and 360 minutes]

    Comparing intramuscular glucose concentration during rest, exercise and recovery in the two groups

  6. Change in glycogen fractional synthesis rate [Measured at 0, 120, 180 and 360 minutes]

    Comparing intramuscular glycogen fractional synthesis rate during rest, exercise and recovery in the two groups

  7. Change in gylcerol rate of appearance [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing gylcerol rate of appearance during rest, exercise and recovery in the two groups

  8. Change in gylcerol rate of disappearance [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing gylcerol rate of disappearance during rest, exercise and recovery in the two groups

  9. Change in gylcerol concentration [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing gylcerol concentration during rest, exercise and recovery in the two groups

  10. Change in palmitate rate of appearance [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing palmitate rate of appearance during rest, exercise and recovery in the two groups

  11. Change in palmitate rate of disappearance [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing palmitate rate of disappearance during rest, exercise and recovery in the two groups

  12. Change in palmitate concentration [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing palmitate kinetics during rest, exercise and recovery in the two groups

  13. Change in palmitate oxidation [Measured at -150, -60, -45, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing palmitate oxidation during rest, exercise and recovery in the two groups

  14. Change in intramuscular palmitate content [Measured at 0, 120, 180 and 360 minutes]

    Comparing intramuscular palmitate content during rest, exercise and recovery in the two groups

  15. Change in palmitate enrichment in intramuscular triglycerides [Measured at 0, 120, 180 and 360 minutes]

    Comparing palmitate enrichment in intramuscular triglycerides during rest, exercise and recovery in the two groups

  16. Change in intramuscular triglycerides fractional synthesis rate [Measured at 0, 120, 180 and 360 minutes]

    Comparing intramuscular triglycerides fractional synthesis rate during rest, exercise and recovery in the two groups

  17. Change in haemoglobin [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing haemoglobin during rest, exercise and recovery in the two groups

  18. Change in haematocrit [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing haematocrit during rest, exercise and recovery in the two groups

  19. Change in differential blood count [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing differential blood count during rest, exercise and recovery in the two groups

  20. Change in plasma IL-6 concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma IL-6 concentration during rest, exercise and recovery in the two groups

  21. Change in plasma TNF-alpha concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma TNF-alpha concentration during rest, exercise and recovery in the two groups

  22. Change in plasma IL-8 concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma IL-8 concentration during rest, exercise and recovery in the two groups

  23. Change in plasma IL-10 concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma IL-10 concentration during rest, exercise and recovery in the two groups

  24. Change in plasma IL-1beta concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma IL-1beta concentration during rest, exercise and recovery in the two groups

  25. Change in plasma IL-1Ra concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma IL-1Ra concentration during rest, exercise and recovery in the two groups

  26. Change in plasma IL-4 concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma IL-4 concentration during rest, exercise and recovery in the two groups

  27. Change in plasma sIL-6R concentration [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing plasma sIL-6R concentration during rest, exercise and recovery in the two groups

  28. Change in insulin [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing insulin during rest, exercise and recovery in the two groups

  29. Change in c-peptide [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing c-peptide during rest, exercise and recovery in the two groups

  30. Change in glucagon [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing glucagon during rest, exercise and recovery in the two groups

  31. Change in growth hormone (GH) [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing GH during rest, exercise and recovery in the two groups

  32. Change in adrenaline [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing adrenaline during rest, exercise and recovery in the two groups

  33. Change in noradrenaline [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing noradrenaline during rest, exercise and recovery in the two groups

  34. Change in cortisol [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing cortisol during rest, exercise and recovery in the two groups

  35. Change in total glucagon-like peptide-1 (GLP-1) [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing total GLP-1 during rest, exercise and recovery in the two groups

  36. Change in active GLP-1 [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing active GLP-1 during rest, exercise and recovery in the two groups

  37. Change in gastric inhibitory peptide (GIP) [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing GIP during rest, exercise and recovery in the two groups

  38. Change in peptide YY (PYY) [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing PYY during rest, exercise and recovery in the two groups

  39. Change in leptin [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing leptin during rest, exercise and recovery in the two groups

  40. Change in triglycerides [Measured at -150, -30, 10, 30, 60, 90, 120, 130, 150, 180, 210, 240, 300 and 360 minutes]

    Comparing triglycerides during rest, exercise and recovery in the two groups

Other Outcome Measures

  1. Change in muscle total antioxidant capacity (TAC) [Measured in muscle biopsies taken at 0, 120 and 360 minutes]

    Comparing muscle total antioxidant capacity (TAC) at rest, after exercise and recovery in the two groups

  2. Change in muscle superoxide levels (SOD) [Measured in muscle biopsies taken at 0, 120 and 360 minutes]

    Comparing muscle superoxide levels (SOD) at rest, after exercise and recovery in the two groups

  3. Excess post-exercise oxygen consumption [Measured at -130, 0, 60, 120, 180, 240, 300 and 360 minutes]

    Comparing excess post-exercise oxygen consumption between the two groups

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Physically active (defined as meeting the ACSM's guidelines of 2.5h per week of moderate to vigorous physical activity per week), young, healthy males will be included. Participants may be included in the study if they meet all the following criteria:

  • Age ≥ 18 years and ≤ 40 years

  • BMI < 18 and > 25 kg/m2

  • Healthy (based on screening)

  • Stable body weight for 6 months

  • ≥ 2.5h/week moderate to vigorous physical activity

Exclusion Criteria:
  • • Cardiovascular disease

  • Rheumatologic disease

  • Metabolic disease

  • Elite sports or high aerobic training status (VO2max > 60 mL O2/min/kg)

  • Frequent/chronic use of medications affecting physical performance or inflammation (NSAIDS, DMARDS, corticosteroids)

  • Aspirin use >100 mg/d

  • Thyroid disease

  • Current infection

  • Aspartate amino transferase (AST) or alanine amino transferase (ALT) >2x upper normal range

  • History of carcinoma

  • History of tuberculosis

  • Ketogenic diet

  • Smoking

  • Anemia (hematocrit <33%)

  • Neutrophil count <0,5x 109/l

  • Thrombocytes <50x 109/l or bleeding disorders

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre for Physical Activity Research, Rigshospitalet Section 7641 Copenhagen Capital Region Denmark 2100

Sponsors and Collaborators

  • Helga Ellingsgaard

Investigators

  • Study Chair: Bente K Pedersen, MD, Rigshospitalet, Denmark

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Helga Ellingsgaard, PhD, Group leader, Centre for Physical Activity Research, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT05349149
Other Study ID Numbers:
  • H-21063697
First Posted:
Apr 27, 2022
Last Update Posted:
Apr 27, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Apr 27, 2022