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Clinical Trials/NCT02581306
NCT02581306CompletedNot Applicable

Exercise-mediated Changes in Adipocyte Differentiation and Metabolic Function

University of Michigan1 site in 1 country29 target enrollmentStarted: October 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
29
Locations
1
Primary Endpoint
changes in plasma concentrations of IL-6 after a session of exercise

Study Overview

Brief Summary

If eligible to participate in the research study after completing the physical screening procedures, participants will be asked to return to the Substrate Metabolism Laboratory on another occasion after a short fast (no food or beverages - besides water) for at least 6 hours. After participants arrive, participants will rest quietly for approximately 30 min. The investigators will then collect a blood sample from a vein in participants hand, or forearm. After obtaining a baseline blood sample, participants will exercise at a moderate intensity (on a treadmill or a stationary bike) for one hour. This one hour moderate exercise session will feel like a slow jog during which participants would be able to carry a conversation. In order for the investigators to measure energy expended and the amount of fat participants are burning during exercise, the investigators will periodically ask participants to breathe through a mouthpiece so the investigators can collect participants expired breath. After the exercise session the investigators will collect another blood sample from a vein in participants hand, or forearm.

Detailed Description

General study design

  • Subjects who exercise regularly will be instructed to exercise exactly 3 days before the experimental trial, and then abstain from their exercise training program until after the experiment is complete.

  • Subjects will arrive to the Substrate Metabolism Laboratory (1210 CCRB) after at least a 6h fast.

  • After resting quietly in the laboratory for approximately 30min, Dr. Horowitz will collect a resting blood sample by venipuncture, as he has done in our other IRB approved protocols (e.g., HUM00029179). Briefly, Dr. Horowitz will wash his hands and put on gloves. The participant's skin will be disinfected at the venipuncture site with isopropyl alcohol. Single-use needles will be used for each participant and immediately discarded into a biohazard sharps container after use. After the blood draw, direct pressure will be applied to the site of needle insertion to avoid/reduce bruising and discomfort.

  • Subjects will exercise (bike or treadmill) for 1h at a moderate exercise intensity (approximately 65% of their predicted VO2peak). This moderate exercise intensity has been used extensively by Dr. Horowitz's laboratory in previous exercise testing and training studies in both lean and obese individuals, and is well tolerated by both populations.

  • During the exercise session, subjects will wear a heart rate monitor to ensure participants are exercising at the correct exercise intensity.

  • Subjects will also use the mouthpiece and nose clip (described above) for ~5min at the beginning, middle, and end of exercise to verify they are exercising at approximately 65% of their predicted VO2peak.

  • A study team member will be present with the participant at all times during exercise to ensure the comfort and safety.

  • Immediately after exercise another blood sample will be collected.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Age: 18-40
  • •Body Mass Index: 20-35 kg/m2
  • •Women must have regularly occurring menses and must be premenopausal

Exclusion Criteria

  • •Pregnant or lactating
  • •Evidence/history of cardiovascular or metabolic disease
  • •Medications known to affect lipid or glucose metabolism

Arms & Interventions

Exercise session

Other

All subjects will exercise for 1 hour at a moderate intensity. There are no different arms in this study

Intervention: Exercise session (Other)

Outcomes

Primary Outcomes

changes in plasma concentrations of IL-6 after a session of exercise

Time Frame: 1 day

Plasma levels will be measured using appropriate commercially available assays.

changes in plasma concentrations of epinephrine after a session of exercise

Time Frame: 1 day

Plasma levels will be measured using appropriate commercially available assays.

changes in plasma concentrations of growth hormone after a session of exercise

Time Frame: 1 day

Plasma levels will be measured using appropriate commercially available assays.

changes in plasma concentrations of fatty acids after a session of exercise

Time Frame: 1 day

Plasma levels will be measured using appropriate commercially available assays.

changes in plasma concentrations of lactate after a session of exercise

Time Frame: 1 day

Plasma levels will be measured using appropriate commercially available assays.

changes in plasma concentrations of irisin after a session of exercise

Time Frame: 1 day

Plasma levels will be measured using appropriate commercially available assays.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jeffrey F Horowitz

Professor, Movement Science and Director, Substrate Metabolism Laboratory

University of Michigan

Study Sites (1)

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