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Clinical Trials/NCT02987491
NCT02987491CompletedNot Applicable

Exercise and Insulin Signaling in Human Skeletal Muscle

Oregon State University1 site in 1 country20 target enrollmentStarted: November 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
Skeletal muscle insulin sensitivity

Study Overview

Brief Summary

Obesity is associated with a decrease in skeletal muscle insulin sensitivity. Aerobic exercise can increase insulin sensitivity in the few hours following exercise, however the cellular mechanisms are not completely understood. The current project is to investigate mechanisms of exercise improvements to skeletal muscle insulin sensitivity.

Detailed Description

Study Overview: We are investigating the mechanisms by which exercise improves the response of skeletal muscle to insulin in lean and obese adults. Participants will complete 4 study visits consisting of: 1) screening visit, 2) maximal exercise test visit, and then a randomized order of 3) a resting metabolic study visit, and 4) an exercise metabolic study visit. Metabolic study visits for resting and exercise conditions will be identical, other than remaining sedentary or performing exercise. Skeletal muscle biopsy samples will be collected during resting, immediately post-exercise and during insulin stimulated conditions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Males or Females
  • •Aged 18-45 years
  • •Normal weight (body mass index [BMI] 18-26 kg/m2) or obese (BMI 30-46 kg/m2)
  • •Sedentary (< 1 hour of planned physical activity per week for ≥ 6 months)
  • •Weight stable (< 2 kg change in body mass for ≥ 6 months)
  • •Non-smokers (no tobacco or nicotine use for ≥ 1 year)

Exclusion Criteria

  • •Hypertension (systolic blood pressure >140 mmHg, diastolic blood pressure > 90mmHg)
  • •Chronic health condition including diabetes, cardiovascular disease, treated hypertension, cancer, anemia, uncontrolled hyper- or hypothyroidism.
  • •Pregnant, nursing, irregular menses or post-menopausal (if female)
  • •Hyperglycemia (fasting glucose >126 mg/dl)
  • •Hypercholesterolemia (fasting LDL>140mg/dl)
  • •Hemoglobin < 13.0 g/dl (males), < 11.5 g/dl (females)
  • •Compromised renal function (outside 135-145 mmol/L sodium, 3.5-5.1 mmol/L potassium)
  • •Lidocaine allergy
  • •Medications including β-blockers, angiotensin converting enzyme inhibitors, insulin, thiazolidinediones, metformin, sulfonylureas, chronic non-steroidal anti-inflammatory use, anti-coagulant (e.g. warfarin), current antibiotics, opiates, monoamine oxidase inhibitors, benzodiazepines, or others that may impact the study outcomes
  • •Any physical limitation that prevents a participant from safely completing the exercise test
  • •Due to the risks associated with the current protocol, individuals with a diminished capacity to consent will be excluded. Similarly, due to the need for constant, accurate participant monitoring during metabolic study activities, participants will need to clearly understand verbal and written English. Participants who cannot clearly understand verbal and written English will be excluded.

Arms & Interventions

Exercise Metabolic Study Day

Experimental

Participants will perform a single bout of moderate intensity exercise on a cycle ergometer for 60 minutes.

A total of 3 muscle biopsies will be collected throughout the study day. Insulin sensitivity will be measured using a hyperinsulinemic-euglycemic clamp with glucose tracers.

Intervention: Exercise (Behavioral)

Resting Metabolic Study Day

No Intervention

Participants will rest quietly in bed for 60 minutes and resting energy metabolism will be measured with a ventilated hood.

A total of 3 muscle biopsies will be collected throughout the study day. Insulin sensitivity will be measured using a hyperinsulinemic-euglycemic clamp with glucose tracers.

Outcomes

Primary Outcomes

Skeletal muscle insulin sensitivity

Time Frame: 2 hours following rest or exercise

Skeletal muscle insulin sensitivity will be measured by hyperinsulinemic-euglycemic clamp.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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