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Impact of Acute Exercise Intensity and Pattern on Cytokine Function

Impact of Acute Exercise Intensity and Pattern on Cytokine Function

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05574413
Acronym
AEX
Enrollment
16
Registered
2022-10-10
Start date
2022-09-15
Completion date
2023-09-01
Last updated
2023-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammation

Keywords

Exercise, Cytokines, Leukocytes, Interleukin-10, Interleukin-6

Brief summary

The immune system helps prevent illness, fights off infections, and repairs damaged tissues following an injury. However, when immune cells remain active for prolonged periods of time - a state known as chronic inflammation - they can contribute to the development and progression of chronic diseases like heart disease and diabetes. Exercise can reduce the risk of developing many of these diseases and at least part of the health benefits of exercise are due to the ability of exercise to reduce chronic inflammation. The inflammation-lowering effects of exercise are typically captured by measuring hormone-like molecules released from immune cells called cytokines in the blood. In addition to changes in circulating cytokine levels, exercise may also alter how immune cells respond to these cytokines. How exercise intensity (i.e., how hard you are working during exercise) and pattern (i.e., exercising as a long continuous bout or in short intervals) impact the ability of immune cells to respond to cytokines is not well understood. A better understanding of how exercise intensity and pattern of exercise for reducing chronic inflammation may help determine the best types of exercises for improving health and preventing chronic diseases.

Interventions

Participants will perform an acute bout of interval cycling at at 10% of the difference between lactate threshold and VO2peak until an energy expenditure of 350 kcal is achieved. Blood samples will be obtained immediately before and immediately, 30, and 90 minutes after exercise.

OTHERResting (no exercise) control

Participants will remain in a rested state (i.e., no exercise) for the entire session. Blood samples will be obtained at the same time-points as the exercise sessions.

Participants will perform an acute bout of continuous cycling at 70% of the power output at lactate threshold until an energy expenditure of 350 kcal is achieved. Blood samples will be obtained immediately before and immediately, 30, and 90 minutes after exercise.

Participants will perform an acute bout of continuous cycling at 10% of the difference between lactate threshold and VO2peak until an energy expenditure of 350 kcal is achieved. Blood samples will be obtained immediately before and immediately, 30, and 90 minutes after exercise.

Sponsors

University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Repeated measures randomized counterbalanced crossover design

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-35 years of age * Body mass index between 18.5-30 kg/m\^2 * Free of cardiometabolic and autoimmune/inflammatory disease

Exclusion criteria

* Competitive endurance athlete * Cigarette smoker * Currently taking immunomodulatory/anti-inflammatory medications * Currently pregnant

Design outcomes

Primary

MeasureTime frameDescription
IL-10 mediated STAT3 phosphorylationChange from pre-exercise to immediately and 90-min post-exerciseEx vivo leukocyte STAT3 phosphorylation in response to IL-10 treatment

Secondary

MeasureTime frameDescription
IL-6 mediated STAT3 phosphorylationChange from pre-exercise to immediately and 90-min post-exerciseEx vivo leukocyte STAT3 phosphorylation in response to IL-6 treatment
IL-6 mediated TNF-alpha inhibitionChange from pre-exercise to immediately and 90-min post-exerciseEx vivo inhibition of TNF-alpha production in response to IL-6 treatment
Plasma IL-10Change from pre-exercise to immediately, 30-, and 90-min post-exerciseConcentration of IL-10 in plasma samples
IL-10 mediated TNF-alpha inhibitionChange from pre-exercise to immediately and 90-min post-exerciseEx vivo inhibition of TNF-alpha production in response to IL-10 treatment
Plasma TNF-alphaChange from pre-exercise to immediately, 30-, and 90-min post-exerciseConcentration of TNF-alpha in plasma samples
Hematology panelChange from pre-exercise to immediately, 30-, and 90-min post-exerciseComplete blood count
Extracellular vesiclesChange from pre-exercise to immediately, 30-, and 90-min post-exerciseConcentration of extracellular vesicles in plasma
Plasma IL-6Change from pre-exercise to immediately, 30-, and 90-min post-exerciseConcentration of IL-6 in plasma samples

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026