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临床试验/NCT05574413
NCT05574413已完成不适用

Impact of Acute Exercise Intensity and Pattern on Cytokine Function

University of British Columbia1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2022年9月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1
主要终点
IL-10 mediated STAT3 phosphorylation

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

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

排除标准

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

研究组 & 干预措施

Resting (no exercise) control

Placebo Comparator

Resting (no exercise) control condition

干预措施: Resting (no exercise) control (Other)

Moderate intensity continuous exercise (MICE)

Experimental

Experimental session involving an acute bout of moderate intensity continuous exercise (MICE; continous cycling expending 350 kcal at 70% of lactate threshold)

干预措施: Moderate intensity continuous exercise (Other)

High intensity continuous exercise (HICE)

Experimental

Experimental session involving an acute bout of high intensity continuous exercise (HICE; continuous cycling expending 350 kcal at 10% of the difference between lactate threshold and VO2peak)

干预措施: High intensity continuous exercise (Other)

High intensity interval exercise (HIIT)

Experimental

Experimental session involving an acute bout of high intensity interval exercise (HIIT; cycling intervals expending 350 kcal at 10% of the difference between lactate threshold and VO2peak)

干预措施: High intensity interval exercise (Other)

结局指标

主要结局

IL-10 mediated STAT3 phosphorylation

时间窗: Change from pre-exercise to immediately and 90-min post-exercise

Ex vivo leukocyte STAT3 phosphorylation in response to IL-10 treatment

次要结局

  • Plasma IL-10(Change from pre-exercise to immediately, 30-, and 90-min post-exercise)
  • IL-10 mediated TNF-alpha inhibition(Change from pre-exercise to immediately and 90-min post-exercise)
  • IL-6 mediated STAT3 phosphorylation(Change from pre-exercise to immediately and 90-min post-exercise)
  • Plasma TNF-alpha(Change from pre-exercise to immediately, 30-, and 90-min post-exercise)
  • Hematology panel(Change from pre-exercise to immediately, 30-, and 90-min post-exercise)
  • IL-6 mediated TNF-alpha inhibition(Change from pre-exercise to immediately and 90-min post-exercise)
  • Plasma IL-6(Change from pre-exercise to immediately, 30-, and 90-min post-exercise)
  • Extracellular vesicles(Change from pre-exercise to immediately, 30-, and 90-min post-exercise)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jonathan Little

Professor

University of British Columbia

研究点 (1)

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