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Supramaximal Intensity Hypoxic Exercise and Vascular Function Assessment in Mice
Published on: March 15, 2019
Maximal exercise at high altitude does not exacerbate inflammation in the human brain
Hannah G Caldwell1,2, Travis D Gibbons3, Connor A Howe1
1Centre for Heart, Lung and Vascular Health, School of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, BC, Canada.
High altitude exposure did not worsen brain inflammation after maximal exercise. Maximal exercise induced a net release of specific cytokines from the brain, independent of altitude or systemic inflammation.
Area of Science:
- Exercise Physiology
- Neuroinflammation
- High Altitude Physiology
Background:
- The impact of high altitude (HA) on neuroinflammation and how exercise affects this response remain unclear.
- Previous research has yielded equivocal findings regarding neuroinflammation at HA.
Purpose of the Study:
- To investigate whether maximal exercise at HA exacerbates the neuroinflammatory response.
- To determine the effect of acclimatization to HA on brain cytokine exchange during maximal exercise.
Main Methods:
- Healthy adults (n=12) underwent maximal exercise tests at sea level and HA (3800m).
- Trans-cerebral cytokine exchange was assessed using arterial and internal jugular venous blood sampling.
- Blood flow was measured to calculate cytokine uptake/release by the brain at rest and post-maximal exercise.
Main Results:
- Resting cerebral cytokine exchange was similar between sea level and HA.
- Maximal exercise increased systemic leucocytes at both altitudes.
- A net release of interleukin-6, interleukin-8, monocyte chemoattractant protein-1, and macrophage inflammatory protein-1 beta from the brain occurred post-exercise, independent of altitude.
Conclusions:
- Partial acclimatization to 3800m does not alter the physiological release of cytokines from the brain in response to maximal exercise.
- The adaptive physiological response to maximal exercise involves net cytokine release from the brain, irrespective of HA exposure or systemic inflammation.
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