Effect of different levels of acute hypoxia on subsequent oral glucose tolerance in males with overweight: A balanced cross‐over pilot feasibility study

Author:

Corbett Jo1ORCID,Tipton Michael J.1,Perissiou Maria2,James Thomas12,Young John S.34,Newman Alexander3,Cummings Michael5,Montgomery Hugh6,Grocott Michael P. W.7ORCID,Shepherd Anthony I.25

Affiliation:

1. Extreme Environments Laboratory, School of Sport, Health and Exercise Science University of Portsmouth Portsmouth UK

2. Clinical, Health and Rehabilitation Team, School of Sport, Health and Exercise Science University of Portsmouth Portsmouth UK

3. National Horizons Centre Teesside University Middlesbrough UK

4. School of Health and Life Sciences Teesside University Middlesbrough UK

5. Diabetes and Endocrinology Department Portsmouth Hospitals University NHS Trust Portsmouth UK

6. Centre for Sport Exercise and Health, Dept Medicine University College London London UK

7. Perioperative and Critical Care Theme, NIHR Southampton Biomedical Research Centre University Hospital Southampton/University of Southampton Southampton UK

Abstract

AbstractPrevious research has shown that ≤60 min hypoxic exposure improves subsequent glycaemic control, but the optimal level of hypoxia is unknown and data are lacking from individuals with overweight. We undertook a cross‐over pilot feasibility study investigating the effect of 60‐min prior resting exposure to different inspired oxygen fractions (CON FIO2 = 0.209; HIGH FIO2 = 0.155; VHIGH FIO2 = 0.125) on glycaemic control, insulin sensitivity, and oxidative stress during a subsequent oral glucose tolerance test (OGTT) in males with overweight (mean (SD) BMI = 27.6 (1.3) kg/m2; n = 12). Feasibility was defined by exceeding predefined withdrawal criteria for peripheral blood oxygen saturation (SpO2), partial pressure of end‐tidal oxygen or carbon dioxide and acute mountain sickness (AMS), and dyspnoea symptomology. Hypoxia reduced SpO2 in a stepwise manner (CON = 97(1)%; HIGH = 91(1)%; VHIGH = 81(3)%, p < 0.001), but did not affect peak plasma glucose concentration (CON = 7.5(1.8) mmol∙L−1; HIGH = 7.7(1.1) mmol∙L−1; VHIGH = 7.7(1.1) mmol∙L−1; p = 0.777; η2 = 0.013), plasma glucose area under the curve, insulin sensitivity, or metabolic clearance rate of glucose (p > 0.05). We observed no between‐conditions differences in oxidative stress (p > 0.05), but dyspnoea and AMS symptoms increased in VHIGH (p < 0.05), with one participant meeting the withdrawal criteria. Acute HIGH or VHIGH exposure prior to an OGTT does not influence glucose homeostasis in males with overweight, but VHIGH is associated with adverse symptomology and reduced feasibility.

Publisher

Wiley

Subject

Physiology (medical),Physiology

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