Oxygen uptake kinetics and cardiac output during cycling in females with type 2 diabetes mellitus

University College Dublin (2009) Proc Physiol Soc 15, C85

Oral Communications: Oxygen uptake kinetics and cardiac output during cycling in females with type 2 diabetes mellitus

O. Mac Ananey1, J. Malone1, D. O'Shea2, S. Warmington3, S. Green4, M. Egaña1

1. Physiology, Trinity College Dublin, Co Dublin, Ireland. 2. Endocrinology, St Colmcilles Hospital Loughlinstown, Co Dublin, Ireland. 3. School of Exercise & Nutrition Sciences, Deakin University, Melbourne, Victoria, Australia. 4. Physiology, University of Otago, Dunedin, New Zealand.

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The dynamic response of oxygen uptake during submaximal cycle exercise appears to be slowed in subjects with type 2 diabetes mellitus compared to non-diabetic controls1,2. This slowed VO2 response may be due to slowed responses of cardiac output, limb blood flow and/or oxygen conductance, although human data are lacking. This human study examined the effect of type 2 diabetes mellitus on cardiac output and the dynamic response of VO2 during three intensities of cycling. Nine middle-aged type 2 diabetic and nine healthy non-diabetic females were recruited for the study. Initially, the ventilatory threshold (VT) and peak VO2 were determined using a maximal graded cycle test. Then subjects completed a series of constant-load exercise bouts (7 min long) on separate days, during which the dynamic response of VO2 was assessed three times, and cardiac output once, at each of three intensities (50%VT, 80%VT & 50%[peakVO2-VT]). Cardiac output was recorded by a closed circuit inert gas rebreathing technique at rest and at 30th & 220th sec of the bout. Dynamic response parameters (e.g., time constant) of the VO2 response were determined by fitting a monoexponential function to the VO2 data. Ethical approval was granted by the Trinity College Dublin, Faculty Research Ethics Committee. Results were analyzed using a one-way ANOVA and are shown as mean±SD. The time constant was significantly larger (P<0.05) in the diabetic group compared with the non-diabetic control group at 50% VT (43.9±14.6 s diabetics, 29.3±11.7 s non-diabetic controls) and 80% VT (47±7.8 s diabetics, 35.4±6.3 s non-diabetic controls); but not at 50% [peak VO2-VT] (47.7±10.1 s diabetics, 47.4±6.5 s heavy controls). Cardiac output responses during exercise (both at 30 and 220 s) were not different between the two groups. The results confirm that type 2 diabetes mellitus slows the dynamic response of VO2 during light and moderate exercise in females; but that this is probably not related to a slowed cardiac output.



Where applicable, experiments conform with Society ethical requirements.

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