TY - JOUR
T1 - Priming exercise accelerates oxygen uptake kinetics during high-intensity cycle exercise in middle-aged individuals with type 2 diabetes
AU - Rocha, J.
AU - Gildea, N.
AU - O’Shea, D.
AU - Green, Simon
AU - Egaña, M.
N1 - Publisher Copyright:
Copyright © 2022 Rocha, Gildea, O’Shea, Green and Egaña.
PY - 2022/11/18
Y1 - 2022/11/18
N2 - Background: The primary phase time constant of pulmonary oxygen uptake kinetics ((Formula presented.) τp) during submaximal efforts is longer in middle-aged people with type 2 diabetes (T2D), partly due to limitations in oxygen supply to active muscles. This study examined if a high-intensity “priming” exercise (PE) would speed (Formula presented.) τp during a subsequent high-intensity cycling exercise in T2D due to enhanced oxygen delivery. Methods: Eleven (4 women) middle-aged individuals with type 2 diabetes and 11 (4 women) non-diabetic controls completed four separate cycling bouts each starting at an ‘unloaded’ baseline of 10 W and transitioning to a high-intensity constant-load. Two of the four cycling bouts were preceded by priming exercise. The dynamics of pulmonary (Formula presented.) and muscle deoxygenation (i.e. deoxygenated haemoglobin and myoglobin concentration [HHb + Mb]), were calculated from breath-by-breath and near-infrared spectroscopy data at the vastus lateralis, respectively. Results: At baseline (Formula presented.) τp, was slower (p < 0.001) in the type 2 diabetes group (48 ± 6 s) compared to the control group (34 ± 2 s) but priming exercise significantly reduced (Formula presented.) τp (p < 0.001) in type 2 diabetes (32 ± 6 s) so that post priming exercise it was not different compared with controls (34 ± 3 s). Priming exercise reduced the amplitude of the (Formula presented.) slow component (As) in both groups (type 2 diabetes: 0.26 ± 0.11 to 0.16 ± 0.07 L/min; control: 0.33 ± 0.13 to 0.25 ± 0.14 L/min, p < 0.001), while [HHb + Mb] kinetics remained unchanged. Conclusion: These results suggest that in middle-aged men and women with T2D, PE speeds (Formula presented.) τp likely by a better matching of O2 delivery to utilisation and reduces the (Formula presented.) As during a subsequent high-intensity exercise.
AB - Background: The primary phase time constant of pulmonary oxygen uptake kinetics ((Formula presented.) τp) during submaximal efforts is longer in middle-aged people with type 2 diabetes (T2D), partly due to limitations in oxygen supply to active muscles. This study examined if a high-intensity “priming” exercise (PE) would speed (Formula presented.) τp during a subsequent high-intensity cycling exercise in T2D due to enhanced oxygen delivery. Methods: Eleven (4 women) middle-aged individuals with type 2 diabetes and 11 (4 women) non-diabetic controls completed four separate cycling bouts each starting at an ‘unloaded’ baseline of 10 W and transitioning to a high-intensity constant-load. Two of the four cycling bouts were preceded by priming exercise. The dynamics of pulmonary (Formula presented.) and muscle deoxygenation (i.e. deoxygenated haemoglobin and myoglobin concentration [HHb + Mb]), were calculated from breath-by-breath and near-infrared spectroscopy data at the vastus lateralis, respectively. Results: At baseline (Formula presented.) τp, was slower (p < 0.001) in the type 2 diabetes group (48 ± 6 s) compared to the control group (34 ± 2 s) but priming exercise significantly reduced (Formula presented.) τp (p < 0.001) in type 2 diabetes (32 ± 6 s) so that post priming exercise it was not different compared with controls (34 ± 3 s). Priming exercise reduced the amplitude of the (Formula presented.) slow component (As) in both groups (type 2 diabetes: 0.26 ± 0.11 to 0.16 ± 0.07 L/min; control: 0.33 ± 0.13 to 0.25 ± 0.14 L/min, p < 0.001), while [HHb + Mb] kinetics remained unchanged. Conclusion: These results suggest that in middle-aged men and women with T2D, PE speeds (Formula presented.) τp likely by a better matching of O2 delivery to utilisation and reduces the (Formula presented.) As during a subsequent high-intensity exercise.
UR - https://hdl.handle.net/1959.7/uws:77463
U2 - 10.3389/fphys.2022.1006993
DO - 10.3389/fphys.2022.1006993
M3 - Article
SN - 1664-042X
VL - 13
JO - Frontiers in Physiology
JF - Frontiers in Physiology
M1 - 1006993
ER -