Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure

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Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure. / Hartmann, Jacob Peter; Dahl, Rasmus H.; Nymand, Stine; Munch, Gregers W.; Ryrsø, Camilla K.; Pedersen, Bente K.; Thaning, Pia; Mortensen, Stefan P.; Berg, Ronan M.G.; Iepsen, Ulrik Winning.

In: Frontiers in Physiology, Vol. 13, 979359, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Hartmann, JP, Dahl, RH, Nymand, S, Munch, GW, Ryrsø, CK, Pedersen, BK, Thaning, P, Mortensen, SP, Berg, RMG & Iepsen, UW 2022, 'Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure', Frontiers in Physiology, vol. 13, 979359. https://doi.org/10.3389/fphys.2022.979359

APA

Hartmann, J. P., Dahl, R. H., Nymand, S., Munch, G. W., Ryrsø, C. K., Pedersen, B. K., Thaning, P., Mortensen, S. P., Berg, R. M. G., & Iepsen, U. W. (2022). Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure. Frontiers in Physiology, 13, [979359]. https://doi.org/10.3389/fphys.2022.979359

Vancouver

Hartmann JP, Dahl RH, Nymand S, Munch GW, Ryrsø CK, Pedersen BK et al. Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure. Frontiers in Physiology. 2022;13. 979359. https://doi.org/10.3389/fphys.2022.979359

Author

Hartmann, Jacob Peter ; Dahl, Rasmus H. ; Nymand, Stine ; Munch, Gregers W. ; Ryrsø, Camilla K. ; Pedersen, Bente K. ; Thaning, Pia ; Mortensen, Stefan P. ; Berg, Ronan M.G. ; Iepsen, Ulrik Winning. / Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure. In: Frontiers in Physiology. 2022 ; Vol. 13.

Bibtex

@article{62a23db87f284401aa909657b23505c5,
title = "Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure",
abstract = "Aim: Skeletal muscle convective and diffusive oxygen (O2) transport are peripheral determinants of exercise capacity in both patients with chronic obstructive pulmonary disease (COPD) and chronic heart failure (CHF). We hypothesised that differences in these peripheral determinants of performance between COPD and CHF patients are revealed during small muscle mass exercise, where the cardiorespiratory limitations to exercise are diminished. Methods: Eight patients with moderate to severe COPD, eight patients with CHF (NYHA II), and eight age- and sex-matched controls were studied. We measured leg blood flow ({\.Q}leg) by Doppler ultrasound during submaximal one-legged knee-extensor exercise (KEE), while sampling arterio-venous variables across the leg. The capillary oxyhaemoglobin dissociation curve was reconstructed from paired femoral arterial-venous oxygen tensions and saturations, which enabled the estimation of O2 parameters at the microvascular level within skeletal muscle, so that skeletal muscle oxygen conductance (DSMO2) could be calculated and adjusted for flow (DSMO2/{\.Q}leg) to distinguish convective from diffusive oxygen transport. Results: During KEE, {\.Q}leg increased to a similar extent in CHF (2.0 (0.4) L/min) and controls (2.3 (0.3) L/min), but less in COPD patients (1.8 (0.3) L/min) (p <0.03). There was no difference in resting DSMO2 between COPD and CHF and when adjusting for flow, the DSMO2 was higher in both groups compared to controls (COPD: 0.97 (0.23) vs. controls 0.63 (0.24) mM/kPa, p= 0.02; CHF 0.98 (0.11) mM/kPa vs. controls, p= 0.001). The {\.Q}-adjusted DSMO2 was not different in COPD and CHF during KEE (COPD: 1.19 (0.11) vs. CHF: 1.00 (0.18) mM/kPa; p= 0.24) but higher in COPD vs. controls: 0.87 (0.28) mM/kPa (p= 0.02), and only CHF did not increase {\.Q}-adjusted DSMO2 from rest (p= 0.2). Conclusion: Disease-specific factors may play a role in peripheral exercise limitation in patients with COPD compared with CHF. Thus, low convective O2 transport to contracting muscle seemed to predominate in COPD, whereas muscle diffusive O2 transport was unresponsive in CHF.",
keywords = "capillary recruitment, chronic obstructive pulmonary disease, COPD, exercise capacity, heart failiure, knee extensor exercise",
author = "Hartmann, {Jacob Peter} and Dahl, {Rasmus H.} and Stine Nymand and Munch, {Gregers W.} and Ryrs{\o}, {Camilla K.} and Pedersen, {Bente K.} and Pia Thaning and Mortensen, {Stefan P.} and Berg, {Ronan M.G.} and Iepsen, {Ulrik Winning}",
note = "Publisher Copyright: Copyright {\textcopyright} 2022 Hartmann, Dahl, Nymand, Munch, Ryrs{\o}, Pedersen, Thaning, Mortensen, Berg and Iepsen.",
year = "2022",
doi = "10.3389/fphys.2022.979359",
language = "English",
volume = "13",
journal = "Frontiers in Physiology",
issn = "1664-042X",
publisher = "Frontiers Media S.A.",

}

RIS

TY - JOUR

T1 - Regulation of the microvasculature during small muscle mass exercise in chronic obstructive pulmonary disease vs. chronic heart failure

AU - Hartmann, Jacob Peter

AU - Dahl, Rasmus H.

AU - Nymand, Stine

AU - Munch, Gregers W.

AU - Ryrsø, Camilla K.

AU - Pedersen, Bente K.

AU - Thaning, Pia

AU - Mortensen, Stefan P.

AU - Berg, Ronan M.G.

AU - Iepsen, Ulrik Winning

N1 - Publisher Copyright: Copyright © 2022 Hartmann, Dahl, Nymand, Munch, Ryrsø, Pedersen, Thaning, Mortensen, Berg and Iepsen.

PY - 2022

Y1 - 2022

N2 - Aim: Skeletal muscle convective and diffusive oxygen (O2) transport are peripheral determinants of exercise capacity in both patients with chronic obstructive pulmonary disease (COPD) and chronic heart failure (CHF). We hypothesised that differences in these peripheral determinants of performance between COPD and CHF patients are revealed during small muscle mass exercise, where the cardiorespiratory limitations to exercise are diminished. Methods: Eight patients with moderate to severe COPD, eight patients with CHF (NYHA II), and eight age- and sex-matched controls were studied. We measured leg blood flow (Q̇leg) by Doppler ultrasound during submaximal one-legged knee-extensor exercise (KEE), while sampling arterio-venous variables across the leg. The capillary oxyhaemoglobin dissociation curve was reconstructed from paired femoral arterial-venous oxygen tensions and saturations, which enabled the estimation of O2 parameters at the microvascular level within skeletal muscle, so that skeletal muscle oxygen conductance (DSMO2) could be calculated and adjusted for flow (DSMO2/Q̇leg) to distinguish convective from diffusive oxygen transport. Results: During KEE, Q̇leg increased to a similar extent in CHF (2.0 (0.4) L/min) and controls (2.3 (0.3) L/min), but less in COPD patients (1.8 (0.3) L/min) (p <0.03). There was no difference in resting DSMO2 between COPD and CHF and when adjusting for flow, the DSMO2 was higher in both groups compared to controls (COPD: 0.97 (0.23) vs. controls 0.63 (0.24) mM/kPa, p= 0.02; CHF 0.98 (0.11) mM/kPa vs. controls, p= 0.001). The Q̇-adjusted DSMO2 was not different in COPD and CHF during KEE (COPD: 1.19 (0.11) vs. CHF: 1.00 (0.18) mM/kPa; p= 0.24) but higher in COPD vs. controls: 0.87 (0.28) mM/kPa (p= 0.02), and only CHF did not increase Q̇-adjusted DSMO2 from rest (p= 0.2). Conclusion: Disease-specific factors may play a role in peripheral exercise limitation in patients with COPD compared with CHF. Thus, low convective O2 transport to contracting muscle seemed to predominate in COPD, whereas muscle diffusive O2 transport was unresponsive in CHF.

AB - Aim: Skeletal muscle convective and diffusive oxygen (O2) transport are peripheral determinants of exercise capacity in both patients with chronic obstructive pulmonary disease (COPD) and chronic heart failure (CHF). We hypothesised that differences in these peripheral determinants of performance between COPD and CHF patients are revealed during small muscle mass exercise, where the cardiorespiratory limitations to exercise are diminished. Methods: Eight patients with moderate to severe COPD, eight patients with CHF (NYHA II), and eight age- and sex-matched controls were studied. We measured leg blood flow (Q̇leg) by Doppler ultrasound during submaximal one-legged knee-extensor exercise (KEE), while sampling arterio-venous variables across the leg. The capillary oxyhaemoglobin dissociation curve was reconstructed from paired femoral arterial-venous oxygen tensions and saturations, which enabled the estimation of O2 parameters at the microvascular level within skeletal muscle, so that skeletal muscle oxygen conductance (DSMO2) could be calculated and adjusted for flow (DSMO2/Q̇leg) to distinguish convective from diffusive oxygen transport. Results: During KEE, Q̇leg increased to a similar extent in CHF (2.0 (0.4) L/min) and controls (2.3 (0.3) L/min), but less in COPD patients (1.8 (0.3) L/min) (p <0.03). There was no difference in resting DSMO2 between COPD and CHF and when adjusting for flow, the DSMO2 was higher in both groups compared to controls (COPD: 0.97 (0.23) vs. controls 0.63 (0.24) mM/kPa, p= 0.02; CHF 0.98 (0.11) mM/kPa vs. controls, p= 0.001). The Q̇-adjusted DSMO2 was not different in COPD and CHF during KEE (COPD: 1.19 (0.11) vs. CHF: 1.00 (0.18) mM/kPa; p= 0.24) but higher in COPD vs. controls: 0.87 (0.28) mM/kPa (p= 0.02), and only CHF did not increase Q̇-adjusted DSMO2 from rest (p= 0.2). Conclusion: Disease-specific factors may play a role in peripheral exercise limitation in patients with COPD compared with CHF. Thus, low convective O2 transport to contracting muscle seemed to predominate in COPD, whereas muscle diffusive O2 transport was unresponsive in CHF.

KW - capillary recruitment

KW - chronic obstructive pulmonary disease

KW - COPD

KW - exercise capacity

KW - heart failiure

KW - knee extensor exercise

UR - http://www.scopus.com/inward/record.url?scp=85138280478&partnerID=8YFLogxK

U2 - 10.3389/fphys.2022.979359

DO - 10.3389/fphys.2022.979359

M3 - Journal article

C2 - 36134330

AN - SCOPUS:85138280478

VL - 13

JO - Frontiers in Physiology

JF - Frontiers in Physiology

SN - 1664-042X

M1 - 979359

ER -

ID: 321169482