TY - JOUR
T1 - Relationship between muscle venous blood oxygenation and near-infrared spectroscopy
T2 - quantitative analysis of the Hb and Mb contributions
AU - Koirala, Bhabuk
AU - Concas, Alessandro
AU - Sun, Yi
AU - Gladden, L. Bruce
AU - Lai, Nicola
N1 - Publisher Copyright:
© 2023 American Physiological Society. All rights reserved.
PY - 2023/5
Y1 - 2023/5
N2 - A linear relationship between skeletal muscle venous (CTven) and oxygenated (DHbMbO2,N) or deoxygenated (DHHbMbN) near-infrared spectroscopy (NIRS) signals suggest a main hemoglobin (Hb) contribution to the NIRS signal. However, experimental, and computational evidence supports a significant contribution of myoglobin (Mb) to the NIRS. Venous and NIRS measurements from a canine model of muscle oxidative metabolism (Sun Y, Ferguson BS, Rogatzki MJ, McDonald JR, Gladden LB. Med Sci Sports Exerc 48(10):2013–2020, 2016) were integrated into a computational model of muscle O2 transport and utilization to evaluate whether the relationship between venous and NIRS oxygenation can be affected by a significant Mb contribution to the NIRS signals. The mathematical model predicted well the measure of the changes of CTven and NIRS signals for different O2 delivery conditions (blood flow, arterial O2 content) in muscle at rest (T1, T2) and during contraction (T3). Furthermore, computational analysis indicates that for adequate O2 delivery, Mb contribution to NIRS signals was significant (20%–30%) even in the presence of a linear CTven-NIRS relationship; for a reduced O2 delivery the nonlinearity of the CTven-NIRS relationship was related to the Mb contribution (50%). In this case (T3), the deviation from linearity is observed when O2 delivery is reduced from 1.3 to 0.7 L kg–1·min–1 (CTven < 10 mLO2 100 mL–1) and Mb saturation decreased from 85% to 40% corresponding to an increase of the Mb contribution to DHHbMbN from 15% to 50% and the contribution to DHbMbO2,N from 0% to 30%. In contrast to a common assumption, our model indicates that both NIRS signals (DHHbMbN and DHbMbO2,N are significantly affected by Hb and Mb oxygenation changes.
AB - A linear relationship between skeletal muscle venous (CTven) and oxygenated (DHbMbO2,N) or deoxygenated (DHHbMbN) near-infrared spectroscopy (NIRS) signals suggest a main hemoglobin (Hb) contribution to the NIRS signal. However, experimental, and computational evidence supports a significant contribution of myoglobin (Mb) to the NIRS. Venous and NIRS measurements from a canine model of muscle oxidative metabolism (Sun Y, Ferguson BS, Rogatzki MJ, McDonald JR, Gladden LB. Med Sci Sports Exerc 48(10):2013–2020, 2016) were integrated into a computational model of muscle O2 transport and utilization to evaluate whether the relationship between venous and NIRS oxygenation can be affected by a significant Mb contribution to the NIRS signals. The mathematical model predicted well the measure of the changes of CTven and NIRS signals for different O2 delivery conditions (blood flow, arterial O2 content) in muscle at rest (T1, T2) and during contraction (T3). Furthermore, computational analysis indicates that for adequate O2 delivery, Mb contribution to NIRS signals was significant (20%–30%) even in the presence of a linear CTven-NIRS relationship; for a reduced O2 delivery the nonlinearity of the CTven-NIRS relationship was related to the Mb contribution (50%). In this case (T3), the deviation from linearity is observed when O2 delivery is reduced from 1.3 to 0.7 L kg–1·min–1 (CTven < 10 mLO2 100 mL–1) and Mb saturation decreased from 85% to 40% corresponding to an increase of the Mb contribution to DHHbMbN from 15% to 50% and the contribution to DHbMbO2,N from 0% to 30%. In contrast to a common assumption, our model indicates that both NIRS signals (DHHbMbN and DHbMbO2,N are significantly affected by Hb and Mb oxygenation changes.
KW - contraction
KW - convection
KW - diffusion
KW - hyperoxia
KW - modeling
KW - transport
UR - https://www.scopus.com/pages/publications/85152628611
U2 - 10.1152/japplphysiol.00406.2022
DO - 10.1152/japplphysiol.00406.2022
M3 - 文章
C2 - 36927143
AN - SCOPUS:85152628611
SN - 8750-7587
VL - 134
SP - 1063
EP - 1074
JO - Journal of Applied Physiology
JF - Journal of Applied Physiology
IS - 5
ER -