Assessment and impact of heterogeneities of convective oxygen transport parameters in capillaries of striated muscle: experimental and theoretical.

Convective oxygen transport parameters were determined in arteriolar (n = 5) and venular (n = 5) capillary networks in the hamster cheek pouch retractor muscle. Simultaneously determined values of red blood cell velocity, lineal density, red blood cell frequency, hemoglobin oxygen saturation (SO2), oxygen flow (QO2), longitudinal SO2 gradient, and diameter were obtained in a total of 73 capillaries, 39 at the arteriolar ends of the network (arteriolar capillaries) and 34 at the venular ends (venular capillaries). We found that the hemodynamic variables were not different at the two ends. However, not unexpectedly, SO2 and QO2 were significantly higher at the upstream end of arteriolar capillaries (60.8 +/- 9.8 (SD)% and 0.150 +/- 0.081 pl/sec, respectively) compared with the downstream end of venular capillaries (39.9 +/- 13.6% and 0.108 +/- 0.095 pl/sec, respectively). Heterogeneities in red blood cell velocity, lineal density, SO2, and QO2, assessed by their coefficients of variation, were significantly greater in venular capillaries. To evaluate the impact of these heterogeneities on oxygen exchange, we incorporated these unique experimental data into a mathematical model of oxygen transport which accounts for variability in red blood cell frequency, lineal density, inlet SO2, capillary diameter, and, to some degree, capillary flow path lengths. An unexpected result of the simulation is that only the incorporation of variability in capillary flow path lengths had any marked effect on the heterogeneity in end-capillary SO2 in resting muscle due to extensive diffusional shunting of oxygen among adjacent capillaries. We subsequently evaluated, through model simulations, the effect of these heterogeneities under conditions of increased flow and high oxygen consumption. Under these conditions, the model predicts that heterogeneities in the hemodynamic parameters will have a marked effect on oxygen transport in this muscle.

[1]  C G Ellis,et al.  Measurement of hemoglobin oxygen saturation in capillaries. , 1987, The American journal of physiology.

[2]  A. Groom,et al.  Regulation of blood flow in individual capillaries of resting skeletal muscle in frogs. , 1980, Microvascular research.

[3]  Measurements of oxygen transport in single capillaries. , 1983, Advances in experimental medicine and biology.

[4]  A. Popel,et al.  A theoretical analysis of the effect of the particulate nature of blood on oxygen release in capillaries. , 1986, Microvascular research.

[5]  I. Sarelius Cell flow path influences transit time through striated muscle capillaries. , 1986, The American journal of physiology.

[6]  E. Bockman Blood flow and oxygen consumption in active soleus and gracilis muscles in cats. , 1983, American Journal of Physiology.

[7]  B. Duling,et al.  Microvascular hematocrit and red cell flow in resting and contracting striated muscle. , 1979, The American journal of physiology.

[8]  G. Gutierrez,et al.  The rate of oxygen release and its effect on capillary O2 tension: a mathematical analysis. , 1986, Respiration physiology.

[9]  R. Pittman,et al.  In vitro O2 uptake and histochemical fiber type of resting hamster muscles. , 1984, Journal of applied physiology: respiratory, environmental and exercise physiology.

[10]  Honig Cr,et al.  Correlation of O2 transport on the micro and macro scale. , 1982 .

[11]  G. R. Kelman,et al.  Digital computer subroutine for the conversion of oxygen tension into saturation. , 1966, Journal of applied physiology.

[12]  M. L. Ellsworth,et al.  Heterogeneity of oxygen diffusion through hamster striated muscles. , 1984, The American journal of physiology.

[13]  B. Duling,et al.  Evidence that capillary perfusion heterogeneity is not controlled in striated muscle. , 1985, The American journal of physiology.

[14]  G. Cokelet,et al.  Oxygen delivery from red cells. , 1985, Biophysical journal.

[15]  E. M. Slayter Optical methods in biology , 1970 .

[16]  E. Homsher,et al.  Reappraisal of diffusion, solubility, and consumption of oxygen in frog skeletal muscle, with applications to muscle energy balance , 1985, The Journal of general physiology.

[17]  C. Ellis,et al.  Temporal and spatial distributions of red cell velocity in capillaries of resting skeletal muscle, including estimates of red cell transit times. , 1981, Microvascular research.

[18]  R. Pittman,et al.  Hamster retractor muscle: a new preparation for intravital microscopy. , 1982, Microvascular research.

[19]  Measurement of the lineal density of red blood cells in capillaries in vivo, using a computerized frame-by-frame analysis of video images. , 1984, Microvascular research.

[20]  P. Johnson,et al.  Capillary network geometry and red cell distribution in hamster cremaster muscle. , 1982, The American journal of physiology.

[21]  A. Popel,et al.  Effect of Heterogeneous Oxygen Delivery on the Oxygen Distribution in Skeletal Muscle. , 1986, Mathematical biosciences.

[22]  A method for on-line measurements of red cell velocity in microvessels using computerized frame-by-frame analysis of television images. , 1980, Microvascular research.

[23]  Y. Cassuto,et al.  Haematological Changes in Heat‐Acclimated Golden Hamsters , 1970, British journal of haematology.

[24]  B. Duling,et al.  Microvascular adaptations during maturation of striated muscle. , 1981, The American journal of physiology.

[25]  B. Duling,et al.  Distribution of capillary blood flow in the microcirculation of the hamster: an in vivo study using epifluorescent microscopy. , 1984, Microvascular research.