A comparison of the microcirculation in the rat spinotrapezius and diaphragm muscles.

Of all skeletal muscles examined in the rat, the spinotrapezius (S) and diaphragm (D) have the closest fiber-type composition. However, their oxidative capacities differ by two- to threefold. We have developed an intravital microscopy preparation to study diaphragm microcirculation in vivo. Using this preparation and the standard spinotrapezius model first described by S. D. Gray (1973, Microvasc. Res. 5, 395-400), we tested the hypothesis that pronounced microcirculatory differences would exist between these two muscles as a function of their disparate oxidative capacities. The lineal density of all capillaries in the spinotrapezius was 33.6 +/- 1.5 compared to 65.1 +/- 3.3 capillaries/mm in the diaphragm (P < 0.001). In the diaphragm compared with the spinotrapezius muscle, a significantly (P < 0.05) greater proportion of capillary countercurrent flow (D, 29 +/- 6% vs 8 +/- 6%) existed. Within both muscles, there was a similar proportion of capillaries supporting red blood cell (RBC) flow (S, 89 +/- 7% vs D, 92 +/- 2%). However, the diaphragm supported significantly (P < 0.001) greater intracapillary RBC velocities (D, 302 +/- 11 vs S, 226 +/- 9 micron/s) and fluxes (D, 33.4 +/- 1.1 vs S, 19.2 +/- 2.1 cells/s) compared with the spinotrapezius. Capillary "tube" hematocrit was greater (P = 0.01) in the diaphragm (0.32 +/- 0.02) than in the spinotrapezius (0.22 +/- 0.03) muscle. These data demonstrate that microcirculatory flow characteristics in resting muscle can be regulated independent of muscle fiber-type composition and may be related to muscle oxidative capacity.

[1]  D. Poole,et al.  Skeletal muscle microcirculatory structure and hemodynamics in diabetes. , 1998, Respiration physiology.

[2]  C. Ellis,et al.  Muscle capillary-to-fiber perimeter ratio: morphometry. , 1991, The American journal of physiology.

[3]  B. Duling,et al.  Direct measurement of microvessel hematocrit, red cell flux, velocity, and transit time. , 1982, The American journal of physiology.

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

[5]  R. Armstrong,et al.  A method for using microspheres to measure muscle blood flow in exercising rats. , 1982, Journal of applied physiology: respiratory, environmental and exercise physiology.

[6]  C. Ranke,et al.  Distribution of local oxygen consumption in resting skeletal muscle. , 1985, Advances in experimental medicine and biology.

[7]  B. Duling,et al.  Determination of capillary tube hematocrit during arteriolar microperfusion. , 1994, The American journal of physiology.

[8]  K. Rakušan,et al.  Capillary length, tortuosity, and spacing in rat myocardium during cardiac cycle. , 1992, The American journal of physiology.

[9]  C. Desjardins,et al.  Heparinase treatment suggests a role for the endothelial cell glycocalyx in regulation of capillary hematocrit. , 1990, The American journal of physiology.

[10]  S. Gray Rat spinotrapezius muscle preparation for microscopic observation of the terminal vascular bed. , 1973, Microvascular research.

[11]  K. Groebe,et al.  Calculated intra- and extracellular PO2 gradients in heavily working red muscle. , 1990, The American journal of physiology.

[12]  J. Piiper,et al.  Significance of the Bohr effect for tissue oxygenation in a model with counter-current blood flow. , 1989, Respiration physiology.

[13]  J. Barberà,et al.  Effects of training on muscle O2 transport at VO2max. , 1992, Journal of applied physiology.

[14]  J. E. McKenzie,et al.  Resting blood flow and oxygen consumption in soleus and gracilis muscles of cats. , 1980, The American journal of physiology.

[15]  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.

[16]  G. Schmid-Schönbein,et al.  Temporal correlation between maximum tetanic force and cell death in postischemic rat skeletal muscle. , 1995, The Journal of clinical investigation.

[17]  I. Silver,et al.  Effect of oxygen tension on cellular energetics. , 1977, The American journal of physiology.

[18]  D. Poole,et al.  Capillary and fiber geometry in rat diaphragm perfusion fixed in situ at different sarcomere lengths. , 1992, Journal of applied physiology.

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

[20]  D. Reis,et al.  Differences in nutrient blood flow of red and white skeletal muscle in the cat. , 1967, The American journal of physiology.

[21]  D. Poole,et al.  In vivo microvascular structural and functional consequences of muscle length changes. , 1997, The American journal of physiology.

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

[23]  D. Poole,et al.  Blood flow response to treadmill running in the rat spinotrapezius muscle. , 1996, The American journal of physiology.

[24]  Philip L. Altman,et al.  Biology Data Book , 1975 .

[25]  B. Folkow,et al.  A comparison between “red” and “white” muscle with respect to blood supply, capillary surface area and oxygen uptake during rest and exercise , 1968 .

[26]  R. Crystal,et al.  The Lung: Scientific Foundations , 1991 .

[27]  H. Bohlen,et al.  Functional adaptations of rat skeletal muscle arterioles to aerobic exercise training. , 1992, Journal of applied physiology.

[28]  K. Rakušan,et al.  Microvascular flow vectors in normal and hypertrophic myocardium as determined by the method of colored microspheres. , 1992, Microvascular research.

[29]  O. Hudlická Uptake of substrates in slow and fast muscles in situ. , 1975, Microvascular research.

[30]  E. Vicaut,et al.  A preparation for in vivo study of the diaphragmatic microcirculation in the rat. , 1990, Microvascular research.

[31]  R. Armstrong,et al.  Design of the mammalian respiratory system. VI Distribution of mitochondria and capillaries in various muscles. , 1981, Respiration physiology.

[32]  O. Mathieu‐costello Capillary tortuosity and degree of contraction or extension of skeletal muscles. , 1987, Microvascular research.

[33]  O. Hudlická,et al.  A comparison of the microcirculation in rat fast glycolytic and slow oxidative muscles at rest and during contractions. , 1987, Microvascular research.

[34]  M. Delp,et al.  Composition and size of type I, IIA, IID/X, and IIB fibers and citrate synthase activity of rat muscle. , 1996, Journal of applied physiology.

[35]  O. Mathieu‐costello,et al.  Relationship Between Fiber Capillarization and Mitochondrial Volume Density in Control and Trained Rat Soleus and Plantaris Muscles , 1996, Microcirculation.

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

[37]  J. Petrofsky,et al.  Blood flow and metabolism during isometric contractions in cat skeletal muscle. , 1981, Journal of applied physiology: respiratory, environmental and exercise physiology.

[38]  D. Welsh,et al.  Muscle length directs sympathetic nerve activity and vasomotor tone in resistance vessels of hamster retractor. , 1996, Circulation research.

[39]  S. Powers,et al.  Diaphragm structure and function in health and disease. , 1997, Medicine and science in sports and exercise.