Wp. Paaske et P. Sejrsen, MICROVASCULAR FUNCTION IN THE PERIPHERAL VASCULAR BED DURING ISCHEMIAAND OXYGEN-FREE PERFUSION, European journal of vascular and endovascular surgery, 9(1), 1995, pp. 29-37
Objectives: To determine the influence of acute ischaemia and absence
of leukocytes on the microvascular function and capillary permeability
in skeletal muscle. Design: Prospective, open study. Setting: Univers
ity Department of Vascular Surgery and Institute of Medical Physiology
. Materials and Methods: Ten isolated cat gastrocnemius muscles were p
erfused with oxygen-free Ringer-albumin solution through the femoral a
rtery. A 5 mu l bolus with 14.8 MBq Cr-51-EDTA was injected through a
side branch into the femoral artery, and the response function was det
ected over the muscle by a scintillation detector connected to a spect
rometer and a computer. The perfusion coefficient was measured directl
y at the venous outlet. The response function was analysed in accordan
ce with non-compartmental black box kinetic principles to give perfusi
on rate, capillary extraction fraction and capillary diffusional perme
ability-surface area product (PdS). In separate experiments the molecu
lar size and the free diffusion coefficient of Cr-51-EDTA in water at
37 degrees C were determined by a modified true transient diffusion me
thod. Main Results: During perfusion the PdS-product increased as a fu
nction of flow rate, f, in accordance with the linear regression line
PdS = 1.78 + 0.15 f between 5 to 60 ml/100 g/min. This permeative cond
uctance was identical to that found previously in a similar experiment
al set up with oxygenated whole blood perfusion. During oxygen free pe
rfusion the perfusion rate was linear function of arterial perfusion p
ressure, and autoregulation of blood flow did not occur in response to
variations of arterial perfusion pressures. The free diffusion coeffi
cient in water at 37 degrees C Cr-51-EDTA was 7.4 X 10(-6)cm(2)/s (n =
36), which corresponds to a Stokes-Einstein molecular radius, r(SE),
of 0.439 nm. Conclusions: In spite of complete anoxia and absence of n
ormal microcirculatory flow regulating mechanisms there is no sign of
changes in capillary diffusional permeability for smaller hydrophilic
molecules and functional membrane damage is not elicited in the absenc
e of oxygen under these conditions.