1. In the feet of patients with diabetic neuropathy, total skin blood
flow is increased due to an increased shunt flow. The question is, doe
s this increased anastomotic shunt flow lead to either under- or overp
erfused nutritive capillaries. 2. To solve this question, skin microci
rculation tests of the left big toe were performed in 20 healthy subje
cts and in 40 insulin-dependent patients without macroangiopathy, 20 w
ithout and 20 with neuropathy. Skin temperature measurements and laser
Doppler fluxmetry were performed to record mainly shunt flow and capi
llaroscopy to study nailfold capillary blood flow. 3. The insulin-depe
ndent diabetic patients with neuropathy had a higher baseline skin tem
perature (mean+/-SEM; 30.0+/-0.6 degrees C) and laser Doppler fluxmetr
y [26.2+/-2.2 perfusion units (pu)] than patients without neuropathy (
27.2+/-0.8 degrees C, P <0.01; 16.1+/-2.0 pu, P <0.01) and healthy con
trol subjects (27.9+/-0.7 degrees C, P <0.05; 18.6+/-2.8 pu, P <0.05).
Sympathetic stimulation (inspiratory gasp) resulted in a smaller lase
r Doppler fluxmetry decrease in the neuropathic patients (31.4+/-4.6%)
compared with non-neuropathic patients (48.2+/-5.1%, P <0.05) and con
trol subjects (49.0+/-3.8%, P <0.05), while no difference between the
three groups was seen in the laser Doppler fluxmetry decrease during a
postural vasoconstriction test, The number of visible capillaries was
highest in the neuropathic patients (10.2+/-0.6/0.5 mm(2)), when comp
ared with non-neuropathic patients (8.7+/-1.2/0.5 mm(2), P <0.05) and
control subjects (8.3+/-0.3/0.5 mm(2), P <0.001). Capillary blood-cell
velocity was significantly higher in the neuropathic patients (0.32+/
-0.05 mm/s) compared with non-neuropathic patients (0.23+/-0.03mm/s, P
<0.05) and control subjects (0.23+/-0.02 mm/s, P <0.01). 4. We conclu
de that there is an overperfused nutritive capillary circulation in th
e feet of patients with diabetic neuropathy, This is in contradiction
to the capillary steal phenomenon and favours the hyperdynamic hypothe
sis to explain the decreased healing potential in diabetic neuropathic
foot ulceration.