H. Theilen et al., CAPILLARY PERFUSION DURING INCOMPLETE FOREBRAIN ISCHEMIA AND REPERFUSION IN RAT-BRAIN, The American journal of physiology, 265(2), 1993, pp. 80000642-80000648
Previous studies have shown a complete plasma perfusion of all capilla
ries in the rat brain under normal physiological conditions. This rais
es the question under which experimental conditions nonperfused capill
aries may show up in the brain. Two experimental models were investiga
ted in rats. 1) Reduced cerebral blood flow (CBF) during incomplete fo
rebrain ischemia: hemorrhagic hypotension was maintained for 30 min at
a mean arterial blood pressure of 41 mmHg. During the final 5 min of
hypotension both carotid arteries were ligated. 2) Reperfusion after i
ncomplete forebrain ischemia: reperfusion lasted for 4 h after either
15 or 30 min of incomplete forebrain ischemia. Under both experimental
conditions, the density of the existing as well as the plasma-perfuse
d brain capillary network was quantified using fluorescent double stai
ning. Local CBF was measured during incomplete forebrain ischemia usin
g the quantitative autoradiographic 4-iodo-[N-methyl-C-14]antipyrine t
echnique. The results showed a decrease in CBF during incomplete foreb
rain ischemia, which amounted up to 94%. Whereas normotensive control
animals showed a complete staining of all capillaries within 5 s after
the intravenous injection of Evans blue, this period of time was incr
eased to 10 s during incomplete forebrain ischemia, indicating a delay
ed capillary perfusion. Four hours of reperfusion after 15 min of inco
mplete forebrain ischemia resulted in a complete capillary staining, w
hereas reperfusion after 30 min of ischemia was followed by intracereb
ral bleedings and a few nonperfused capillary areas (circulation time
of Evans blue: 10 s). The data show 1) during incomplete forebrain isc
hemia, which was verified by a drastic reduction of CBF, all brain cap
illaries investigated remained perfused with plasma, although at a low
ered velocity; 2) during reperfusion occasional perfusion deficits sho
wed up.