Two forms of hypoxia are thought to exist in tumours: (1) hypoxia caus
ed by limitations of its diffusion (chronic hypoxia); and (2) hypoxia
caused by changes in perfusion (acute hypoxia). Indirect information s
uggests the existence of perfusion-limited hypoxia, but there is no di
rect proof that fluctuations in blood dow can lead to hypoxia, nor is
there any information regarding potential causes of fluctuant flow. In
this study, we have begun to explore these questions using R3230AC tu
mours transplanted into rat dorsal-flap window chambers. Two types of
fluctuant flow have been observed. The first type, usually confined to
single vessels, is typified by instability of flow magnitude and dire
ction, and total vascular stasis occurs, but only for a few seconds at
a time (4% incidence). The second type of fluctuation occurs in group
s of vessels and is cyclic, with cycle times ranging from 20-60 min. T
otal vascular stasis does not necessarily occur, but the fluctuations
in red cell flux are accompanied by changes in vascular oxygen content
, as measured by microelectrodes. Another source of chronic hypoxia ha
s also been identified in these experiments. Nine per cent (9%) of ves
sels examined had plasma how, but very low or absent red cell flux ove
r periods of many minutes.