The effects of hypoxemia on the cerebral vasculature have been describ
ed in animal models, but data from human studies are limited and have
often relied on invasive methodology. The ability to detect a threshol
d for hypoxic vasodilatation in humans may be clinically useful, parti
cularly in patients with impaired intracranial compliance. Because phy
siology may differ among subjects, it would be advantageous to measure
such thresholds using noninvasive bedside techniques that could be re
adily applied to individual patients. We have attempted to identify th
resholds of hypoxic vasodilatation in volunteers using noninvasive met
hods of measurement. Thirteen healthy volunteers were studied using tr
anscranial Doppler sonography. Time-averaged middle cerebral artery ma
ximal flow velocity (MCA FVx), mean arterial blood pressure, periphera
l oxygen saturation (SpO(2)), and partial pressure of end-tidal CO2 we
re measured at baseline and during graded reduction in arterial SpO(2)
to 85%, at normocapnia. Flow velocity and estimated cerebrovascular r
esistance (CVRe) were indexed and plotted against SpO(2). There was no
significant change in mean arterial pressure during desaturation to 8
5%, although the mean heart rate increased from 65 to 82 bpm. An incre
ase in MCA FVx and reciprocal decrease in CVRe were observed when SpO(
2) decreased to below 90%. These results suggest that hypoxemic cerebr
al vasodilatation may be measured noninvasively and that in normal hum
an volunteers, the threshold is at an SpO(2) of 90%, which is greater
than that previously reported. Implications: The ability to detect the
point at which cerebral blood vessels dilate using noninvasive techni
ques is clinically advantageous. We have attempted to do this using tr
anscranial Doppler sonography in volunteers whose inspired oxygen conc
entrations were gradually decreased. Thresholds of cerebral vasodilata
tion were found to be higher than those previously reported. These thr
esholds are important with regard to adequate perfusion in various pat
hologic states.