The brain is the exclusive or almost exclusive site of formation of 24S-hyd
roxycholesterol and we have shown that the circulating level of 24S-hydroxy
cholesterol is dependent upon the relation between cerebral production and
hepatic clearance. In the present work we determined plasma levels of 24S-h
ydroxycholesterol in patients with various neurological diseases. Eleven su
bjects with brain death occurring 6-10 h before collection of the plasma sa
mples had markedly reduced circulating levels of 24S-hydroxycholesterol (-4
3%, P < 0.001). Patients with advanced Alzheimer's disease and cerebral inf
lammatory diseases had slightly lower levels of 24S-hydroxycholesterol in p
lasma when compared to matched controls. Patients with acute ischemic strok
e, multiple sclerosis and primary brain tumors had levels not significantly
different from those of controls. The conditions leading to reduced plasma
levels of 24S-hydroxycholesterol had no significant effect on plasma level
s of another side-chain oxidized oxysterol, 27-hydroxycholesterol. Except f
or conditions characterized by very marked destruction of the central nervo
us system, different severe neurological diseases seem to have relatively s
mall effects on the flux of 24S-hydroxycholesterol from the brain, (C) 2000
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