Formation of oxysterols from different pools of cholesterol as studied by stable isotope technique: cerebral origin of most circulating 24S-hydroxycholesterol in rats, but not in mice
S. Meaney et al., Formation of oxysterols from different pools of cholesterol as studied by stable isotope technique: cerebral origin of most circulating 24S-hydroxycholesterol in rats, but not in mice, BBA-MOL C B, 1486(2-3), 2000, pp. 293-298
Citations number
13
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
In order to study the origin of different oxysterols in the circulation, in
particular 24S-hydroxycholesterol, different pools of cholesterol in rat a
nd mouse were labelled by feeding the animals with a diet supplemented with
0.3 or 0.5% hexadeuterium-labelled cholesterol, respectively, for 10 days.
The incorporation of deuterium label in cholesterol and different oxystero
ls was measured by combined gas chromatography-mass spectrometry in selecte
d tissues and in the circulation. In both rat and mouse, a high incorporati
on of label was found in cholesterol present in serum and liver (up to 77%)
. Incorporation of label was similar in 7 alpha- and 7 beta-hydroxycholeste
rol of the same origin. There was no significant incorporation of deuterium
in brain cholesterol, and little or no incorporation in the brain oxystero
ls investigated, in both animals. In the testis, the incorporation of the d
euterium label in cholesterol was less than half of that in the liver, with
similarly reduced labelling of the testicular oxysterols. 24S-Hydroxychole
sterol in the circulation contained a deuterium content that was about 50%
of that of serum and liver cholesterol in the mouse experiment and about 30
% in the rat experiment. Thus, about 50% of circulating 24S-hydroxycholeste
rol in the mouse and about 70% of this fraction in the rat must originate f
rom pools of cholesterol that are not in equilibrium with plasma and liver
cholesterol. The liver is probably responsible for a considerable part of t
he extracerebral formation of 24S-hydroxycholesterol, since this organ cont
ained detectable amounts of 24S-hydroxycholesterol with a relatively high i
ncorporation of deuterium in both animal species. The results are consisten
t with a cerebral origin of more than half of the 24S-hydroxycholesterol in
the circulation of rats, but not in mice. (C) 2000 Elsevier Science B.V. A
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