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Journal of Lipid Research, Vol 35, 1878-1887, Copyright © 1994 by Lipid Research, Inc.
G Salen, AK Batta, GS Tint, S Shefer and GC Ness
We investigated the relationship between plasma cholestanol (5 alpha-
dihydrocholesterol) concentrations and the activity and mRNA levels of
cholesterol 7 alpha-hydroxylase, the rate-controlling enzyme for bile acid
synthesis, in three female sitosterolemic homozygotes. In this lipid
storage disease, large amounts of plant sterols and cholestanol accumulate
because of hyperabsorption and endogenous synthesis, respectively. Plasma
cholestanol concentrations were 14 times greater in the three
sitosterolemic homozygotes than the mean for five control subjects. To
investigate the cholestanol biosynthetic pathway, tracer doses of two
putative precursors, [1,2-3H]4-cholesten-3-one and [4- 14C]7
alpha-hydroxycholesterol were injected intravenously into a homozygote, and
radioactivity was sought in cholestanol, bile acids, cholesterol, and
sitosterol fractions isolated from plasma and bile. Tritium was
concentrated only in cholestanol; neither cholesterol, sitosterol nor bile
acids were derived from [1,2-3H]4-cholesten-3-one. In contrast, bile acids
were labeled exclusively with 14C from [4-14C]7 alpha-hydroxycholesterol;
no 14C radioactivity was detected in cholestanol. Mathematical analysis of
specific activity versus time curves for [3H]cholestanol revealed very slow
decay, large exchangeable pools, and enhanced synthesis in the
sitosterolemic homozygote. Measurements of cholesterol 7 alpha-hydroxylase
activity were 39% lower in whole liver microsomes from three sitosterolemic
homozygotes that contained 19% plant sterols as compared to the mean value
for six control microsomal specimens that contained 0.1% plant sterols.
Removal of the excess plant sterols from the microsomes, in vitro,
normalized microsomal cholesterol 7 alpha-hydroxylase activity in the
homozygotes but did not affect enzyme activity in the controls. Equal
amounts of cholesterol 7 alpha-hydroxylase mRNA were detected in the livers
of both control and sitosterolemic subjects. Bile acid malabsorption after
ileal bypass surgery stimulated cholesterol 7 alpha-hydroxylase activity
78% in sitosterolemic whole liver microsomes and reduced plasma
cholesterol, sitosterol, and cholestanol levels 61%, 55% and 91%,
respectively, producing a pronounced decrease in the
cholestanol/cholesterol ratio without changing the sitosterol/cholesterol
ratio. These results demonstrate that increased cholestanol is synthesized
from 4-cholesten-3-one and not 7 alpha- hydroxycholesterol in
sitosterolemia. Enhanced pools and plasma concentrations are related
inversely to hepatic cholesterol 7 alpha- hydroxylase activity. Competitive
inhibition of cholesterol 7 alpha- hydroxylase by the large microsomal
plant sterol pool diverts cholesterol into cholestanol. Alternatively,
stimulating cholesterol 7 alpha-hydroxylase activity after ileal bypass
surgery markedly diminished plasma cholestanol levels.(ABSTRACT TRUNCATED
AT 400 WORDS)
ARTICLES
Inverse relationship between plasma cholestanol concentrations and bile acid synthesis in sitosterolemia
VA Medical Center, East Orange, NJ 07018.
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