G. Cai et Tp. Carr, Biliary cholesterol and bile acid excretion do not increase in hamsters fed cereal-based diets containing cholesterol, METABOLISM, 48(3), 1999, pp. 400-405
The major compensatory responses to increased cholesterol consumption are d
ecreased cholesterol synthesis and increased cholesterol excretion through
the bile either as free cholesterol or bile acids. The objective of this st
udy was to test the hypothesis that biliary cholesterol excretion is increa
sed in hamsters fed low levels of cholesterol reflecting normal human intak
e. The hypothesis was based on observations that hamsters generally resist
changes in bile acid synthesis when fed large amounts of cholesterol: there
fore, increased biliary cholesterol excretion represents a potentially sign
ificant pathway for elimination of excess cholesterol in this species, Hams
ters were fed modified NIH-07 cereal-based diets containing 0.02%, 0.03%, a
nd 0.05% cholesterol (0.04, 0.06, and 0.10 mp cholesterol/kcal, respectivel
y). The primary response to increasing amounts of dietary cholesterol was d
ownregulation of whole-body cholesterol synthesis, reduced from 3.93 +/- 0.
14 mu mol . d(-1) . 100 g(-1) body weight in hamsters fed 0.02% cholesterol
to 0.52 +/- 0.14 mu mol . d(-1) . 100 g(-1) in the 0.05% cholesterol group
. Biliary cholesterol excretion was also slightly reduced in hamsters fed 0
.05% cholesterol, whereas bile acid excretion was not altered by dietary ch
olesterol, Despite a pronounced downregulation of whole-body cholesterol sy
nthesis, liver and plasma cholesterol concentrations increased in hamsters
fed 0.05% cholesterol, The data indicate that increased biliary cholesterol
excretion is not: a major compensatory route of cholesterol excretion in h
amsters consuming cholesterol, Furthermore, cholesterol added to the diet a
t: 0.05% appears to be the approximate threshold at which compensatory mech
anisms can prevent increases in liver and plasma cholesterol in male Syrian
hamsters, Consequently, this species may be an appropriate animal model fo
r "hyperresponding" individuals in the human population. Copyright (C) 1999
by W.B. Saunders Company.