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Journal of Lipid Research, Vol 24, 1321-1328, Copyright © 1983 by Lipid Research, Inc.
CR Pullinger and GF Gibbons
The true rate of sterol synthesis in liver cells was determined by
measurement of the weight of desmosterol produced over a given time period
during incubations in the presence of triparanol. The simultaneous presence
of tritiated water (3H2O) during the incubations permitted a direct
observation of the weight of tritium incorporated into a given mass of
newly synthesized sterol. The incorporation of tritium per atom of sterol
carbon (H/C ratio) was lower than some previously reported values and
suggests that a sizeable proportion of the reducing equivalents (NADPH)
required for sterol synthesis arises via the pentose phosphate pathway. The
H/C ratio changed significantly with length of the incubation period. The
value of the ratio was also dependent upon whether the acetyl-CoA units
utilized for sterol synthesis were derived predominantly from a
carbohydrate or a fatty acid source.
ARTICLES
The relationship between the rate of hepatic sterol synthesis and the incorporation of [3H]water
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