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Journal of Lipid Research, Vol 26, 1230-1240, Copyright © 1985 by Lipid Research, Inc.
SJ Robins, JM Fasulo, MA Collins and GM Patton
The turnover of plasma cholesterol and de novo cholesterol synthesis were
measured simultaneously in the live rat, immediately after administration
of [3H]water together with a large volume exchange transfusion of whole
blood prelabeled with [14C]cholesterol. It was possible to separate the
exchange of unesterified cholesterol from the uptake and secretion of
lipoprotein cholesteryl ester, and also to assess the impact of plasma
cholesterol exchange on the measurement of in vivo rates of
cholesterolgenesis by individual tissues. Cholesterol was measured by an
HPLC procedure that effectively separated cholesterol from other
structurally similar sterols, and synthesis was determined by the
incorporation of [3H]water into cholesterol. Plasma unesterified
cholesterol turnover was multiphasic and exceedingly rapid (initial T1/2,
4.1 min) in contrast to the near linear and much slower turnover of plasma
cholesteryl ester (initial T1/2, 59.4 min). Plasma unesterified cholesterol
equilibrated with different tissues at different rates, with the liver and
adrenal equilibrating most rapidly. Full equilibration of plasma
unesterified cholesterol was not achieved with any tissue during the course
of this study. For rapidly exchanging tissues like the liver, which was
responsible for about 60% of plasma unesterified cholesterol exchange,
unesterified cholesterol appeared to be kinetically compartmentalized into
rapidly, and much less rapidly, exchangeable pools. After [3H]water
administration, the content of newly synthesized cholesterol was greatest
in the liver, adrenal, and intestine, and appreciably lower in all other
tissues studied. Hepatectomy and intestinal resection resulted in a
profound reduction of newly synthesized cholesterol in the plasma and
adrenal, but no certain change in the already low amounts at other sites.
Thus, while it is clear that appreciable amounts of newly synthesized
cholesterol in the adrenal were derived from the plasma by exchange, it was
not possible to make this assessment for other selected individual tissues.
When, however, newly synthesized cholesterol was determined in the total
mass of all extrahepatic and extraintestinal tissues together, exchange
could be calculated to account for close to 50% of the new cholesterol
recovered in the carcass (in studies of 60 min duration). After correcting
for exchange, the liver accounted for 82% of all newly synthesized
cholesterol, the intestine for about 10%, and the remaining tissues of the
body for just 9%. These results are in marked contrast to recent findings
of others and demonstrate that in the live rat cholesterol synthesis is
principally confined to the liver.
ARTICLES
Cholesterol exchange and synthesis in the live rat
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