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Journal of Lipid Research, Vol 25, 780-790, Copyright © 1984 by Lipid Research, Inc.
YA Kesaniemi and SM Grundy
The mechanisms for the hypocholesterolemic action of probucol were examined
in 17 patients with various levels of plasma cholesterol and triglycerides
(TG). All the patients were studied on a metabolic ward. The first period
of 6 weeks was for control. Thereafter, probucol was started, and after 2-6
months of drug treatment, the patients were readmitted for another 6-week
period for a repeat study. During treatment with probucol, the cholesterol
decreased in total plasma by an average of 12%, in low density lipoproteins
(LDL) by 11%, and in high density lipoproteins (HDL) by 9%. The TG in total
plasma and in very low density lipoproteins (VLDL) remained unchanged
during probucol treatment. Turnover of low density lipoprotein apoprotein
(apoLDL) was estimated following injection of 125I-labeled apoLDL. Probucol
increased the fractional catabolic rate (FCR) for apoLDL by an average of
23%, but did not change apoLDL synthesis. The drug produced no consistent
changes in fecal excretion of cholesterol (neutral steroids) and bile
acids, in cholesterol absorption, in lipid composition of gallbladder bile,
in biliary secretion of cholesterol and bile acids, or in the activities of
lipoprotein lipase and hepatic lipase. These data show that probucol lowers
LDL by increasing its catabolism. This effect appears to be independent of
any changes in metabolism of cholesterol or bile acids.
ARTICLES
Influence of probucol on cholesterol and lipoprotein metabolism in man
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