
pmid: 2324647
Plasma lipids and apolipoproteins, and hepatic LDL receptor and HMG-CoA reductase activities in biopsy samples were measured in high- and low-responding rhesus monkeys maintained on a cholesterol-rich and regular diets. The effect of a 30-day cholestyramine treatment on the above parameters under both dietary conditions was also determined. On the cholesterol-rich diet the high-responders, when compared to the low-responders, had several-fold increased plasma cholesterol and apoB concentrations and significantly lower HDL apoA-I and cholesterol concentrations. Hepatic LDL receptor and HMG-CoA reductase activities were not detectable in the high-responders, while the low-responders expressed a reduced number of LDL receptors of normal affinity. Administration of cholestyramine resulted in a rapid induction of the hepatic LDL receptors in the high-responders and a small additional increase in the low-responders. Cholestyramine treatment also stimulated the expression of the hepatic HMG-CoA reductase in both groups of monkeys. These changes were accompanied by a dramatic drop in plasma cholesterol and apoB concentrations in the high-responders and, to a lesser extent, in the low-responders. Plasma HDL concentrations in the high-responders rose to levels higher than those seen in the low-responders. The affinity and receptor number were similar in both groups of monkeys on the control diet, but the low-responders had significantly higher HMG-CoA reductase activities. Administration of cholestyramine during the control diet had a small but significant additional effect on the hepatic LDL receptors of the low-responders but not of the high-responders.(ABSTRACT TRUNCATED AT 250 WORDS)
Male, Cholestyramine Resin, QD415-436, Lipid Metabolism, Biochemistry, Lipids, Macaca mulatta, Cholesterol, Dietary, Apolipoproteins, Intestinal Absorption, Liver, Receptors, LDL, Animals, Hydroxymethylglutaryl CoA Reductases
Male, Cholestyramine Resin, QD415-436, Lipid Metabolism, Biochemistry, Lipids, Macaca mulatta, Cholesterol, Dietary, Apolipoproteins, Intestinal Absorption, Liver, Receptors, LDL, Animals, Hydroxymethylglutaryl CoA Reductases
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