Key result
Cholestyramine rapidly upregulates hepatic LDL receptors and sharply lowers plasma cholesterol and apoB levels.
Why the study?
The relationship between hepatic LDL receptor and HMG-CoA reductase activities and plasma lipids in high- and low-responding rhesus monkeys under different diets and cholestyramine treatment was unclear.
Answers are grounded in this paper and cite their sources.
May support cholestyramine's LDL-lowering mechanism via receptor induction; extends primate mechanistic data but leaves open human translation.
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)
No takes yet. Share an insight, caveat, or question.
Dory et al. (1990) studied High- and low-responding rhesus monkeys. Cholestyramine vs. Baseline / Regular diet was evaluated on Plasma lipids, apolipoproteins, hepatic LDL receptor, and HMG-CoA reductase activities. A 30-day cholestyramine treatment rapidly induced hepatic LDL receptors and stimulated HMG-CoA reductase expression, accompanied by a dramatic drop in plasma cholesterol and apoB concentrations.
Synapse has enriched 10 related papers. Consider them for comparative context: