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Inverse relationship between LDL cholesterol and PCSK9 plasma levels in dyslipidemic cynomolgus monkeys: Effects of LDL lowering by ezetimibe in the absence of statins
Authors:Hannes Hentze  Kristian K. Jensen  Ser Mien Chia  Douglas G. Johns  Rachel J. Shaw  Harry R. Davis Jr.  Shian-Jiun Shih  Kenny K. Wong
Affiliation:1. Translational Medicine Research Centre (TMRC) Singapore, MSD, 8 Biomedical Grove, Neuros Buidling, Singapore 138665, Singapore;2. Department of Atherosclerosis, Merck Research Laboratories, 126 E. Lincoln Avenue, PO Box 2000, Rahway, NJ 07065-0900, USA
Abstract:

Objectives

To assess the lipid-lowering efficacy of ezetimibe in dyslipidemic cynomolgus monkeys comparing two dosing methods, and to evaluate PCSK9 plasma levels during dyslipidemia induction by feeding a high-fat/high-cholesterol diet (HFD), ezetimibe (Zetia®, Ezetrol®) treatment, ezetimibe washout, and HFD washout.

Methods and results

Twenty dyslipidemic cynomolgus monkeys on HFD for seven months (LDL cholesterol 100–400 mg/dL) were randomized into two groups and treated with ezetimibe for two weeks, either by oral gavage or by using food treats. The lipid-lowering effects of ezetimibe were identical between the two groups. After treatment, mean LDL cholesterol was decreased by 58% (174–72 mg/dL), total cholesterol by 42% (241–138 mg/dL), and PCSK9 levels were increased by 137% (147–314 ng/mL). PCSK9 levels on regular diet before and after HFD were also inversely correlated to LDL cholesterol.

Conclusions

In a cynomolgus dyslipidemia model, PCSK9 levels are inversely correlated with LDL cholesterol in the absence of statin treatment, regardless whether lipid changes are modulated by diet or ezetimibe treatment.
Keywords:Non-human primate   Dyslipidemia   Ezetimibe   PCSK9
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