Heterozygous Ldlr-Deficient Hamster as a Model to Evaluate the Efficacy of PCSK9 Antibody in Hyperlipidemia and Atherosclerosis

• Published in: International journal of molecular sciences Vol. 20; no. 23; p. 5936
• Main Authors: Wu, Yue, Xu, Ming-Jiang, Cao, Zhiyou, Yang, Chun, Wang, Jinjie, Wang, Bijue, Liu, Jian, Wang, Yuhui, Xian, Xunde, Zhang, Fang, Liu, George, Chen, Xiaoli
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 26.11.2019; MDPI
• Subjects: Abdomen; Animal models; Animals; Antibodies; Antibodies, Monoclonal, Humanized - administration & dosage; Antibodies, Monoclonal, Humanized - pharmacology; Aorta; Arteriosclerosis; Atherogenesis; Atherosclerosis; Atherosclerosis - chemically induced; Atherosclerosis - drug therapy; Atherosclerosis - genetics; Cardiovascular disease; Cholesterol; Cholesterol, LDL - blood; Cholesteryl ester transfer protein; Coronary vessels; Correlation analysis; Cricetinae; Diet, High-Fat - adverse effects; Disease Models, Animal; Drug development; Dyslipidemia; Ezetimibe - administration & dosage; Ezetimibe - pharmacology; Hamsters; Heterozygote; High cholesterol diet; High fat diet; Homeostasis; Humans; Hyperlipidemia; Hyperlipidemias - chemically induced; Hyperlipidemias - drug therapy; Hyperlipidemias - genetics; Kexin; Lipids; Lipoproteins; Low density lipoprotein; Low density lipoprotein receptors; Male; Metabolic disorders; Metabolism; Mutation; Plasma; Plasma levels; Proprotein Convertase 9 - antagonists & inhibitors; Proprotein convertases; Proteins; Receptor density; Receptors, LDL - deficiency; Subtilisin; Treatment Outcome; Triglycerides; atherosclerosis; proprotein convertase subtilisin/kexin type 9; low-density lipoprotein receptor; animal model; dyslipidemia; low-density lipoprotein
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms20235936

Proprotein convertase subtilisin/kexin type 9 (PCSK9) plays a key role in cholesterol homeostasis and atherogenesis. However, there are only limited rodent models, with a functional low-density lipoprotein receptor (LDLR) pathway and cholesteryl ester transfer protein (CETP) to evaluate the drug candidates targeting the PCSK9/LDLR pathway, that are translatable to humans. Here, by using our recently generated LDLR heterozygote ( ) hamster model with functional LDLR pathway and CETP function, we seek to evaluate the effect of a PCSK9 antibody, evolocumab, on dyslipidemia and atherosclerosis compared with ezetimibe, an effective inhibitor of cholesterol absorption, as a positive therapeutic control. We show that the plasma levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), and triglyceride (TG) were significantly increased in hamsters fed a high-fat high-cholesterol (HFHC) diet; therefore, areas of atherosclerotic lesion in the aorta were obviously increased and positively correlated with plasma LDL-C and TC. Circulating free PCSK9 was downregulated by the HFHC diet and was undetectable in the evolocumab treated group, as expected. Most importantly, either evolocumab or ezetimibe treatment prevented HFHC diet-induced hyperlipidemia and subsequent atherosclerotic plaque formation. The results indicate that +/- hamsters fed an HFHC diet represent an ideal rodent model to evaluate drug candidates that affect LDLR pathways.