Bempedoic Acid Lowers Low-Density Lipoprotein Cholesterol and Attenuates Atherosclerosis in Low-Density Lipoprotein Receptor-Deficient (LDLR+/- and LDLR-/-) Yucatan Miniature Pigs. 2018

Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
From the Robarts Research Institute (A.C.B., D.E.T., B.G.S., J.Y.E., C.G.S., J.G.P., M.W.H.).

Bempedoic acid (BemA; ETC-1002) is a novel drug that targets hepatic ATP-citrate lyase to reduce cholesterol biosynthesis. In phase 2 studies, BemA lowers elevated low-density lipoprotein cholesterol (LDL-C) in hypercholesterolemic patients. In the present study, we tested the ability of BemA to decrease plasma cholesterol and LDL-C and attenuate atherosclerosis in a large animal model of familial hypercholesterolemia. Gene targeting has been used to generate Yucatan miniature pigs heterozygous (LDLR+/-) or homozygous (LDLR-/-) for LDL receptor deficiency (ExeGen). LDLR+/- and LDLR-/- pigs were fed a high-fat, cholesterol-containing diet (34% kcal fat; 0.2% cholesterol) and orally administered placebo or BemA for 160 days. In LDLR+/- pigs, compared with placebo, BemA decreased plasma cholesterol and LDL-C up to 40% and 61%, respectively. In LDLR-/- pigs, in which plasma cholesterol and LDL-C were 5-fold higher than in LDLR+/- pigs, BemA decreased plasma cholesterol and LDL-C up to 27% and 29%, respectively. Plasma levels of triglycerides and high-density lipoprotein cholesterol, fasting glucose and insulin, and liver lipids were unaffected by treatment in either genotype. In the aorta of LDLR+/- pigs, BemA robustly attenuated en face raised lesion area (-58%) and left anterior descending coronary artery cross-sectional lesion area (-40%). In LDLR-/- pigs, in which lesions were substantially more advanced, BemA decreased aortic lesion area (-47%) and left anterior descending coronary artery lesion area (-48%). In a large animal model of LDLR deficiency and atherosclerosis, long-term treatment with BemA reduces LDL-C and attenuates the development of aortic and coronary atherosclerosis in both LDLR+/- and LDLR-/- miniature pigs.

UI MeSH Term Description Entries
D008078 Cholesterol, LDL Cholesterol which is contained in or bound to low density lipoproteins (LDL), including CHOLESTEROL ESTERS and free cholesterol. LDL Cholesterol,Cholesteryl Linoleate, LDL,LDL Cholesteryl Linoleate,Low Density Lipoprotein Cholesterol,beta-Lipoprotein Cholesterol,Cholesterol, beta-Lipoprotein,beta Lipoprotein Cholesterol
D008297 Male Males
D010641 Phenotype The outward appearance of the individual. It is the product of interactions between genes, and between the GENOTYPE and the environment. Phenotypes
D011973 Receptors, LDL Receptors on the plasma membrane of nonhepatic cells that specifically bind LDL. The receptors are localized in specialized regions called coated pits. Hypercholesteremia is caused by an allelic genetic defect of three types: 1, receptors do not bind to LDL; 2, there is reduced binding of LDL; and 3, there is normal binding but no internalization of LDL. In consequence, entry of cholesterol esters into the cell is impaired and the intracellular feedback by cholesterol on 3-hydroxy-3-methylglutaryl CoA reductase is lacking. LDL Receptors,Lipoprotein LDL Receptors,Receptors, Low Density Lipoprotein,LDL Receptor,LDL Receptors, Lipoprotein,Low Density Lipoprotein Receptor,Low Density Lipoprotein Receptors,Receptors, Lipoprotein, LDL,Receptor, LDL,Receptors, Lipoprotein LDL
D003324 Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. Arteriosclerosis, Coronary,Atherosclerosis, Coronary,Coronary Arteriosclerosis,Coronary Atherosclerosis,Left Main Coronary Artery Disease,Left Main Coronary Disease,Left Main Disease,Arterioscleroses, Coronary,Artery Disease, Coronary,Artery Diseases, Coronary,Atheroscleroses, Coronary,Coronary Arterioscleroses,Coronary Artery Diseases,Coronary Atheroscleroses,Left Main Diseases
D003998 Dicarboxylic Acids Acyclic acids that contain two carboxyl groups and have the formula HO2C-R-CO2H, where R may be an aromatic or aliphatic group. Acids, Dicarboxylic
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D005227 Fatty Acids Organic, monobasic acids derived from hydrocarbons by the equivalent of oxidation of a methyl group to an alcohol, aldehyde, and then acid. Fatty acids are saturated and unsaturated (FATTY ACIDS, UNSATURATED). (Grant & Hackh's Chemical Dictionary, 5th ed) Aliphatic Acid,Esterified Fatty Acid,Fatty Acid,Fatty Acids, Esterified,Fatty Acids, Saturated,Saturated Fatty Acid,Aliphatic Acids,Acid, Aliphatic,Acid, Esterified Fatty,Acid, Saturated Fatty,Esterified Fatty Acids,Fatty Acid, Esterified,Fatty Acid, Saturated,Saturated Fatty Acids
D005260 Female Females
D005786 Gene Expression Regulation Any of the processes by which nuclear, cytoplasmic, or intercellular factors influence the differential control (induction or repression) of gene action at the level of transcription or translation. Gene Action Regulation,Regulation of Gene Expression,Expression Regulation, Gene,Regulation, Gene Action,Regulation, Gene Expression

Related Publications

Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
January 2014, PloS one,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
June 2019, Molecular nutrition & food research,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
March 2012, The Yale journal of biology and medicine,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
April 2023, Journal of cardiovascular development and disease,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
August 2022, Journal of the American Heart Association,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
January 2015, PloS one,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
June 2018, Journal of cellular and molecular medicine,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
October 2018, Journal of cellular physiology,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
November 2005, Arteriosclerosis, thrombosis, and vascular biology,
Amy C Burke, and Dawn E Telford, and Brian G Sutherland, and Jane Y Edwards, and Cynthia G Sawyez, and P Hugh R Barrett, and Roger S Newton, and J Geoffrey Pickering, and Murray W Huff
May 2023, Atherosclerosis,
Copied contents to your clipboard!