作者: Thomas M.A. Bocan , Michelle J. Mazur , Sandra Bak Mueller , Edie Quenby Brown , D.Robert Sliskovic
DOI: 10.1016/0021-9150(94)90198-8
关键词: Simvastatin 、 Reductase 、 Lesion 、 Internal medicine 、 Pravastatin 、 Atorvastatin 、 Biology 、 Endocrinology 、 Cholesterol 、 HMG-CoA reductase 、 Lovastatin 、 Cardiology and Cardiovascular Medicine
摘要: Atherosclerotic lesion development was assessed in the thoracic aorta and chronically denuded iliac-femoral artery of hypercholesterolemic New Zealand White rabbits using inhibitors 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase which have previously been shown to possess varying degrees hepatoselectivity rats. Atorvastatin, known as CI-981 (2.5 mg/kg), PD135022 (1.0 simvastatin lovastatin PD134965 pravastatin mg/kg) BMY22089 were added a 0.5% cholesterol, 3% peanut, coconut oil diet fed for 8 weeks. Although reductions plasma total cholesterol 27% 60%, VLDL-cholesterol 31% 71% exposure 37% 43% obtained, no correlation between these parameters vascular lipid content, size or monocyte-macrophage content noted. Iliac-femoral unchanged; however, atorvastatin significantly reduced by 45%-62%. Atorvastatin 67% 72%. Simvastatin, decreased content; unchanged. Pravastatin had effect on content. No compound extent aortic lesions. We concluded that changes lipids lipoproteins noted with various HMG-CoA did not account beneficial atherosclerotic development. The antiatherosclerotic potential compound-specific clearly class effect.