Adameová A, Kuzelová M, Faberová V, Svec P
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University, Bratislava, Slovak Republic.
Pharmazie. 2005 Sep;60(9):714-5.
The use of inhibitors of enzyme acyl-CoA: cholesterol acyltransferase (ACAT) seems to be a novel potential approach for a therapeutic treatment of dyslipidaemias and atherosclerosis. VULM 1457 is an ACAT inhibitor, which has expressed potent hypolipidemic and antiatherosclerotic effects in previous studies. In this study, we used streptozocin-induced diabetic rats, which were fed a fat-cholesterol diet to evaluate the affect of VULM 1457 on the atherogenic lipids levels in both plasma and liver. VULM 1457, with a slight influence on triglyceride levels, significantly reduced plasma and hepatic cholesterol concentrations (p < 0.05, p < 0.001; respectively) in the diabetic-hypercholesterolaemic rats.
使用酶酰基辅酶A:胆固醇酰基转移酶(ACAT)抑制剂似乎是治疗血脂异常和动脉粥样硬化的一种新型潜在方法。VULM 1457是一种ACAT抑制剂,在先前的研究中已表现出强大的降血脂和抗动脉粥样硬化作用。在本研究中,我们使用链脲佐菌素诱导的糖尿病大鼠,给它们喂食高脂高胆固醇饮食,以评估VULM 1457对血浆和肝脏中致动脉粥样硬化脂质水平的影响。VULM 1457对甘油三酯水平影响轻微,但显著降低了糖尿病高胆固醇血症大鼠的血浆和肝脏胆固醇浓度(分别为p < 0.05,p < 0.001)。