Department of Clinical Pharmacology, University of Bonn, Bonn, Germany.
J Cardiovasc Pharmacol Ther. 2010 Dec;15(4):364-72. doi: 10.1177/1074248410371100. Epub 2010 Aug 6.
Lifibrol is a potent lipid-lowering drug with an unknown mechanism of action. We investigated its effects on lipoprotein and sterol metabolism in normocholesterolemic male participants. Seven participants were treated for 4 weeks with 600 mg/d lifibrol and 9 with 40 mg/d pravastatin in a double-blind randomized parallel-group trial. Kinetic studies were performed at baseline and under acute and chronic treatment. Turnover of apolipoprotein B-100 was investigated with endogenous stable-isotope labeling, and kinetic parameters were derived by multicompartmental modeling. Lathosterol and cholesterol metabolism were investigated using mass isotopomer distribution analysis (MIDA) after [1-(13)C]acetate labeling. Carbon metabolism was investigated by calculating the total isotope incorporation into newly formed sterols and measuring the disposal of acetate by (13)CO(2) breath analysis. Total- and low-density lipoprotein (LDL) cholesterol decreased by 18% and 27% under lifibrol and by 17% and 28% under pravastatin, respectively, whereas very-low-density lipoprotein (VLDL) cholesterol, triglycerides, and high-density lipoprotein (HDL) cholesterol did not change. Very-low-density lipoprotein apoB fractional synthesis and production increased under lifibrol but remained unchanged under pravastatin. Low-density lipoprotein apoB fractional synthesis and production increased under pravastatin but remained unchanged under lifibrol. Mass isotopomer distribution analysis indicated that both drugs decrease endogenous sterol synthesis after acute administration, but pravastatin had more powerful effects. Carbon-13 appearance in breath was higher during pravastatin than during lifibrol treatment. Mass isotopomer distribution analysis and carbon metabolism analysis indicated compartmentalization at the site of sterol synthesis, thus suggesting differential effects of the 2 drugs. Although having comparable lipid-lowering properties, lifibrol seems to have a mechanism of action distinct from that of statins. Lifibrol could serve as a model compound for the development of new lipid-lowering agents.
利伐布洛尔是一种强效降脂药物,其作用机制尚不清楚。我们研究了它对正常胆固醇男性参与者脂蛋白和固醇代谢的影响。在一项双盲随机平行组试验中,7 名参与者接受 600 毫克/天利伐布洛尔治疗 4 周,9 名参与者接受 40 毫克/天普伐他汀治疗。在基线和急性及慢性治疗下进行了动力学研究。采用内源性稳定同位素标记研究载脂蛋白 B-100 的周转,通过多房室模型进行动力学参数推导。用质量同位素分布分析(MIDA)研究[1-(13)C]乙酸盐标记后的羊毛甾醇和胆固醇代谢。通过计算新形成固醇中总同位素掺入量和测量(13)CO2 呼气分析中乙酸盐的处置来研究碳代谢。总胆固醇和低密度脂蛋白(LDL)胆固醇分别下降 18%和 27%,而极低密度脂蛋白(VLDL)胆固醇、甘油三酯和高密度脂蛋白(HDL)胆固醇没有变化。利伐布洛尔使 VLDL apoB 分数合成和产生增加,而普伐他汀则没有变化。普伐他汀使 LDL apoB 分数合成和产生增加,而利伐布洛尔则没有变化。质量同位素分布分析表明,两种药物在急性给药后均降低内源性固醇合成,但普伐他汀的作用更强。碳-13 在呼吸中的出现率在普伐他汀治疗期间高于利伐布洛尔治疗期间。质量同位素分布分析和碳代谢分析表明,固醇合成部位的分隔,因此提示两种药物的作用存在差异。尽管利伐布洛尔具有类似的降脂特性,但它的作用机制似乎与他汀类药物不同。利伐布洛尔可作为开发新型降脂药物的模型化合物。