Malmendier C L, Delcroix C
Atherosclerosis. 1985 May;55(2):161-9. doi: 10.1016/0021-9150(85)90095-4.
This study investigates the influence of pharmacological doses of fenofibrate on HDL and LDL metabolism in 5 familial hypercholesterolemia heterozygotes. Fenofibrate lowered plasma low density lipoprotein cholesterol (20%, P less than 0.025), triglycerides (37%: P less than 0.005) and apolipoprotein B (14%: P less than 0.05) but increased apo A-I (20%; P = 0.01). Kinetic studies showed that the drug markedly increased the fractional catabolic rate of LDL-apo B by 59% and its synthetic rate by 36%. Fractional catabolic rate of apo A-I was also increased by 26% but accompanied by a much greater increase of its synthetic rate (49%). Thus the change in balance between catabolism and synthesis of both apoproteins affected by fenofibrate accounts for the observed plasma concentration changes, which may be considered as favourable with regard to the management of atherosclerosis.
本研究调查了药理剂量的非诺贝特对5名家族性高胆固醇血症杂合子高密度脂蛋白(HDL)和低密度脂蛋白(LDL)代谢的影响。非诺贝特降低了血浆低密度脂蛋白胆固醇(20%,P<0.025)、甘油三酯(37%:P<0.005)和载脂蛋白B(14%:P<0.05),但增加了载脂蛋白A-I(20%;P=0.01)。动力学研究表明,该药物显著提高了LDL-载脂蛋白B的分解代谢率59%,其合成率提高了36%。载脂蛋白A-I的分解代谢率也提高了26%,但其合成率的增加幅度更大(49%)。因此,非诺贝特影响的两种载脂蛋白分解代谢与合成之间平衡的变化解释了观察到的血浆浓度变化,就动脉粥样硬化的管理而言,这些变化可能被认为是有利的。