Dachet C, Jacotot B, Buxtorf J C
Atherosclerosis. 1985 Dec;58(1-3):261-8. doi: 10.1016/0021-9150(85)90071-1.
In this study Probucol transport and the effect of the drug on lipoprotein composition in 9 cases of type IIa hypercholesterolemia were investigated. Probucol lowered plasma cholesterol by 20%, without affecting triglycerides. HDL cholesterol was decreased and a slight reduction in LDL cholesterol was noted. This was due to a reduction in the number of circulating lipoprotein particles, without modification in the lipid/protein ratio, mainly cholesterol/protein ratio. Probucol was almost entirely removed by lipoproteins; 75% of the drug was found in LDL, the remainder being equally distributed in VLDL and HDL. There was no correlation between the serum Probucol level, or the amount of Probucol bound to lipoproteins, and the decrease in serum or lipoprotein cholesterol. However, there was a significant increase of the EC/TC (esterified cholesterol/total cholesterol) ratio in VLDL and LDL, but not in HDL.
本研究调查了9例IIa型高胆固醇血症患者中普罗布考的转运情况以及该药物对脂蛋白组成的影响。普罗布考使血浆胆固醇降低了20%,而对甘油三酯无影响。高密度脂蛋白胆固醇降低,低密度脂蛋白胆固醇略有降低。这是由于循环脂蛋白颗粒数量减少,脂质/蛋白质比例,主要是胆固醇/蛋白质比例未改变。普罗布考几乎完全被脂蛋白清除;75%的药物存在于低密度脂蛋白中,其余药物在极低密度脂蛋白和高密度脂蛋白中平均分布。血清普罗布考水平或与脂蛋白结合的普罗布考量与血清或脂蛋白胆固醇的降低之间无相关性。然而,极低密度脂蛋白和低密度脂蛋白中的酯化胆固醇/总胆固醇(EC/TC)比值显著升高,而高密度脂蛋白中则未升高。