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普罗布考对血浆脂蛋白亚组分及脂蛋白脂肪酶和肝甘油三酯脂肪酶活性的影响。

Effects of probucol on plasma lipoprotein subfractions and activities of lipoprotein lipase and hepatic triglyceride lipase.

作者信息

Homma Y, Moriguchi E H, Sakane H, Ozawa H, Nakamura H, Goto Y

机构信息

Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan.

出版信息

Atherosclerosis. 1991 Jun;88(2-3):175-81. doi: 10.1016/0021-9150(91)90079-i.

Abstract

The effects of 12 weeks treatment with probucol on plasma lipoprotein subfraction levels and on LPL and HTGL activities were investigated. Plasma VLDL-C, VLDL-TG, VLDL-apo B levels were not changed. Probucol significantly reduced plasma IDL-C and IDL-apo B levels by 26.7% and 23.8%, respectively. Plasma cholesterol and apo B levels of large light LDL (LDL1) were decreased significantly by 27.8% and 23.2% by probucol treatment. Plasma cholesterol and apo B levels of small heavy LDL (LDL2) remained unchanged. Probucol markedly reduced plasma HDL2 levels. The reduction rates of plasma TC, TG and apo A-I levels of HDL2 were 43.0%, 43.6% and 47.0%. Probucol significantly decreased HDL3-C and HDL3-apo A-I levels by 18.0% and 19.2%. LPL activities in the post-heparin plasma were decreased significantly from 2.53 +/- 0.71 mumol free fatty acids (FFA)/ml/h to 1.71 +/- 0.71 mumol FFA/ml/h by probucol while HTGL activities remained unchanged. We conclude that probucol suppresses LPL activity and decreases plasma IDL, LDL1 and HDL2 levels due to disturbances of VLDL conversion to LDL1 via IDL and of HDL3 conversion to HDL2.

摘要

研究了普罗布考治疗12周对血浆脂蛋白亚组分水平以及脂蛋白脂肪酶(LPL)和肝甘油三酯脂肪酶(HTGL)活性的影响。血浆极低密度脂蛋白胆固醇(VLDL-C)、极低密度脂蛋白甘油三酯(VLDL-TG)、极低密度脂蛋白载脂蛋白B(VLDL-apo B)水平未发生变化。普罗布考分别使血浆中间密度脂蛋白胆固醇(IDL-C)和中间密度脂蛋白载脂蛋白B(IDL-apo B)水平显著降低了26.7%和23.8%。普罗布考治疗使大而轻的低密度脂蛋白(LDL1)的血浆胆固醇和载脂蛋白B水平显著降低,降幅分别为27.8%和23.2%。小而密的低密度脂蛋白(LDL2)的血浆胆固醇和载脂蛋白B水平保持不变。普罗布考显著降低了血浆高密度脂蛋白2(HDL2)水平。HDL2的血浆总胆固醇(TC)、甘油三酯(TG)和载脂蛋白A-I(apo A-I)水平的降低率分别为43.0%、43.6%和47.0%。普罗布考使高密度脂蛋白3胆固醇(HDL3-C)和高密度脂蛋白3载脂蛋白A-I(HDL3-apo A-I)水平显著降低,降幅分别为18.0%和19.2%。普罗布考使肝素后血浆中的LPL活性从2.53±0.71微摩尔游离脂肪酸(FFA)/毫升/小时显著降至1.71±0.71微摩尔FFA/毫升/小时,而HTGL活性保持不变。我们得出结论,普罗布考通过干扰极低密度脂蛋白经中间密度脂蛋白转化为低密度脂蛋白1以及高密度脂蛋白3转化为高密度脂蛋白2,抑制LPL活性并降低血浆IDL、LDL1和HDL2水平。

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