Wang C S, McConathy W J, Kloer H U, Alaupovic P
J Clin Invest. 1985 Feb;75(2):384-90. doi: 10.1172/JCI111711.
From a total of 22 hypertriglyceridemic subjects tested, 14 subjects were selected on the basis of normal postheparin plasma lipoprotein lipase (LPL) levels and the presence of LPL inhibitory activity in their fasting plasma. The inhibitory activity was detected in both the lipoprotein fraction (d less than 1.25 g/ml) and the lipoprotein-deficient fraction (d greater than 1.25 g/ml). Correlational analyses of LPL inhibitory activity and apolipoprotein levels present in the lipoprotein fraction (d less than 1.25 g/ml) indicated that only apolipoprotein C-III (ApoC-III) was significantly correlated (r = 0.602, P less than 0.05) with the inhibition activity of the lipoprotein fraction. Furthermore, it was found that LPL-inhibitory activities of the plasma lipoprotein fraction and lipoprotein-deficient fraction were also correlated (r = 0.745, P less than 0.005), though the activity in the lipoprotein-deficient plasma was not related to the ApoC-III or apolipoprotein E levels. Additional correlational analyses indicated that the LPL levels in the postheparin plasma of these subjects were inversely related to the levels of plasma apolipoproteins C-II, C-III, and E. To explain some of these observations, we directly examined the in vitro effect of ApoC-III on LPL activity. The addition of ApoC-III-2 resulted in a decreased rate of lipolysis of human very low density lipoproteins by LPL. Kinetic analyses indicated that ApoC-III-2 was a noncompetitive inhibitor of LPL suggesting a direct interaction of the inhibitor with LPL. Results of these studies suggest that ApoC-III may represent a physiologic modulator of LPL activity levels and that the incidence of LPL inhibitory activity in the plasma of hypertriglyceridemic subjects is more common than previously recognized.
在总共22名接受测试的高甘油三酯血症受试者中,根据肝素后血浆脂蛋白脂肪酶(LPL)水平正常以及其空腹血浆中存在LPL抑制活性,选择了14名受试者。在脂蛋白部分(d小于1.25 g/ml)和脂蛋白缺乏部分(d大于1.25 g/ml)均检测到抑制活性。对脂蛋白部分(d小于1.25 g/ml)中存在的LPL抑制活性和载脂蛋白水平进行的相关性分析表明,只有载脂蛋白C-III(ApoC-III)与脂蛋白部分的抑制活性显著相关(r = 0.602,P小于0.05)。此外,发现血浆脂蛋白部分和脂蛋白缺乏部分的LPL抑制活性也相关(r = 0.745,P小于0.005),尽管脂蛋白缺乏血浆中的活性与ApoC-III或载脂蛋白E水平无关。进一步的相关性分析表明,这些受试者肝素后血浆中的LPL水平与血浆载脂蛋白C-II、C-III和E的水平呈负相关。为了解释其中一些观察结果,我们直接检测了ApoC-III对LPL活性的体外作用。添加ApoC-III-2导致LPL对人极低密度脂蛋白的脂解速率降低。动力学分析表明,ApoC-III-2是LPL的非竞争性抑制剂,表明抑制剂与LPL直接相互作用。这些研究结果表明,ApoC-III可能是LPL活性水平的生理调节剂,并且高甘油三酯血症受试者血浆中LPL抑制活性的发生率比以前认识到的更为常见。