Greten H, DeGrella R, Klose G, Rascher W, de Gennes J L, Gjone E
J Lipid Res. 1976 May;17(3):203-10.
Postheparin plasma lipolytic activity consists of two hydrolytic activities, hepatic triglyceride lipase and lipoprotein lipase. These two enzymes were separated and partially purified by means of ammonium sulfate precipitation and affinity chromatography using Sepharose with covalently linked heparin and concanavalin A, respectively. Antibodies were produced against hepatic triglyceride lipase and they did not cross react with lipoprotein lipase. Optimal conditions for selective precipitation of hepatic lipase and specific measurement of these two lipases were investigated. This method was applied to the study of 15 patients with hypertriglyceridemia and 8 patients with familial lecithin-cholesterol-acyltransferase deficiency of whom 6 also had a marked elevated plasma triglyceride concentration. All patients had normal values of hepatic plasma lipase. All 8 patients with Type I and 2 of 4 patients with Type V hyperlipoproteinemia had lipoprotein lipase activities that were markedly reduced. The patients with Type III hyperlipoproteinemia and all 8 patients with lecithin-cholesterol-acyltransferase deficiency also had normal lipoprotein lipase values. These studies emphasize the necessity for differentiating between triglyceride lipase activity of hepatic and extrahepatic origin in evaluating patients with impaired triglyceride metabolism.
肝素后血浆脂解活性由两种水解活性组成,即肝甘油三酯脂肪酶和脂蛋白脂肪酶。通过硫酸铵沉淀以及分别使用共价连接肝素的琼脂糖和伴刀豆球蛋白A的亲和色谱法,将这两种酶分离并部分纯化。制备了针对肝甘油三酯脂肪酶的抗体,它们与脂蛋白脂肪酶无交叉反应。研究了选择性沉淀肝脂肪酶的最佳条件以及这两种脂肪酶的特异性测定方法。该方法应用于15例高甘油三酯血症患者和8例家族性卵磷脂 - 胆固醇 - 酰基转移酶缺乏症患者的研究,其中6例患者血浆甘油三酯浓度也显著升高。所有患者的肝血浆脂肪酶值均正常。所有8例I型和4例V型高脂蛋白血症患者中的2例脂蛋白脂肪酶活性明显降低。III型高脂蛋白血症患者和所有8例卵磷脂 - 胆固醇 - 酰基转移酶缺乏症患者的脂蛋白脂肪酶值也正常。这些研究强调了在评估甘油三酯代谢受损患者时区分肝源性和肝外源性甘油三酯脂肪酶活性的必要性。