Holmquist L, Carlson L A
Acta Med Scand. 1987;222(1):15-21. doi: 10.1111/j.0954-6820.1987.tb09922.x.
The lecithin:cholesterol acyltransferase (LCAT) activity of lipoprotein depleted normal and fish eye disease (FED) plasma was assayed in a modified Glomset-Wright incubation system where the enzyme was allowed to act on three different normal lipoprotein substrates consisting of an authentic mixture of very low (VLDL), low (LDL) and high (HDL) density lipoproteins to assay total LCAT activity, HDL to assay alpha-LCAT activity and combined VLDL and LDL to assay beta-LCAT activity, respectively. However, using normal plasma depleted of HDL, leaving its combined VLDL and LDL as enzyme substrate, resulted in a more than twofold increase in the LCAT activity of FED plasma from the two patients compared to the activity obtained with HDL present in the incubation mixture, indicating an inhibitory effect of HDL on the beta-LCAT activity present in FED plasma. This inhibitory effect of normal HDL could also be demonstrated by autoincubation of FED plasma mixed with isolated HDL2 or HDL3. Both these HDL subfractions had a pronounced inhibitory effect on the cholesteryl ester formation in FED plasma. The present study thus clearly demonstrates that normal HDL inhibits the beta-LCAT activity present in FED plasma, esterifying the free cholesterol of combined VLDL and LDL, derived from controls as well as from the two FED patients.
在改良的格洛姆塞特-赖特孵育系统中,测定了脂蛋白去除的正常血浆和鱼眼病(FED)血浆中卵磷脂:胆固醇酰基转移酶(LCAT)的活性。在该系统中,使该酶作用于三种不同的正常脂蛋白底物,分别为由极低密度(VLDL)、低密度(LDL)和高密度(HDL)脂蛋白的真实混合物组成的底物来测定总LCAT活性,用HDL来测定α-LCAT活性,用VLDL和LDL的混合物来测定β-LCAT活性。然而,使用去除HDL的正常血浆,将其VLDL和LDL的混合物作为酶底物,与在孵育混合物中存在HDL时获得的活性相比,两名FED患者的FED血浆中LCAT活性增加了两倍多,这表明HDL对FED血浆中存在的β-LCAT活性具有抑制作用。将FED血浆与分离的HDL2或HDL3混合后进行自孵育,也可证明正常HDL的这种抑制作用。这两种HDL亚组分对FED血浆中胆固醇酯的形成均有明显的抑制作用。因此,本研究清楚地表明,正常HDL抑制FED血浆中存在的β-LCAT活性,使来自对照组以及两名FED患者的VLDL和LDL混合物中的游离胆固醇酯化。