Panin L E, Ostanina L S, Kolpakov A R
Vopr Med Khim. 1995 Nov-Dec;41(6):12-6.
The existence of common epitope in insulin molecule and apolipoprotein B one was shown by means of enzyme immunoassay. Similar epitopes were revealed in apoB-containing lipoproteins (VLDL and LDL) by dot-immunobinding and immunoelectroblotting. Epitopes locate on the surface of lipoproteins and are not screened by lipids. The existence of common epitopes is the reason of competition between insulin and LDL. The experiments with isolated perfused rat hindquarter demonstrate that insulin increased the glucose uptake by muscle and LDL decreased it. Simultaneous perfusion with LDL and insulin leads to reduced insulin action due to completion for insulin receptors. After the recovery of S-S bounds apoB forms some proteins, containing common epitopes with insulin. The presence of such proteins was shown in lipoprotein-free serum. Apoprotein B and its derivates seem to be insulin antagonists with marked antiinsulin action.
通过酶免疫测定法证实了胰岛素分子和载脂蛋白B1中存在共同表位。通过斑点免疫结合和免疫电印迹法在含载脂蛋白B的脂蛋白(极低密度脂蛋白和低密度脂蛋白)中发现了类似的表位。表位位于脂蛋白表面,未被脂质屏蔽。共同表位的存在是胰岛素与低密度脂蛋白之间竞争的原因。对离体灌注大鼠后肢的实验表明,胰岛素增加肌肉对葡萄糖的摄取,而低密度脂蛋白则降低其摄取。同时灌注低密度脂蛋白和胰岛素会由于对胰岛素受体的竞争而导致胰岛素作用减弱。二硫键恢复后,载脂蛋白B形成一些与胰岛素含有共同表位的蛋白质。在无脂蛋白血清中显示出此类蛋白质的存在。载脂蛋白B及其衍生物似乎是具有明显抗胰岛素作用的胰岛素拮抗剂。