Super D M, Palmquist D L, Schanbacher F L
J Dairy Sci. 1976 Aug;59(8):1409-13. doi: 10.3168/jds.S0022-0302(76)84378-0.
A routine laboratory assay to evaluate relative concentrations of lipoprotein lipase activator (apo C-II) in cow serum was developed. The assay was linear for at least 120 min after an initial, unexplained, lag ime of 13 to 15 min. Half-maximal activation was in the range of 1 to 2% serum in the assay. Inhibition of activation was indicated at high amounts (10%) of serum. Activation from plasma was half that from serum, presumably caused by an increase in substrate Km in the presence of heparin. Use of glyceryl tri[9,10-3H] oleate yielded excessively high blanks; [2-3H] glyceryl triolein is suggested for routine assay. Relative amounts of activator were not different between dry and lactating cows fed "conventional" diets. Activator concentration increased linearly with increasing dietary fat and was related to concentration of total lipid in plasma. The assay may provide a useful adjunct in studies on lipoprotein metabolism.
开发了一种用于评估牛血清中脂蛋白脂肪酶激活剂(载脂蛋白C-II)相对浓度的常规实验室检测方法。该检测方法在最初13至15分钟无法解释的延迟时间后至少120分钟呈线性。在该检测中,半数最大激活在1%至2%血清范围内。高浓度(10%)血清显示出激活抑制。血浆的激活量是血清的一半,推测是由于在肝素存在下底物Km增加所致。使用甘油三[9,10-3H]油酸酯产生的空白值过高;建议使用[2-3H]甘油三油酸酯进行常规检测。饲喂“常规”日粮的干奶牛和泌乳奶牛之间激活剂的相对含量没有差异。激活剂浓度随日粮脂肪增加呈线性增加,且与血浆中总脂质浓度相关。该检测方法可能为脂蛋白代谢研究提供有用的辅助手段。