Tsutsumi K, Inoue Y, Hagi A, Murase T
Nutrition Research Laboratory, Otsuka Pharmaceutical Factory, Tokushima, Japan.
Metabolism. 1997 Mar;46(3):257-60. doi: 10.1016/s0026-0495(97)90250-x.
Lipoprotein lipase (LPL) and cholesteryl ester transfer protein (CETP) are determinants of high-density lipoprotein (HDL) cholesterol concentrations in plasma. We have previously reported that NO-1886, by increasing LPL activity, causes elevation of HDL cholesterol levels in rats. In the present study, we studied the effect of NO-1886 on CETP activity in experimental animals. Since previous reports suggest that rats may lack CETP, we examined hamsters and rabbits, as well as rats. We found that NO-1886 increased LPL activity, resulting in elevation of plasma HDL cholesterol in all three animals. We confirmed that rats lack CETP and that both hamsters and rabbits have high CETP activity. NO-1886 had no effect on CETP activity in hamsters and rabbits. These results demonstrate that the compound NO-1886 elevates HDL cholesterol in experimental animals by selectively increasing LPL activity without any effect on CETP. Animals with low CETP and high LPL activities appear to be more sensitive to NO-1886 than those with high CETP and low LPL activities.
脂蛋白脂肪酶(LPL)和胆固醇酯转运蛋白(CETP)是血浆中高密度脂蛋白(HDL)胆固醇浓度的决定因素。我们之前报道过,NO-1886通过增加LPL活性,使大鼠的HDL胆固醇水平升高。在本研究中,我们研究了NO-1886对实验动物CETP活性的影响。由于之前的报道表明大鼠可能缺乏CETP,我们对仓鼠、兔子以及大鼠进行了检测。我们发现,NO-1886增加了LPL活性,导致所有这三种动物的血浆HDL胆固醇升高。我们证实大鼠缺乏CETP,而仓鼠和兔子都具有较高的CETP活性。NO-1886对仓鼠和兔子的CETP活性没有影响。这些结果表明,化合物NO-1886通过选择性增加LPL活性而升高实验动物的HDL胆固醇,对CETP没有任何影响。与CETP活性高而LPL活性低的动物相比,CETP活性低而LPL活性高的动物似乎对NO-1886更为敏感。