Horie M, Iwasawa Y, Satoh T, Shimizu A, Nagata Y, Kamei T
Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd., Japan.
Biochem Pharmacol. 1993 Jul 20;46(2):297-305. doi: 10.1016/0006-2952(93)90418-v.
Caco-2 cells grown on membrane filters were used as a model to study the effects of NB-598, an inhibitor of squalene epoxidase, on cholesterol absorption from the intestinal epithelia. NB-598 (10 microM) inhibited the synthesis of sterol and sterol ester from [14C]acetate without affecting the synthesis of other lipids such as phospholipids (PL), free fatty acids (FFA) and triacylglycerol (TG). When labeled lipid was apically loaded as a micellar lipid solution into Caco-2 cell cultures, NB-598 reduced basolaterally secreted radioactivity in cholesterol, cholesterol ester, PL and TG. Furthermore, NB-598 suppressed the basolateral secretion of apolipoprotein (apo) B. When microsomes prepared from control Caco-2 cells were incubated with 10 microM NB-598, acyl CoA:cholesterol acyltransferase (ACAT) activity was inhibited slightly. After incubating Caco-2 cells with 10 microM NB-598, a slight reduction in cellular ACAT activity was also observed. These results suggest that suppression of the secretion of particles containing apo B and reduction of cellular ACAT activity in the intestinal epithelia are part of the mechanism of the cholesterol-lowering effect of NB-598.
以生长在膜滤器上的Caco-2细胞作为模型,研究角鲨烯环氧酶抑制剂NB-598对肠道上皮细胞胆固醇吸收的影响。NB-598(10微摩尔)抑制了[14C]乙酸盐合成固醇和固醇酯,而不影响其他脂质如磷脂(PL)、游离脂肪酸(FFA)和三酰甘油(TG)的合成。当将标记脂质作为胶束脂质溶液从顶端加载到Caco-2细胞培养物中时,NB-598降低了胆固醇、胆固醇酯、PL和TG从基底外侧分泌的放射性。此外,NB-598抑制了载脂蛋白(apo)B的基底外侧分泌。当用10微摩尔NB-598孵育从对照Caco-2细胞制备的微粒体时,酰基辅酶A:胆固醇酰基转移酶(ACAT)活性受到轻微抑制。在用10微摩尔NB-598孵育Caco-2细胞后,也观察到细胞ACAT活性略有降低。这些结果表明,抑制含apo B颗粒的分泌以及降低肠道上皮细胞的ACAT活性是NB-598降低胆固醇作用机制的一部分。