Nagata Y, Horie M, Hidaka Y, Yonemoto M, Hayashi M, Watanabe H, Ishida F, Kamei T
Central Research Laboratories, Banyu Pharmaceutical Co., Ltd., Tokyo, Japan.
Chem Pharm Bull (Tokyo). 1992 Feb;40(2):436-40. doi: 10.1248/cpb.40.436.
NB-598, a potent inhibitor of squalene epoxidase, inhibited cholesterol synthesis from [14C]acetate and induced intracellular squalene accumulation in Hep G2 cells. NB-598 inhibited cholesterol synthesis from [14C]acetate, [3H]mevalonate, and [3H]squalene, but not from [3H]2,3-oxidosqualene in Hep G2 cells. It reduced cholesterol ester synthesis remarkably in the absence of exogenous cholesterol. This compound did not have any effect on the synthesis of ubiquinone and dolichol. When Hep G2 cells were prelabeled with micellar [3H]cholesterol, NB-598 did not affect the excretion of bile acid incorporated from [3H]cholesterol. However, NB-598 decreased the secretion of free and esterified cholesterol, triacylglycerol, and phospholipids, and increased the secretion of squalene. NB-598 is thought not only to inhibit cholesterol synthesis, but also to inhibit the secretion of lipids.
NB - 598是一种有效的角鲨烯环氧酶抑制剂,可抑制Hep G2细胞中由[14C]乙酸盐合成胆固醇,并诱导细胞内角鲨烯积累。NB - 598抑制Hep G2细胞中由[14C]乙酸盐、[3H]甲羟戊酸和[3H]角鲨烯合成胆固醇,但不抑制由[3H]2,3 -氧化角鲨烯合成胆固醇。在没有外源性胆固醇的情况下,该化合物显著降低胆固醇酯的合成。这种化合物对泛醌和多萜醇的合成没有任何影响。当用胶束[3H]胆固醇对Hep G2细胞进行预标记时,NB - 598不影响从[3H]胆固醇掺入的胆汁酸的排泄。然而,NB - 598减少了游离胆固醇、胆固醇酯、三酰甘油和磷脂的分泌,并增加了角鲨烯的分泌。人们认为NB - 598不仅抑制胆固醇合成,还抑制脂质分泌。