Nagashima H, Kumagai H, Tomoda H, Omura S
Exploratory Research Laboratories II, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan.
Life Sci. 1993;52(19):1595-600. doi: 10.1016/0024-3205(93)90060-g.
We have studied the in vivo inhibition of hepatic sterol biosynthesis by 1233A, a specific inhibitor of the enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase. Administration of the compound orally to mice resulted in a dose-dependent inhibition of [14C]acetate incorporation into sterols in liver, but did not exert any significant effect on [14C]mevalonate incorporation. The results indicate that the in vivo inhibition of sterol synthesis occurs only at pre-mevalonate enzymatic steps in the sterol biosynthetic pathway, thus being compatible with the presumed site of inhibition, HMG-CoA synthase. Moreover, owing to irreversible inactivation of the enzyme by 1233A, it was possible to detect in vivo effect on the enzyme by assays of its activity in cell-free extracts from livers; the drug-treatment also resulted in a similarly dose-dependent inhibition of HMG-CoA synthase activity. In contrast, acetoacetyl-CoA thiolase and HMG-CoA reductase, the enzymes also responsible for mevalonate synthesis in the pathway, did not show any significant change in activity. These results clearly demonstrate that the inhibition of hepatic sterol synthesis caused by 1233A is indeed due to selective inhibition of HMG-CoA synthase in the tissues.
我们研究了1233A(一种3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)合酶的特异性抑制剂)对肝脏甾醇生物合成的体内抑制作用。给小鼠口服该化合物导致肝脏中[14C]乙酸掺入甾醇的剂量依赖性抑制,但对[14C]甲羟戊酸掺入没有任何显著影响。结果表明,甾醇合成的体内抑制仅发生在甾醇生物合成途径中甲羟戊酸之前的酶促步骤,因此与推测的抑制位点HMG-CoA合酶相符。此外,由于1233A使该酶不可逆失活,通过测定肝脏无细胞提取物中的酶活性来检测其对该酶的体内作用成为可能;药物处理也导致HMG-CoA合酶活性出现类似的剂量依赖性抑制。相比之下,该途径中同样负责甲羟戊酸合成的乙酰乙酰辅酶A硫解酶和HMG-CoA还原酶的活性没有任何显著变化。这些结果清楚地表明,1233A引起的肝脏甾醇合成抑制确实是由于对组织中HMG-CoA合酶的选择性抑制。