Xu G, Salen G, Shefer S, Tint G S, Kren B T, Nguyen L B, Steer C J, Chen T S, Salen L, Greenblatt D
Medical Service, Veterans Affairs Medical Center, East Orange, New Jersey, USA.
Gastroenterology. 1997 Dec;113(6):1958-65. doi: 10.1016/s0016-5085(97)70016-7.
BACKGROUND & AIMS: Cholesterol feeding unexpectedly inhibits cholesterol 7 alpha-hydroxylase in rabbits. The aim of this study was to explore the mechanism.
Twenty male New Zealand white rabbits were fed regular chow with and without 2% cholesterol for 10 days followed by 7 days of bile drainage. The activities of hepatic cholesterol 7 alpha-hydroxylase and sterol 27-hydroxylase that control bile acid synthesis in classic and alternative pathways were related to the size and composition of bile acid pool.
After feeding cholesterol, plasma and hepatic cholesterol concentrations increased, the bile acid pool doubled (from 254 +/- 44 to 533 +/- 51 mg; P < 0.001), cholesterol 7 alpha-hydroxylase activity decreased 68% (P < 0.01), but sterol 27-hydroxylase activity increased 66% (P < 0.05) with increased cholic acid synthesis (P < 0.01). Bile drainage in the cholesterol-fed rabbits depleted the bile acid pool and stimulated down-regulated cholesterol 7 alpha-hydroxylase activity 11.4-fold (P < 0.001), although hepatic cholesterol remained elevated. Hepatic sterol 27-hydroxylase activity was unaffected.
Feeding cholesterol increased hepatic cholesterol and stimulated sterol 27-hydroxylase and alternative bile acid synthesis, which expanded the bile acid pool and inhibited cholesterol 7 alpha-hydroxylase in rabbits. In distinction, hepatic sterol 27-hydroxylase was insensitive to changes in the bile acid pool.
给兔子喂食胆固醇意外地抑制了胆固醇7α-羟化酶。本研究旨在探究其机制。
20只雄性新西兰白兔分别喂食含2%胆固醇和不含胆固醇的常规饲料10天,随后进行7天的胆汁引流。经典途径和替代途径中控制胆汁酸合成的肝胆固醇7α-羟化酶和甾醇27-羟化酶的活性与胆汁酸池的大小和组成相关。
喂食胆固醇后,血浆和肝脏胆固醇浓度升高,胆汁酸池增加一倍(从254±44毫克增至533±51毫克;P<0.001),胆固醇7α-羟化酶活性降低68%(P<0.01),但甾醇27-羟化酶活性增加66%(P<0.05),同时胆酸合成增加(P<0.01)。胆固醇喂养组兔子的胆汁引流耗尽了胆汁酸池,并刺激下调的胆固醇7α-羟化酶活性增加11.4倍(P<0.001),尽管肝脏胆固醇仍保持升高。肝脏甾醇27-羟化酶活性未受影响。
喂食胆固醇增加了肝脏胆固醇,并刺激了甾醇27-羟化酶和替代胆汁酸合成,这扩大了胆汁酸池并抑制了兔子的胆固醇7α-羟化酶。相比之下,肝脏甾醇27-羟化酶对胆汁酸池的变化不敏感。