首页> 外文期刊>The Journal of Clinical Investigation: The Official Journal of the American Society for Clinical Investigation >Increasing dietary cholesterol induces different regulation of classic and alternative bile acid synthesis.
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Increasing dietary cholesterol induces different regulation of classic and alternative bile acid synthesis.

机译:增加膳食胆固醇会诱导经典和替代胆汁酸合成的不同调节。

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摘要

We investigated the effect of increasing dietary cholesterol on bile acid pool sizes and the regulation of the two bile acid synthetic pathways (classic, via cholesterol 7alpha-hydroxylase, and alternative, via sterol 27-hydroxylase) in New Zealand white rabbits fed 3 g cholesterol/per day for up to 15 days. Feeding cholesterol for one day increased hepatic cholesterol 75 and cholesterol 7alpha-hydroxylase activity 1.6 times without significant change of bile acid pool size or sterol 27-hydroxylase activity. After three days of cholesterol feeding, the bile acid pool size increased 83 (P < 0.01), and further feeding produced 10-20 increments, whereas cholesterol 7alpha-hydroxylase activity declined progressively to 60 below baseline. In contrast, sterol 27-hydroxylase activity rose 58 after three days of cholesterol feeding and remained elevated with continued intake. Bile drainage depleted the bile acid pool and stimulated downregulated cholesterol 7alpha-hydroxylase activity but did not affect sterol 27-hydroxylase activity. Thus, increasing hepatic cholesterol does not directly inhibit cholesterol 7alpha-hydroxylase and initially favors enzyme induction, whereas increased bile acid pool is the most powerful inhibitor of cholesterol 7alpha-hydroxylase. Sterol 27-hydroxylase is insensitive to the bile acid flux but is upregulated by increasing hepatic cholesterol.
机译:我们研究了增加膳食胆固醇对胆汁酸池大小的影响以及两种胆汁酸合成途径(经典,通过胆固醇 7α-羟化酶,另一种,通过甾醇 27-羟化酶)的调节,在新西兰大白兔中每天喂食 3 克胆固醇,持续长达 15 天。喂食一天胆固醇使肝胆固醇增加75%,胆固醇7α-羟化酶活性增加1.6倍,胆汁酸池大小或甾醇27-羟化酶活性没有显着变化。胆固醇喂养3 d后,胆汁酸池大小增加了83%(P < 0.01),进一步喂养后增加了10%-20%,而胆固醇7α-羟化酶活性逐渐下降到基线以下的60%。相比之下,胆固醇喂养三天后,甾醇 27-羟化酶活性上升了 58%,并且随着持续摄入而保持升高。胆汁引流耗尽胆汁酸池并刺激下调胆固醇7α-羟化酶活性,但不影响甾醇27-羟化酶活性。因此,增加肝脏胆固醇不会直接抑制胆固醇7α-羟化酶,最初有利于酶诱导,而增加胆汁酸池是胆固醇7α-羟化酶最有效的抑制剂。甾醇 27-羟化酶对胆汁酸通量不敏感,但因肝胆固醇升高而上调。

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