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大鼠胆汁酸生物合成调节的生化位点。

Biochemical site of regulation of bile acid biosynthesis in the rat.

作者信息

Shefer S, Hauser S, Bekersky I, Mosbach E H

出版信息

J Lipid Res. 1970 Sep;11(5):404-11.

PMID:5501475
Abstract

The production of bile salts by rat liver is regulated by a feedback mechanism, but it is not known which enzyme controls endogenous bile acid synthesis. In order to demonstrate the biochemical site of this control mechanism, bile fistula rats were infused intravenously with (14)C-labeled bile acid precursors, and bile acid biosynthesis was inhibited as required by intraduodenal infusion of sodium taurocholate. The infusion of taurocholate (11-14 mg/100 g of rat per hr) inhibited the incorporation of acetate-1-(14)C, mevalonolactone-2-(14)C, and cholesterol-4-(14)C into bile acids by approximately 90%. In contrast, the incorporation of 7alpha-hydroxycholesterol-4-(14)C into bile acids was reduced by less than 10% during taurocholate infusion. These results indicate that the regulation of bile acid biosynthesis is exerted via cholesterol 7alpha-hydroxylase provided that hepatic cholesterol synthesis is adequate.

摘要

大鼠肝脏中胆汁盐的产生受反馈机制调节,但尚不清楚哪种酶控制内源性胆汁酸的合成。为了证明这种控制机制的生化位点,给胆瘘大鼠静脉注射(14)C标记的胆汁酸前体,并根据十二指肠内注射牛磺胆酸钠的需要抑制胆汁酸的生物合成。输注牛磺胆酸钠(每小时11 - 14毫克/100克大鼠)可使乙酸-1-(14)C、甲羟戊酸内酯-2-(14)C和胆固醇-4-(14)C掺入胆汁酸的量减少约90%。相比之下,在输注牛磺胆酸钠期间,7α-羟基胆固醇-4-(14)C掺入胆汁酸的量减少不到10%。这些结果表明,只要肝脏胆固醇合成充足,胆汁酸生物合成的调节是通过胆固醇7α-羟化酶实现的。

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