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固醇合成抑制剂。膳食中5α-胆甾-8(14)-烯-3β-醇-15-酮对肝脏胆固醇生物合成早期酶的影响。

Inhibitors of sterol synthesis. Effects of dietary 5 alpha-cholest-8(14)-en-3 beta-ol-15-one on early enzymes in hepatic cholesterol biosynthesis.

作者信息

Miller L R, Raulston D L, Schroepfer G J

机构信息

Department of Biochemistry, Rice University, Houston, TX 77251.

出版信息

Chem Phys Lipids. 1988 Jul;47(3):177-86. doi: 10.1016/0009-3084(88)90011-4.

Abstract

The effects of dietary administration (0.1% in diet for 8 days) of 5 alpha-cholest-8(14)-en-3 beta-ol-15-one on the levels of activity of cytosolic acetoacetyl coenzyme A thiolase, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase, and microsomal HMG-CoA reductase in liver have been studied in male Sprague-Dawley rats. Significant increases in the levels of activity of acetoacetyl-CoA thiolase and of HMG-CoA synthase were observed. The levels of microsomal HMG-CoA reductase activity were increased, relative to pair-fed control animals, in three experiments and increased, relative to ad libitum control animals, in one of three experiments. When compared with other agents for which the primary mode of action is an inhibition of the intestinal absorption of cholesterol, the magnitude of the increases in the levels of hepatic microsomal HMG-CoA reductase activity in the 15-ketosterol-fed rats was considerably smaller. In view of the previously described marked activity of the 15-ketosterol in the inhibition of the intestinal absorption of cholesterol, as well as its known effects in lowering HMG-CoA reductase activity in mammalian cells in culture, it is proposed that the 15-ketosterol may suppress the elevated levels of hepatic microsomal HMG-CoA reductase activity induced by the reduced delivery of cholesterol to liver as a consequence of the inhibition of the intestinal absorption of cholesterol.

摘要

在雄性斯普拉格-道利大鼠中,研究了日粮中添加5α-胆甾-8(14)-烯-3β-醇-15-酮(日粮中添加量为0.1%,持续8天)对肝脏中胞质乙酰乙酰辅酶A硫解酶、3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)合酶和微粒体HMG-CoA还原酶活性水平的影响。观察到乙酰乙酰辅酶A硫解酶和HMG-CoA合酶的活性水平显著增加。相对于配对饲喂的对照动物,在三个实验中微粒体HMG-CoA还原酶活性水平有所增加;相对于自由采食的对照动物,在三个实验中的一个实验中该活性水平增加。与主要作用方式为抑制胆固醇肠道吸收的其他药物相比,喂食15-酮甾醇的大鼠肝脏微粒体HMG-CoA还原酶活性水平的增加幅度要小得多。鉴于先前描述的15-酮甾醇在抑制胆固醇肠道吸收方面的显著活性,以及其在培养的哺乳动物细胞中降低HMG-CoA还原酶活性的已知作用,有人提出15-酮甾醇可能会抑制因胆固醇肠道吸收受抑制导致肝脏胆固醇供应减少而引起的肝脏微粒体HMG-CoA还原酶活性升高。

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