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鲨烯他汀1对甲羟戊酸途径脂质生物合成的影响。

Effect of squalestatin 1 on the biosynthesis of the mevalonate pathway lipids.

作者信息

Thelin A, Peterson E, Hutson J L, McCarthy A D, Ericsson J, Dallner G

机构信息

Department of Biochemistry, Stockholm University, Sweden.

出版信息

Biochim Biophys Acta. 1994 Dec 8;1215(3):245-9. doi: 10.1016/0005-2760(94)90049-3.

Abstract

The effects of squalestatin 1 on rat brain and liver homogenates and on Chinese hamster ovary tissue culture cells have been investigated. This compound effectively inhibits squalene biosynthesis in a highly selective manner. Cytoplasmic farnesyl pyrophosphate and geranylgeranyl pyrophosphate synthases are not affected, which is also the case for microsomal cis-prenyltransferase. In tissue culture cells, squalestatin 1 inhibits cholesterol biosynthesis completely, but does not alter dolichol synthesis or protein isoprenylation to a great extent. Incorporation of [3H]mevalonate into ubiquinone-9 and -10 increases 3-4-fold, probably as a result of increased synthesis of this lipid. Squalestatin 1 appears not only to be an effective inhibitor of cholesterol biosynthesis, but also to be more specific than other inhibitors used earlier in various in vitro and in vivo systems.

摘要

已对鲨烯抑素1对大鼠脑和肝匀浆以及对中国仓鼠卵巢组织培养细胞的作用进行了研究。该化合物以高度选择性的方式有效抑制鲨烯生物合成。细胞质法呢基焦磷酸合酶和香叶基香叶基焦磷酸合酶不受影响,微粒体顺式异戊二烯基转移酶也是如此。在组织培养细胞中,鲨烯抑素1完全抑制胆固醇生物合成,但在很大程度上不改变多萜醇合成或蛋白质异戊二烯化。[3H]甲羟戊酸掺入辅酶Q-9和-10增加了3至4倍,这可能是由于这种脂质合成增加所致。鲨烯抑素1似乎不仅是胆固醇生物合成的有效抑制剂,而且比早期在各种体外和体内系统中使用的其他抑制剂更具特异性。

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