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7-脱氢胆固醇与固醇载体蛋白的结合及维生素D3效应。

Binding of 7-dehydrocholesterol to sterol carrier protein and vitamin D3 effect.

作者信息

Takase S, Oizumi K, Moriuchi S, Hosoya N

出版信息

J Nutr Sci Vitaminol (Tokyo). 1975;21(6):387-94. doi: 10.3177/jnsv.21.387.

Abstract

It was confirmed that delta 5,7-sterol delta 7-reductase activity was suppressed by cholecalciferol (vitamin D3) in the enzyme system consisted of microsomes and sterol carrier protein (SCP). The enzyme activity was significantly decreased in the combination with microsomes obtained from either vitamin D-deficient or vitamin D3-treated rat liver and with SCP obtained from vitamin D3-treated rat. It was also demonstrated by the binding assay of the dextran-charcoal technique that 7-dehydrocholesterol binding to SCP could be specifically displaced by vitamin D3. The inhibition of cholecalciferol on 7-dehydrocholesterol binding to liver SCP was confirmed to be non-competitive inhibition.

摘要

已证实,在由微粒体和固醇载体蛋白(SCP)组成的酶系统中,胆钙化醇(维生素D3)可抑制δ5,7 - 固醇δ7 - 还原酶的活性。当与来自维生素D缺乏或经维生素D3处理的大鼠肝脏的微粒体以及来自经维生素D3处理的大鼠的SCP结合时,酶活性显著降低。通过葡聚糖 - 活性炭技术的结合试验还表明,维生素D3可特异性取代7 - 脱氢胆固醇与SCP的结合。胆钙化醇对7 - 脱氢胆固醇与肝脏SCP结合的抑制作用被确认为非竞争性抑制。

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