Pasanen M, Pelkonen O
Steroids. 1984 May;43(5):517-27. doi: 10.1016/s0039-128x(84)90156-9.
Cholesterol side-chain cleavage (CSCC) activity towards exogenous cholesterol was quantified by an one-step reversed-phase minicolumn method for the separation of pregnenolone formed in the reaction. The assay is rapid and reproducible. The method is linear for up to 2 mg of placental mitochondrial protein and up to 1 mg of bovine adrenal mitochondrial protein in the incubata over 30 min and 5 min reaction times, respectively. Average Km and Vmax values were 14.1 microM and 3.4 pmol/min/mg for the placental preparation and 1.5 microM and 20.7 pmol/min/mg for the bovine adrenal mitochondrial preparation. In human placenta, the mitochondrial fraction contained most of the CSCC activity. Inhibition studies showed that aminoglutethimide (500 microM) inhibited both placental and bovine adrenal activities at the same level (about 80-90% inhibition) but androstenedione (500 microM), metyrapone (500 microM), benzo(a)pyrene (800 microM) and Emulgen 911 (0.05%) were more effective in human placental preparations. Neither of the activities were inhibited to any great extent by alpha-naphthoflavone (500 microM), SKF 525A (500 microM) or 7-ethoxycoumarin (1 mM).
采用一步反相微柱法对反应中生成的孕烯醇酮进行分离,以此定量胆固醇侧链裂解(CSCC)对外源性胆固醇的活性。该测定方法快速且可重复。在分别为30分钟和5分钟的反应时间内,对于高达2毫克的胎盘线粒体蛋白和高达1毫克的牛肾上腺线粒体蛋白,该方法在孵育过程中呈线性关系。胎盘制剂的平均Km和Vmax值分别为14.1微摩尔和3.4皮摩尔/分钟/毫克,牛肾上腺线粒体制剂的平均Km和Vmax值分别为1.5微摩尔和20.7皮摩尔/分钟/毫克。在人胎盘中,线粒体部分含有大部分CSCC活性。抑制研究表明,氨鲁米特(500微摩尔)对胎盘和牛肾上腺的活性抑制程度相同(约80 - 90%抑制),但雄烯二酮(500微摩尔)、美替拉酮(500微摩尔)、苯并(a)芘(800微摩尔)和乳化剂911(0.05%)在人胎盘制剂中更有效。α - 萘黄酮(500微摩尔)、SKF 525A(500微摩尔)或7 - 乙氧基香豆素(1毫摩尔)均未对任何一种活性产生很大程度的抑制。