Aringer L, Eneroth P
J Lipid Res. 1973 Sep;14(5):563-72.
The microsomal fraction and the 18,000 g supernatant fluid obtained from livers from normal rats, cholestyraminetreated rats, or from rats with a bile fistula have been used to compare the 7alpha-hydroxylation of [4-(14)C]cholesterol and beta-[4-(14)C]sitosterol (24alpha-ethyl-cholesterol). It was not possible to increase the specific formation of 7alpha-hydroxy-beta-sitosterol above 0.05% with any of the preparations. This conversion was less than 1% of that found for cholesterol. The inhibitory effect of added 7-oxo- and 7beta-hydroxy-beta-sitosterol on the 7alpha-hydroxylation of cholesterol was found to be much less than that of the corresponding cholesterol compounds. 7alpha-Hydroxy-beta-sitosterol was without effect. It is concluded that the activity of the cholesterol 7alpha-hydroxylase is dependent upon the structure of the steroid side chain.
从正常大鼠、消胆胺处理的大鼠或有胆瘘的大鼠肝脏中获得的微粒体部分和18,000 g上清液,已用于比较[4-(14)C]胆固醇和β-[4-(14)C]谷甾醇(24α-乙基胆固醇)的7α-羟化作用。用任何一种制剂都不可能将7α-羟基-β-谷甾醇的比生成量提高到0.05%以上。这种转化不到胆固醇转化量的1%。发现添加的7-氧代-β-谷甾醇和7β-羟基-β-谷甾醇对胆固醇7α-羟化的抑制作用远小于相应的胆固醇化合物。7α-羟基-β-谷甾醇没有作用。得出的结论是,胆固醇7α-羟化酶的活性取决于甾体侧链的结构。