Pullinger C R, Gibbons G F
J Lipid Res. 1983 Oct;24(10):1321-8.
The true rate of sterol synthesis in liver cells was determined by measurement of the weight of desmosterol produced over a given time period during incubations in the presence of triparanol. The simultaneous presence of tritiated water (3H2O) during the incubations permitted a direct observation of the weight of tritium incorporated into a given mass of newly synthesized sterol. The incorporation of tritium per atom of sterol carbon (H/C ratio) was lower than some previously reported values and suggests that a sizeable proportion of the reducing equivalents (NADPH) required for sterol synthesis arises via the pentose phosphate pathway. The H/C ratio changed significantly with length of the incubation period. The value of the ratio was also dependent upon whether the acetyl-CoA units utilized for sterol synthesis were derived predominantly from a carbohydrate or a fatty acid source.
通过测量在三苯乙醇存在下孵育特定时间段内产生的胆甾烯醇重量,确定肝细胞中甾醇合成的真实速率。孵育过程中同时存在氚水(3H2O),使得能够直接观察到掺入给定质量新合成甾醇中的氚重量。每个甾醇碳原子的氚掺入量(H/C比)低于一些先前报道的值,这表明甾醇合成所需的相当一部分还原当量(NADPH)是通过磷酸戊糖途径产生的。H/C比随孵育时间的长短而显著变化。该比值还取决于用于甾醇合成的乙酰辅酶A单位主要来自碳水化合物还是脂肪酸来源。