Huijmans J G, Degenhart H J, Kortleve D J, Visser H K
Acta Endocrinol (Copenh). 1981 Jun;97(2):243-50. doi: 10.1530/acta.0.0970243.
Several effects of hydroxylated sterols on cell cultures are known. Most of these can be explained by an inhibition of the cholesterol synthesis at the level of the 3-hydroxy-3-methylglutaryl CoA reductase. When studying cholesterol metabolism in rat adrenal cells, an inhibitory action of some sterols on the ACTH-stimulated corticosterone production was observed. The effects of one sterol, 22S-OH-cholesterol, were investigated further. The sterol had no effect on the ACTH-stimulated cyclic AMP production, suggesting an intact receptor-adenylate cyclase complex and cellular membrane. In the presence of ACTH and 22-OH-cholesterol particularly the free cholesterol concentration was elevated; 22S-OH-cholesterol therefore probably exerts its inhibitory effect at a step located after hydrolysis of the cholesterol esters. 22S-OH-cholesterol had no effect on the conversion of exogenous pregnenolone into corticosterone. These results make it probable, that the inhibitory effect of 22S-OH-cholesterol on the ACTH-stimulated corticosterone production is situated at the level of the cholesterol side-chain cleavage.
羟基化固醇对细胞培养的几种作用是已知的。其中大多数可以通过在3-羟基-3-甲基戊二酰辅酶A还原酶水平上抑制胆固醇合成来解释。在研究大鼠肾上腺细胞中的胆固醇代谢时,观察到某些固醇对促肾上腺皮质激素(ACTH)刺激的皮质酮产生具有抑制作用。对一种固醇,即22S-羟基胆固醇的作用进行了进一步研究。该固醇对ACTH刺激的环磷酸腺苷(cAMP)产生没有影响,这表明受体-腺苷酸环化酶复合物和细胞膜是完整的。在ACTH和22-羟基胆固醇存在的情况下,特别是游离胆固醇浓度升高;因此,22S-羟基胆固醇可能在胆固醇酯水解后的某个步骤发挥其抑制作用。22S-羟基胆固醇对外源性孕烯醇酮转化为皮质酮没有影响。这些结果表明,22S-羟基胆固醇对ACTH刺激的皮质酮产生的抑制作用可能位于胆固醇侧链裂解水平。