Raoux R J, Maume B F
C R Seances Soc Biol Fil. 1984;178(1):84-91.
The use of aminoglutethimide at 5.10(-4) mol/l, inhibitor of endogenous steroidogenesis, and of exogenous progesterone (20 micrograms/ml) as substrate allowed the control of the steroid 21-hydroxylating reaction in cultured newborn rat adrenocortical cells. This method has been employed to show that the 21-hydroxylation by these cells is strongly induced by the adrenocorticotropic hormone (20 mU/ml).
使用浓度为5×10⁻⁴摩尔/升的氨鲁米特(内源性类固醇生成抑制剂)和外源性孕酮(20微克/毫升)作为底物,可以控制培养的新生大鼠肾上腺皮质细胞中的类固醇21-羟化反应。该方法已被用于表明这些细胞的21-羟化作用受到促肾上腺皮质激素(20毫单位/毫升)的强烈诱导。