Tongiani R, Piazzolla S, Paolicchi A
Istituto di Patologia Generale, Universita di Pisa, Italy.
Biochem Biophys Res Commun. 1990 Jan 30;166(2):801-6. doi: 10.1016/0006-291x(90)90880-v.
Metyrapone, an inhibitor of cytochrome P-450-dependent monooxygenases, enhanced the induction of tyrosine aminotransferase by dexamethasone in primary cultures of hepatocytes, while it had no effect on the basal level of the enzyme activity in the absence of the hormone. The amplification of the hormonal induction of tyrosine aminotransferase activity was strictly correlated with the concentration and with the inhibitory action of the compound on cytochrome P-450. The phenomenon occurred even at the maximally effective concentrations of dexamethasone, thus showing that metyrapone is a 'Glucocorticoid Potency Amplifier'. The dexamethasone activity amplification by metyrapone could be the consequence of a modulation of the glucocorticoid biotransformations due to the cytochrome P-450 inhibitor.
甲吡酮是一种细胞色素P - 450依赖性单加氧酶抑制剂,它能增强地塞米松对原代肝细胞中酪氨酸转氨酶的诱导作用,而在无该激素的情况下,它对该酶活性的基础水平没有影响。酪氨酸转氨酶活性的激素诱导放大作用与该化合物的浓度及其对细胞色素P - 450的抑制作用密切相关。即使在地塞米松的最大有效浓度下也会出现这种现象,因此表明甲吡酮是一种“糖皮质激素效能增强剂”。甲吡酮对地塞米松活性的增强可能是由于细胞色素P - 450抑制剂对糖皮质激素生物转化的调节所致。