Vizethum W, Ruzicka T, Goerz G
Chem Biol Interact. 1980 Aug;31(2):215-9. doi: 10.1016/0009-2797(80)90008-3.
The influence of systemic application of chemically unrelated drugs and xenobiotics (phenobarbital (PB), rifampicin (Rifa), pregnenolone-16 alpha-carbonitrile (PCN) and 3-methylcholanthrene (MC) on drug metabolizing enzymes was investigated in the skin of rats of both sexes. The results were compared with those obtained in the liver. PB, Rifa and PCN induced the aryl hydrocarbon hydroxylase (AHH) in the skin though to a lesser extent than MC. The basal enzymic activity as well as the inducibility were considerably lower in the skin than in the liver. The activity of cytochrome c reductase was similar in all rats independently from the pretreatment. Only slight sex differences were noted: generally, the activity was higher in males. Cytochrome P-450 content of the skin could not be detected as well as various dealkylation activities.
研究了全身应用化学结构不相关的药物和外源性物质(苯巴比妥(PB)、利福平(Rifa)、孕烯醇酮 - 16α - 腈(PCN)和3 - 甲基胆蒽(MC))对雌雄大鼠皮肤中药物代谢酶的影响。将结果与在肝脏中获得的结果进行了比较。PB、Rifa和PCN诱导了皮肤中的芳烃羟化酶(AHH),但其诱导程度低于MC。皮肤中的基础酶活性以及诱导性均显著低于肝脏。无论预处理如何,所有大鼠中细胞色素c还原酶的活性相似。仅观察到轻微的性别差异:一般来说,雄性的活性较高。皮肤中细胞色素P - 450的含量以及各种脱烷基活性均未检测到。