Stĕpán J, Ferwerda W, Lojda Z
Acta Univ Carol Med Monogr. 1977(78 Pt 2):41-50.
Extrahepatic bile flow obstruction is followed by a several-fold increase in alkaline phosphatase activity in the liver. This activity passes into the blood. The increase in the activity of the enzyme in the liver can be prevented by inhibitors of RNA and protein synthesis. Inducible alkaline phosphatase was purified from rat liver and 1,000-fold purification was achieved. The incorporation of labbelled precursors (14C amino acids and 14C glucosamine) into the liver alkaline phosphatase was evaluated. No significant difference were found between specific alkaline phosphatase activities and specific radioactivities in the control rats and rats with 7.30 h after bile duct obstruction. The incorporation of 14C-amino acids into the total liver proteins was 20% lower in rats with cholestasis than in the control group. The results are evidence that the liver is the source of elevated alkaline phosphatase activity in serum in cholestasis, and that the production of alkaline phosphatase in the liver is prevented by inhibitors of RNA a protein synthesis. However, the enzyme might be synthesized before the 14C-labelled precursors were applied.
肝外胆汁流梗阻后,肝脏碱性磷酸酶活性会增加数倍。这种活性会进入血液。RNA和蛋白质合成抑制剂可阻止肝脏中该酶活性的增加。从大鼠肝脏中纯化出了可诱导的碱性磷酸酶,实现了1000倍的纯化。评估了标记前体(14C氨基酸和14C葡糖胺)掺入肝脏碱性磷酸酶的情况。在对照大鼠和胆管梗阻7.30小时后的大鼠中,特异性碱性磷酸酶活性和特异性放射性之间未发现显著差异。胆汁淤积大鼠肝脏总蛋白中14C氨基酸的掺入量比对照组低20%。结果证明,肝脏是胆汁淤积时血清中碱性磷酸酶活性升高的来源,并且RNA和蛋白质合成抑制剂可阻止肝脏中碱性磷酸酶的产生。然而,该酶可能在应用14C标记前体之前就已合成。