Tsukamoto I, Kojo S
Department of Food Science and Nutrition, Nara Women's University, Japan.
Gut. 1989 Mar;30(3):387-90. doi: 10.1136/gut.30.3.387.
The increase in activities of hepatic thymidylate synthetase (EC 2.1.1.45) and thymidine kinase (EC 2.7.1.21), which catalyse the formation of thymidylate through the de novo and salvage pathways, respectively, were significantly suppressed during liver regeneration in rats which were given glucocorticoids (hydrocortisone and dexamethasone) or indomethacin. These drugs also prevented the augment of hepatic DNA content in 24 h regenerating liver.
在给予糖皮质激素(氢化可的松和地塞米松)或吲哚美辛的大鼠肝脏再生过程中,催化分别通过从头合成途径和补救途径形成胸苷酸的肝胸苷酸合成酶(EC 2.1.1.45)和胸苷激酶(EC 2.7.1.21)的活性增加受到显著抑制。这些药物还阻止了24小时再生肝脏中肝DNA含量的增加。