Ikenaka K, Shirasaka T, Kitano S, Fujii S
Gan. 1979 Jun;70(3):353-9.
The effect of uracil on the metabolism of 5-fluorouracil (5-FU) in vitro was studied. 5-FU was mainly phosphorylated in intact Yoshida sarcoma cells, whereas it was mainly degraded in liver slices. Uracil inhibited degradation of 5-FU much more than its phosphorylation; incubation of 2,500 microM of uracil with 2.5 microM of 5-FU (molar ratio, 1,000:1) inhibited the degradation of 5-FU by 70%, but did not affect its phosphorylation. With homogenates of Yoshida sarcoma or liver uracil inhibited degradation of 5-FU greatly, phosphorylation of 5-FU by alpha-D-ribose 1-phosphate (RiblP) and ATP to some extent, and phosphorylation by 5-phospho-alpha-D-ribosyl diphosphate (PPRibP) very little. The activities of the enzymes involved in the metabolism of 5-FU in various tissues were also determined. Degradation of 5-FU was much faster in liver than in other tissues and was very slow in tumor tissue. Phosphorylation of 5-FU with RiblP and ATP was rapid in Yoshida sarcoma and bone marrow. Phosphoribosyltransferase activity was high in Yoshida sarcoma and thymus, but low in bone marrow.
研究了尿嘧啶对5-氟尿嘧啶(5-FU)体外代谢的影响。5-FU在完整的吉田肉瘤细胞中主要发生磷酸化,而在肝切片中主要发生降解。尿嘧啶对5-FU降解的抑制作用远大于其磷酸化作用;2500微摩尔的尿嘧啶与2.5微摩尔的5-FU(摩尔比为1000:1)共同孵育可使5-FU的降解受到70%的抑制,但不影响其磷酸化。在吉田肉瘤或肝脏的匀浆中,尿嘧啶极大地抑制了5-FU的降解,在一定程度上抑制了由α-D-核糖1-磷酸(RiblP)和ATP介导的5-FU磷酸化,而对由5-磷酸-α-D-核糖焦磷酸(PPRibP)介导的磷酸化抑制作用很小。还测定了不同组织中参与5-FU代谢的酶的活性。5-FU在肝脏中的降解比在其他组织中快得多,在肿瘤组织中则非常缓慢。在吉田肉瘤和骨髓中,由RiblP和ATP介导的5-FU磷酸化很快。磷酸核糖转移酶活性在吉田肉瘤和胸腺中较高,而在骨髓中较低。