Kim Y S, Yoon Y J, Jatoi I, Kim Y
Am J Obstet Gynecol. 1981 Jan;139(1):27-32. doi: 10.1016/0002-9378(81)90406-3.
Fetal macrosomia in diabetic pregnancy has been shown to accompany increases in the fetal levels of deoxyribonucleic acid (DNA) and proteins in animal model systems. In order to elucidate the underlying mechanisms of this macrosomia, the synthesis of DNA and proteins, the transport of the precursors, and the tissue level of DNA polymerase activities in macrosomic fetuses from mildly diabetic rats were compared with those in normal fetuses on 20.5 and 19.5 days of gestation. Increases in the influx of precursors and stimulation of synthesis of the macromolecules were observed in macrosomic fetuses as early as 19.5 days of gestation. However, stimulation of DNA polymerase activities in macrosomic fetuses did not occur until 20.5 days of gestation. Therefore, stimulation of DNA polymerase may participate in maintenance of macrosomia but does not initiate macrosomia. Whether or not increases in both the influx of substrates and the synthesis activities precede the macrosomia has yet to be determined.
在动物模型系统中,糖尿病妊娠中的巨大胎儿已被证明伴随着胎儿脱氧核糖核酸(DNA)和蛋白质水平的升高。为了阐明这种巨大胎儿的潜在机制,将轻度糖尿病大鼠的巨大胎儿在妊娠20.5天和19.5天时的DNA和蛋白质合成、前体物质的转运以及DNA聚合酶活性的组织水平与正常胎儿进行了比较。早在妊娠19.5天时,就观察到巨大胎儿的前体物质流入增加和大分子合成受到刺激。然而,巨大胎儿的DNA聚合酶活性直到妊娠20.5天时才受到刺激。因此,DNA聚合酶的刺激可能参与维持巨大胎儿状态,但并非引发巨大胎儿的原因。底物流入和合成活性的增加是否先于巨大胎儿的出现尚待确定。