Saintonge J, Côté R
Pediatr Res. 1984 Jul;18(7):650-3. doi: 10.1203/00006450-198407000-00017.
Fetal brain development was investigated near term in guinea pigs rendered diabetic with streptozotocin. The liver and the placenta were used as reference organs. Compared to controls, those fetuses from diabetic animals had normal cerebrum and cerebellum weights, but higher liver and placenta weights in relation to fetal weights. Although liver and placenta cell number (DNA content) was unchanged, it was significantly increased in the fetal cerebrum and cerebellum of diabetics. Although the tissue protein concentration was decreased in the liver and the placenta, it was unchanged and even increased in the cerebrum and cerebellum, respectively. The concentration of myelin (cerebroside-sulfatide) was unchanged in the cerebrum, but it was increased in the cerebellum of diabetic animals. These data suggest that diabetes has a growth-promoting effect on the fetal brain cell number. Furthermore, differences in the protein content between fetal organs may reflect abnormalities in protein metabolism which do not affect the brain during diabetic pregnancies.
用链脲佐菌素使豚鼠患糖尿病,在孕期接近足月时对其胎儿大脑发育情况进行了研究。肝脏和胎盘用作参照器官。与对照组相比,糖尿病动物的胎儿大脑和小脑重量正常,但相对于胎儿体重而言,肝脏和胎盘重量更高。虽然肝脏和胎盘的细胞数量(DNA含量)未变,但糖尿病动物胎儿的大脑和小脑中该含量显著增加。虽然肝脏和胎盘的组织蛋白浓度降低,但大脑和小脑的蛋白浓度分别未变甚至升高。大脑中髓磷脂(脑苷脂 - 硫脂)的浓度未变,但糖尿病动物小脑的髓磷脂浓度升高。这些数据表明,糖尿病对胎儿脑细胞数量有促进生长的作用。此外,胎儿器官之间蛋白质含量的差异可能反映了蛋白质代谢异常,而这种异常在糖尿病妊娠期间不会影响大脑。