Berry E M, Ziv E, Bar-On H
Diabetologia. 1980;19(6):535-40. doi: 10.1007/BF00253181.
Protein and glycoprotein synthesis and secretion by isolated perfused livers and isolated hepatocytes from control and streptozotocin diabetic rats have been investigated. (3)H-Leucine and (14)C-glucosamine incorporation were used as markers for protein and glycoprotein synthesis and secretion. Total protein secretion was reduced by 50% in the perfusate (p < 0.001) and by 36% in hepatocytes (p < 0.05), but glycoprotein secretion was unchanged in both preparations from diabetic animals. These differences were not due to changes in the available pool sizes of the different labels. On liver fractionation, all membrane components from the liver of diabetic animals had lowered (3)H-leucine: (14)Cd-glucosamine ratios in relation to the control animals. This was caused by enhanced glucosamine incorporation in relation to that of leucine. It is suggested that whereas protein synthesis is decreased in acutely diabetic rats, the production of glycoproteins is normal and occurs by the same pathway as in control animals.
对来自对照大鼠和链脲佐菌素诱导的糖尿病大鼠的离体灌注肝脏及离体肝细胞的蛋白质和糖蛋白合成与分泌进行了研究。采用(3)H-亮氨酸和(14)C-葡糖胺掺入作为蛋白质和糖蛋白合成与分泌的标志物。灌注液中总蛋白分泌减少了50%(p < 0.001),肝细胞中减少了36%(p < 0.05),但糖尿病动物的两种制剂中糖蛋白分泌均未改变。这些差异并非由于不同标记物的可用池大小变化所致。对肝脏进行分级分离时,与对照动物相比,糖尿病动物肝脏的所有膜成分中(3)H-亮氨酸:(14)C-葡糖胺的比率均降低。这是由于葡糖胺掺入相对于亮氨酸掺入增加所致。提示在急性糖尿病大鼠中,虽然蛋白质合成减少,但糖蛋白的产生正常,且与对照动物通过相同途径发生。