Davidson M B
Metabolism. 1984 Jun;33(6):532-7. doi: 10.1016/0026-0495(84)90008-8.
Hyperinsulinemia was required to preserve normal intravenous glucose tolerance in late pregnancy in the rat (18 to 21 days' gestation). To evaluate the site and mechanism of this insulin resistance, insulin binding and action were measured in hepatocytes freshly isolated from control and gravid animals. As expected, glucose concentrations were lower, insulin levels were higher, and hepatocyte size increased in the pregnant animals. Insulin binding was similar in liver cells from the two groups. No difference was found in sensitivity or responsiveness of insulin-stimulated net 14C-glucose incorporation into glycogen in the hepatocytes from the control and gravid rats. These results suggest that the well-documented, but ill-defined, insulin antagonism of late pregnancy does not include the liver and is a postreceptor defect, most likely residing in muscle tissue.
在大鼠妊娠晚期(妊娠18至21天),需要高胰岛素血症来维持正常的静脉葡萄糖耐量。为了评估这种胰岛素抵抗的部位和机制,对从对照动物和妊娠动物新鲜分离的肝细胞中的胰岛素结合和作用进行了测量。正如预期的那样,妊娠动物的葡萄糖浓度较低,胰岛素水平较高,肝细胞大小增加。两组肝细胞中的胰岛素结合情况相似。在对照大鼠和妊娠大鼠的肝细胞中,胰岛素刺激的净14C-葡萄糖掺入糖原的敏感性或反应性没有差异。这些结果表明,妊娠晚期有充分记录但定义不明确的胰岛素拮抗作用不包括肝脏,是一种受体后缺陷,最有可能存在于肌肉组织中。