Lerario A C, Wajchenberg B L, el-Andere W, Ohnuma L Y, Monaci J, Sankowsky M, Toledo I T, Souza E, Germek O
Diabetes. 1985 Aug;34(8):780-6. doi: 10.2337/diab.34.8.780.
Insulin binding to erythrocytes was sequentially studied in 12 healthy pregnant women during the anabolic (11-22 wk) and the catabolic (31-38 wk) gestational phases. For comparison, we studied 12 nonpregnant subjects at mid-luteal and mid-follicular menstrual phases. Oral glucose tolerance tests were also performed during these studies. There was a progressive worsening of the glucose tolerance from the anabolic to the catabolic phase associated with fasting hypoglycemia and hyperinsulinemia. The worsening of glucose tolerance was accompanied by a progressive increment of insulin secretion. Insulin binding to red blood cells increased progressively from the anabolic to the catabolic phase, due to an increased number of receptors per cell, associated with a reduction in the apparent affinity at the low occupancy levels. We concluded that the insulin resistance of pregnancy was not accompanied by an impaired binding of insulin to its receptors, at least in the RBC. The data suggest that the defect of insulin action lies at a site distal to the receptor.
在12名健康孕妇的合成代谢期(妊娠11 - 22周)和分解代谢期(妊娠31 - 38周),对胰岛素与红细胞的结合情况进行了系列研究。作为对照,我们研究了12名处于月经周期黄体中期和卵泡中期的非妊娠受试者。在这些研究过程中还进行了口服葡萄糖耐量试验。从合成代谢期到分解代谢期,葡萄糖耐量逐渐恶化,伴有空腹低血糖和高胰岛素血症。葡萄糖耐量的恶化伴随着胰岛素分泌的逐渐增加。胰岛素与红细胞的结合从合成代谢期到分解代谢期逐渐增加,这是由于每个细胞上的受体数量增加,同时在低占据水平下表观亲和力降低。我们得出结论,至少在红细胞中,妊娠的胰岛素抵抗并不伴有胰岛素与其受体结合受损。数据表明胰岛素作用缺陷位于受体远端的位点。