Kappy M S, Plotnick L
J Clin Endocrinol Metab. 1980 Dec;51(6):1440-6. doi: 10.1210/jcem-51-6-1440.
Insulin binding studies in obese patients have been limited to adults due to the relative inaccessibility to tissues for study in the pediatric age group. Insulin binding to the erythrocytes (RBCs) of 9 obese pre-pubertal children, 8 obese adolescents, and 10 obese adults was studied. There was a mean decrease of 15% of insulin binding in the obese patients (P < 0.02 vs. controls). Calculation of receptor concentrations by means of Scatchard plots showed a mean 30% reduction in insulin receptors on the RBCs of obese patients as a group (P < 0.001 vs. controls). The binding of insulin and receptor concentration were inversely proportional to the fasting plasma insulin concentration (= -0.60 and -0.44, respectively). These correlations were significant (P < 0.001 and P < 0.05, respectively). The mean empty site receptor affinity (Ke) was significantly increased in obese patients, but only partially compensated for the loss of receptors with respect to total insulin bound over the physiological range of insulin concentrations. The results of binding studies in the obese adults were similar to those in the children and adolescents, and agreed with published reports of insulin binding in obese adults using adipocytes or monocytes as the source of insulin receptors. The observed decrease in insulin binding to the RBCs of obese children and adolescents correlated with fasting hyperinsulinemia and, therefore, may contribute to the etiology of the insulin resistance or glucose intolerance observed in these patients.
由于儿科年龄组的组织相对难以获取用于研究,肥胖患者的胰岛素结合研究一直局限于成年人。对9名肥胖青春期前儿童、8名肥胖青少年和10名肥胖成年人的红细胞(RBC)进行了胰岛素结合研究。肥胖患者的胰岛素结合平均下降了15%(与对照组相比,P < 0.02)。通过Scatchard图计算受体浓度显示,肥胖患者组的红细胞上胰岛素受体平均减少30%(与对照组相比,P < 0.001)。胰岛素结合和受体浓度与空腹血浆胰岛素浓度呈负相关(分别为 = -0.60和 -0.44)。这些相关性具有统计学意义(分别为P < 0.001和P < 0.05)。肥胖患者的平均空位点受体亲和力(Ke)显著增加,但在胰岛素浓度的生理范围内,相对于结合的总胰岛素,仅部分补偿了受体的损失。肥胖成年人的结合研究结果与儿童和青少年相似,并且与使用脂肪细胞或单核细胞作为胰岛素受体来源的肥胖成年人胰岛素结合的已发表报告一致。观察到的肥胖儿童和青少年红细胞胰岛素结合减少与空腹高胰岛素血症相关,因此可能有助于这些患者胰岛素抵抗或葡萄糖不耐受的病因学研究。