Archer J A, Gorden P, Roth J
J Clin Invest. 1975 Jan;55(1):166-74. doi: 10.1172/JCI107907.
With insulin at 0.1 ng/ml, the binding of (125I)insulin in vitro to circulating lymphocytes from 11 obese patients was less than that observed with cells from 10 thin volunteers. Furthermore, with obese cells, unlabeled insulin was less effective in competing with labeled hormone for binding, both at low and high concentrations of unlabeled insulin. These differences were not accounted for by the high concentrations of insulin in the circulation of the obese patients at the time fthe blood was drawn, or by differences in degradation of hormone, or in the characteristics of the cell population. The decrease in binding appears to be due to a lowering of the receptor concentration, but some loss of affinity has not been excluded. Institution of a calorie restricted diet (nine patients) which ameliorated the hyperinsulinemia, produced an improvement in hormone binding. Since the insulin receptors of lymphocytes in metabolic disorders seem to reflect the state of insulin receptors or target cells such as liver and fat, the lymphocytes or other leukocytes appear to be ideal for studies of impaired cell responsiveness to hormones in man.
胰岛素浓度为0.1纳克/毫升时,11名肥胖患者循环淋巴细胞的体外(125I)胰岛素结合量低于10名瘦志愿者细胞的结合量。此外,对于肥胖患者的细胞,无论未标记胰岛素的浓度高低,未标记胰岛素与标记激素竞争结合的效果都较差。这些差异不能用采血时肥胖患者循环中高浓度的胰岛素来解释,也不能用激素降解差异或细胞群体特征差异来解释。结合量的降低似乎是由于受体浓度降低,但尚未排除亲和力的一些损失。实施热量限制饮食(9名患者)改善了高胰岛素血症,使激素结合情况得到改善。由于代谢紊乱患者淋巴细胞的胰岛素受体似乎反映了肝脏和脂肪等胰岛素受体或靶细胞的状态,淋巴细胞或其他白细胞似乎是研究人体细胞对激素反应受损的理想对象。