Olefsky J M, Reaven G M
Endocrinology. 1975 Jun;96(6):1486-98. doi: 10.1210/endo-96-6-1486.
We have measured insulin binding to isolated adipocytes prepared from rats of varying ages and body weights. The ability of adipocytes to bind insulin progressively decreases as animals get older and fatter until about 70 days of age and 300 g body weight are reached. From this point on further decreases in insulin binding to adipocytes were not seen as rats got older and fatter. Analysis of the data indicated that this decrease in insulin binding could be accounted for by decreased numbers of insulin receptor sites per cell. Further studies were conducted in which animals were allowed to age, but obesity was prevented or reversed by hypocaloric diets. In these experiments decreased insulin binding was either prevented or restored to normal by the negative caloric state, indicating that age had no appreciable effect on the ability of adipocytes to bind insulin. The influence of the obesity associated variables-hyperinsulinemia and increased fat cell size-on insulin binding was also examined. These latter studies are consistent with the concept that elevated in vivo plasma insulin levels lead to decreased insulin receptors, and further suggest a role for additonal factors in regulating the adipocyte insulin receptor.
我们已测量胰岛素与从不同年龄和体重的大鼠制备的分离脂肪细胞的结合情况。随着动物年龄增长和体重增加,脂肪细胞结合胰岛素的能力逐渐下降,直至达到约70日龄和300克体重。从这一点起,随着大鼠年龄增长和体重增加,未观察到胰岛素与脂肪细胞结合的进一步下降。数据分析表明,胰岛素结合的这种下降可归因于每个细胞胰岛素受体位点数量的减少。进行了进一步研究,让动物衰老,但通过低热量饮食预防或逆转肥胖。在这些实验中,负热量状态可预防胰岛素结合下降或使其恢复正常,表明年龄对脂肪细胞结合胰岛素的能力没有明显影响。还研究了与肥胖相关的变量——高胰岛素血症和脂肪细胞大小增加——对胰岛素结合的影响。这些后期研究与体内血浆胰岛素水平升高导致胰岛素受体减少的概念一致,并进一步表明其他因素在调节脂肪细胞胰岛素受体方面的作用。