Blázquez E, Perez Castillo A, Alvarez E
Horm Metab Res. 1986 Oct;18(10):666-71. doi: 10.1055/s-2007-1012402.
The studies described in this paper were undertaken to characterize the hepatic insulin receptors in liver membranes and isolated hepatocytes, during rat ontogenic development. In liver membranes insulin binding was found to be the same in fetal and greater in suckling rats as compared with adult animals. Modifications of insulin binding reflect changes in the number of receptors, but not in the affinity constants. Time courses of insulin association and dissociation from liver membranes were unaffected by development. Degradation of insulin by liver membranes was significantly lower in fetal than in adult rats, but this does not seem to be responsible for the differences observed in binding. No significant differences in the degradation of insulin receptors between different groups of liver membranes were found. Similar results were obtained with isolated hepatocytes except for a reduced number of insulin receptors in fetal cells. This could be explained by the smaller cell surface of younger cells, since when the results were expressed by micron 2, insulin binding was almost the same in fetal and adult rats. These findings suggest that the early hepatic development of insulin receptors may play a significant role in the metabolic growth processes of the fetus and in the availability of nutrients after birth.
本文所述研究旨在表征大鼠个体发育过程中肝细胞膜和分离的肝细胞中的肝胰岛素受体。在肝细胞膜中,发现胎儿期的胰岛素结合情况与成年动物相比,在胎儿期相同,在哺乳期大鼠中更高。胰岛素结合的改变反映了受体数量的变化,而非亲和常数的变化。胰岛素与肝细胞膜结合和解离的时间进程不受发育影响。肝细胞膜对胰岛素的降解在胎儿期明显低于成年大鼠,但这似乎不是观察到的结合差异的原因。不同组肝细胞膜之间胰岛素受体的降解没有显著差异。分离的肝细胞也得到了类似结果,只是胎儿细胞中的胰岛素受体数量减少。这可以用较年轻细胞较小的细胞表面来解释,因为当结果以微米²表示时,胎儿和成年大鼠的胰岛素结合几乎相同。这些发现表明,胰岛素受体的早期肝脏发育可能在胎儿的代谢生长过程以及出生后营养物质的可利用性方面发挥重要作用。