Hiramatsu K, Sakai H, Arimori S
Tokai J Exp Clin Med. 1980 Apr;5(2):137-45.
The effects of lipoproteins on 125I-insulin binding activity of mononuclear leukocytes were investigated in 22 diabetic patients and eight healthy adults. There was a significant negative relationship between insulin binding activity and levels of plasma beta-lipoprotein (r = 0.70, p < 0.01). The inhibition of insulin binding activity was also observed by in vitro addition of LDL to the assay system of insulin binding activity of mononuclear leukocytes. Double fluorescent staining techniques demonstrated that insulin receptors and LDL receptors are located very close to each other on the cell-surface. These results indicate that LDL intereferes with insulin binding activity in mononuclear leukocytes in vivo and in vitro, presumably because of the close localization of receptors for insulin and LDL on the cell surface. It is concluded that hyperlipoproteinemia is responsible for the decrease in insulin binding activity in diabetic patients.
在22名糖尿病患者和8名健康成年人中研究了脂蛋白对单核白细胞125I-胰岛素结合活性的影响。胰岛素结合活性与血浆β-脂蛋白水平之间存在显著负相关(r = 0.70,p < 0.01)。在单核白细胞胰岛素结合活性检测系统中体外添加低密度脂蛋白(LDL)也观察到胰岛素结合活性受到抑制。双重荧光染色技术表明胰岛素受体和LDL受体在细胞表面彼此位置非常接近。这些结果表明,LDL在体内和体外都会干扰单核白细胞中的胰岛素结合活性,推测这是由于胰岛素和LDL的受体在细胞表面位置接近所致。得出的结论是,高脂蛋白血症是糖尿病患者胰岛素结合活性降低的原因。