Sheehan D M, Young M
Endocrinology. 1979 May;104(5):1442-6. doi: 10.1210/endo-104-5-1442.
The equilibrium binding of diethylstilbestrol (DES) and 17 beta-estradiol (E2) to plasma proteins has been characterized. DES exhibits a 10- to 20-fold greater binding affinity index for bovine serum albumin and rat plasma than E2. As expected, E2 gave high values for binding to plasma from pregnant mice or rats, reflecting the presence of alpha-fetoprotein. DES bound to these samples as it did to bovine albumin and rat plasma. These results suggested that DES ineracts weakly with alpha-fetoprotein. This was verified by Scatchard plots of DES and E2 binding to rat and human pregnancy plasma. High affinity, low capacity binding was demonstrated with E2 but not with DES. The significantly lower binding of DES suggests that increased delivery of DES to the fetus may be at least partially responsible for the transplacental toxicity and carcinogenicity of DES.
已对己烯雌酚(DES)和17β-雌二醇(E2)与血浆蛋白的平衡结合进行了表征。DES对牛血清白蛋白和大鼠血浆的结合亲和力指数比E2高10至20倍。正如预期的那样,E2与怀孕小鼠或大鼠的血浆结合值很高,这反映了甲胎蛋白的存在。DES与这些样品的结合情况与它和牛白蛋白及大鼠血浆的结合情况相同。这些结果表明DES与甲胎蛋白的相互作用较弱。通过DES和E2与大鼠及人类妊娠血浆结合的Scatchard图验证了这一点。E2表现出高亲和力、低容量结合,而DES则没有。DES的结合显著较低,这表明DES向胎儿的递送增加可能至少部分是DES经胎盘毒性和致癌性的原因。