Kawashima M, Kamiyoshi M, Tanaka K
Endocrinology. 1987 Feb;120(2):582-8. doi: 10.1210/endo-120-2-582.
In the hen, the preoptic area, medial basal hypothalamus, and anterior lobe of the pituitary showed a greater uptake of [3H]estradiol-17 beta (E2) in vivo than other tissues. This uptake was decreased when unlabeled diethylstilbestrol was injected together with the [3H]E2 or when unlabeled E2 was injected before the [3H]E2 injection. A specific estrogen binding component having properties of a receptor was found in vitro in both soluble and insoluble fractions of these tissues in a hypotonic buffer solution. The administration of E2 in vivo caused a marked decrease in the estrogen receptor binding in the soluble fraction with a concomitant increase in binding in the insoluble fraction; as a result, total binding (sum of the bindings in soluble and insoluble fraction) did not change.
在母鸡体内,视前区、下丘脑内侧基底部和垂体前叶对[3H]雌二醇-17β(E2)的摄取量比其他组织更高。当未标记的己烯雌酚与[3H]E2一起注射,或在注射[3H]E2之前注射未标记的E2时,这种摄取量会降低。在低渗缓冲溶液中,在这些组织的可溶性和不溶性部分均发现了具有受体特性的特异性雌激素结合成分。体内给予E2会导致可溶性部分的雌激素受体结合显著减少,同时不溶性部分的结合增加;结果,总结合量(可溶性和不溶性部分结合量之和)没有变化。