Rotsztejn W H, Normand M, Lalonde J, Fortier C
Endocrinology. 1975 Jul;97(1):223-30. doi: 10.1210/endo-97-1-223.
The amount of corticosterone bound to proteins in the adenohypophysis and dorsal hippocampus was studied concurrently with the plasma ACTH concentration in 4-week adrenalectomized male rats under steady-state conditions achieved by infusing the steroid at a constant rate for 45 min. Corticosterone binding was measured by gel chromatography on Sephadex LH-20, using a TE buffer containing 0.4 m NaCl. No saturation was observed in whole homogenates and supernatants with increasing plasma corticosterone concentrations. However, corticosterone binding by the pituitary and by one of two types of hippocampal receptors evidenced saturation within our range of corticosterone infusion rates, indeed. Scatchard plots allowed us to distinguish two types of binding sites in the hippocampus. The first, saturated at a low corticosterone concentration has an association constant of 3.0 times 10-8 M-1 with a number of binding sites estimated at 150 times 10- minus 15 mol/mg protein, whereas the second is associated with non-specific binding. The adenohypophysis shows only one kind of binding site with an association constant of 3.6 times 10-8 m- minus 1 and a number of sites estimated at 989 times 10- minus 15 mol/mg protein. A suggestive relationship was observed between ACTH inhibition by corticosterone and saturation of the pituitary binding sites. Our data are consistent with the possible involvement of corticosterone binding by specific sites in the negative feedback regulation of ACTH release.
在4周龄肾上腺切除的雄性大鼠中,通过以恒定速率输注类固醇45分钟达到稳态条件,同时研究腺垂体和背侧海马中与蛋白质结合的皮质酮量与血浆促肾上腺皮质激素(ACTH)浓度的关系。使用含有0.4 m NaCl的TE缓冲液,通过Sephadex LH - 20凝胶色谱法测量皮质酮结合。随着血浆皮质酮浓度增加,在全匀浆和上清液中未观察到饱和现象。然而,在我们的皮质酮输注速率范围内,垂体和两种海马受体之一的皮质酮结合确实显示出饱和。Scatchard图使我们能够区分海马中的两种结合位点。第一种在低皮质酮浓度下饱和,其结合常数为3.0×10⁻⁸ M⁻¹,结合位点数估计为150×10⁻¹⁵ mol/mg蛋白质,而第二种与非特异性结合相关。腺垂体仅显示一种结合位点,其结合常数为3.6×10⁻⁸ M⁻¹,位点数估计为989×10⁻¹⁵ mol/mg蛋白质。观察到皮质酮对ACTH的抑制与垂体结合位点的饱和之间存在提示性的关系。我们的数据与特定位点的皮质酮结合可能参与ACTH释放的负反馈调节一致。