Koch B, Lutz-Bucher B, Briaud B, Mialhe C
Acta Endocrinol (Copenh). 1978 May;88(1):29-37. doi: 10.1530/acta.0.0880029.
The aim of this study was to determine whether pituitary glucocorticoid binding sites are under hormonal control. It was shown that corticosterone and thyroxine exerted antagonistic effects on both the transcortin-like component and true receptor present in the hypophysis: thyroid hormones, in contrast to glucocorticoids which exhibited opposite influence, increased maximum binding without affecting significantly the apparent association constant. Thus, it seems that the concentration of glucocorticoid binding sites is regulated by the glucocorticoid ligands, as well as by a different hormone. Moreover, a striking parallelism was found between plasma transcortin and pituitary transcotin-like capacity, argueing in favour of a plasma origin for this pituitary binder.
本研究的目的是确定垂体糖皮质激素结合位点是否受激素控制。结果表明,皮质酮和甲状腺素对垂体中存在的类运皮质素成分和真正受体均产生拮抗作用:与表现出相反影响的糖皮质激素不同,甲状腺激素增加了最大结合量,而对表观缔合常数没有显著影响。因此,糖皮质激素结合位点的浓度似乎受糖皮质激素配体以及另一种不同激素的调节。此外,血浆运皮质素与垂体类运皮质素能力之间发现了显著的平行关系,这表明这种垂体结合蛋白起源于血浆。