Bakke O, Eik-Nes K B
J Steroid Biochem. 1982 Nov;17(5):489-93. doi: 10.1016/0022-4731(82)90006-1.
The human cell line NHIK 3025 has a cytoplasmic dexamethasone receptor. When these cells are exposed to glucocorticoids, the cell cycle time is prolonged. The structural requirements for this effect were investigated by measuring cell number after 4 days exposure to different glucocorticoid analogues at concentrations of 10(-6) M and 10(-7) M. Growth inhibition at 10(-7) M required the 4-5 double bond, the 3,20 ketone--and the 11 beta, 17 alpha and 21 hydroxygroups of the glucocorticoid structure, e.g. cortisol, dexamethasone and prednisolone. Other synthetic glucocorticoids like bimetrazol and triamcinolone acetonide were also active at this dose whereas corticosterone, lacking the 17 alpha hydroxygroup, was only active at 10(-6) M. The effect was steroid specific and could be inhibited by anti-cortisol antiserum or by glucocorticoid antagonists.
人类细胞系NHIK 3025具有细胞质地塞米松受体。当这些细胞暴露于糖皮质激素时,细胞周期时间会延长。通过在10(-6)M和10(-7)M浓度下将细胞暴露于不同的糖皮质激素类似物4天后测量细胞数量,研究了这种效应的结构要求。在10(-7)M浓度下的生长抑制需要糖皮质激素结构的4-5双键、3,20-二酮以及11β、17α和21-羟基,例如皮质醇、地塞米松和泼尼松龙。其他合成糖皮质激素如双甲唑和曲安奈德在该剂量下也有活性,而缺乏17α-羟基的皮质酮仅在10(-6)M浓度下有活性。这种效应具有类固醇特异性,可被抗皮质醇抗血清或糖皮质激素拮抗剂抑制。