Sergeev P V, Semeĭkin A V, Dukhanin A S, Stonans E Iu
Eksp Klin Farmakol. 1994 May-Jun;57(3):20-2.
In in vivo and in vitro experiments, androgen anabolic steroid agents (testosterone, methandrostenolone) and dexamethasone showed a dose-dependent inhibition of PHA-stimulated proliferation of C57BL/6 mice thymocytes. The phytoecdysteroidal anabolic steroid ecdystene failed to inhibit thymocytic proliferation. The competitive radioligand analysis was used to show that testosterone and methandrostenolone displace the androgenic steroid mibolerone from lymphocytes. The findings provide evidence that lymphocytes have specific binding sites for androgen-anabolic steroids.
在体内和体外实验中,雄激素合成代谢类固醇药物(睾酮、大力补)和地塞米松对PHA刺激的C57BL/6小鼠胸腺细胞增殖呈剂量依赖性抑制。植物蜕皮甾体合成代谢类固醇蜕皮甾酮未能抑制胸腺细胞增殖。采用竞争性放射性配体分析表明,睾酮和大力补可从淋巴细胞中置换出雄激素类固醇米勃龙。这些发现证明淋巴细胞具有雄激素合成代谢类固醇的特异性结合位点。