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机构地区:[1]北京医科大学第一医院妇产科
出 处:《生殖医学杂志》1994年第2期73-75,共3页Journal of Reproductive Medicine
摘 要:采用体外放射配体受体结合法测定3-酮-地索高诺酮(KDG)与兔子宫胞浆雌激素受体(EcR)、孕激素受体(PcR)和大鼠腹侧前列腺胞浆雄激素受体(AcR)结合的亲和力,并以左旋18-甲基炔诺酮(LNG)作对照,从受体水平探讨KDG对当体激素受体的选择性。结果表明:KDG对PcR有很高的亲和力,是LNG的1.5倍;对AcR的亲和力很低,仅为LNG的0.74倍;对EcR几乎没有亲和力,受体亲和力选择系数也明显高于LNG。由此可见,在LNG甾核结构中C11位引入次甲基合成的KDG,其受体亲和力选择性更专一。Radio-ligand binding assay(RLBA)in vitro was applied to measure the relative bindingaffinity(RBA)of 3-keto-desogestrel(KDG) with estrogen and progestogen receptors (EcR、 PcR)inrabbit uterine cytosol and androgen receptor(AcR)in rat ventral prostate cytosol,in com=p,drisoii xvI tlilevonorgestrel(LNG)。 ResuIts indicated that RBA of KDG for PcR was very high, which was 1.5 timesthat of LNG;RBA of KDG for AcR was low,wmch was0.74times than that of LNG;KDG had almostunmeasurable affinity for EcR。 Selectivity index for receptor affinity (RBA-PcR/RBA-AcR) of KDGwas remarkably higher than that of LNG。It is suggested that KDG would be a more specific progestogenthan LNG by the addition of methylene at the position of C11 of steroid ring。
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