Kono S, Merriam G R, Brandon D D, Loriaux D L, Lipsett M B, Fujino T
J Steroid Biochem. 1983 Jul;19(1B):627-33. doi: 10.1016/0022-4731(83)90228-5.
Plasma levels of 2-hydroxyestrone (2-OHE1) and 2-hydroxyestradiol (2-OHE2) were determined by a new radioimmunoassay which employed a short Sephadex LH-20 column chromatography for the purification of samples and the antiserum to 2-hydroxyestrone-17-(O-carboxymethyl)oxime-BSA conjugate for assay. The plasma value was below the detection limit for the assay (approximately 15 pg/ml) in men and non-pregnant women, but rose 20-200 pg/ml during pregnancy in 2-OHE1 and around 15 pg/ml in the 3rd trimester of pregnancy in 2-OHE2. There was no significant difference of plasma 2-OHE1 level between normal pregnancy and toxemic pregnancy with hypertension, in the 3rd trimester. The plasma level was very low in all of three subjects with the placental dysfunction in toxemic pregnancy. The plasma metabolic clearance rate (MRCp) of 2-OHE1 and 2-OHE2 were determined in normal adults by two methods; infusion of unlabeled 2-OHE1 and 2-OHE2 to equilibrium with radioimmunoassay of their plasma levels, and infusion of [3H]-2-OHE1 and [3H]-2-OHE2 to equilibrium with measurement of chromatographically purified their tritium. The MCRs by the former and latter methods was 40-70 X 10(3) and 15-50 X 10(3) in 2-OHE1, and 18-29 X 10(3) and 12-14 X 10(3) l/day in 2-OHE2, respectively. The major plasma metabolite comigrated with 2-methoxy compounds to each catecholestrogen. The t1/2 of disappearance rate by the method of infusion of unlabeled compounds was approx. 45 s in 2-OHE1 and 90 s in 2-OHE2. When [3H]-2-OHE1 and [3H]-2-OHE2 were incubated with blood samples of adults, 2-methoxy compounds also rapidly formed. From these results it is concluded that the extremely high MCRp of 2-OHE1 and 2-OHE2 make it unlikely these compounds circulate peripherally except in pregnancy in levels sufficient to produce the physiological effects on estrogen receptors or catecholamines.
采用一种新的放射免疫分析法测定血浆中2-羟雌酮(2-OHE1)和2-羟雌二醇(2-OHE2)的水平,该方法采用短的葡聚糖凝胶LH-20柱色谱法纯化样品,并使用针对2-羟雌酮-17-(O-羧甲基)肟-BSA偶联物的抗血清进行检测。男性和非妊娠女性的血浆值低于该检测方法的检测限(约15 pg/ml),但在孕期2-OHE1升高至20 - 200 pg/ml,2-OHE2在妊娠晚期升至约15 pg/ml。妊娠晚期,正常妊娠与高血压中毒性妊娠的血浆2-OHE1水平无显著差异。中毒性妊娠中所有三名胎盘功能不全的受试者血浆水平都非常低。通过两种方法测定正常成年人中2-OHE1和2-OHE2的血浆代谢清除率(MRCp);输注未标记的2-OHE1和2-OHE2至平衡状态并通过放射免疫分析法测定其血浆水平,以及输注[3H]-2-OHE1和[3H]-2-OHE2至平衡状态并通过测量色谱纯化后的氚来测定。2-OHE1通过前一种和后一种方法的MCR分别为40 - 70×10(3)和15 - 50×10(3),2-OHE2分别为18 - 29×10(3)和12 - 14×10(3) l/天。主要的血浆代谢物与每种儿茶酚雌激素的2-甲氧基化合物共迁移。通过输注未标记化合物的方法测定的消失率的t1/2,2-OHE1约为45秒,2-OHE2约为90秒。当[3H]-2-OHE1和[3H]-2-OHE2与成年人的血样孵育时,也会迅速形成2-甲氧基化合物。从这些结果可以得出结论,2-OHE1和2-OHE2极高的MRCp使得这些化合物除了在孕期外,不太可能以足以对雌激素受体或儿茶酚胺产生生理作用的水平在外周循环。