Quérat B, Hardy A, Leloup-Hâtey J
Gen Comp Endocrinol. 1985 Sep;59(3):482-93. doi: 10.1016/0016-6480(85)90408-3.
Testosterone (T) and 17 beta-estradiol (E2) plasma levels and metabolic clearance rates (MCR) were measured to investigate their ovarian production in immature silver eel. The dynamics of T and E2 metabolism were studied in catheterized eels using single injections of 0.2 to 0.5 microCi 3H-labeled steroid. The distribution volumes, biological half-life and MCR of nonconjugated tracers were calculated on the basis of a two-compartment model. At the end of the experiments, radioactivity was measured in different organs and tissues to localize the site of T and E2 catabolism. The volume of the inner compartment was 3.4% for T and E2. The outer compartment was larger for T (6.4%) than that for E2 (4.3%). The biological half-life was three to four times shorter for T (14.5 hr) than that for E2 (48.5 hr). The MCR for T (1.71 ml/kg body wt/hr) was higher than for E2 (0.51 ml/kg body wt/hr). Plasma levels were determined, using radioimmunoassay, on samples taken before injections of radiolabeled steroid. Free or protein-bound hormone levels were 0.12 and 0.31 ng/ml for T and E2, respectively. Conjugated T and E2 levels were, respectively, 0.13 and 0.23 ng/ml. Production rates were determined as the product of the MCR and the plasma concentration of the nonconjugated hormone. No significant differences were observed between the production rates of T and E2 (0.24 ng/kg body wt/hr). The liver was the principal site of metabolism for both hormones, which were excreted via the enterohepatic route. E2 injection gave rise to no metabolite in the plasma whereas after T injection a metabolite was produced, the concentration of which increased as a function of time. Its chromatographic properties were different from that of E2 or androstenedione, suggesting that no significant peripheral aromatization or 17-oxidoreduction occurs in the immature silver eel.
测量了睾酮(T)和17β-雌二醇(E2)的血浆水平及代谢清除率(MCR),以研究它们在未成熟银鳗中的卵巢生成情况。在通过导管插入的鳗鱼中,使用单次注射0.2至0.5微居里的3H标记类固醇来研究T和E2的代谢动态。基于二室模型计算了非结合示踪剂的分布容积、生物半衰期和MCR。实验结束时,测量了不同器官和组织中的放射性,以确定T和E2分解代谢的部位。T和E2的内室容积均为3.4%。T的外室(6.4%)比E2的外室(4.3%)大。T的生物半衰期(14.5小时)比E2的生物半衰期(48.5小时)短三到四倍。T的MCR(1.71毫升/千克体重/小时)高于E2的MCR(0.51毫升/千克体重/小时)。使用放射免疫分析法测定了注射放射性标记类固醇之前采集的样本的血浆水平。T和E2的游离或与蛋白质结合的激素水平分别为0.12和0.31纳克/毫升。结合型T和E2的水平分别为0.13和0.23纳克/毫升。生成率被确定为MCR与非结合激素血浆浓度的乘积。T和E2的生成率之间未观察到显著差异(0.24纳克/千克体重/小时)。肝脏是这两种激素的主要代谢部位,它们通过肠肝途径排泄。注射E2后血浆中未产生代谢物,而注射T后产生了一种代谢物,其浓度随时间增加。其色谱特性与E2或雄烯二酮不同,这表明在未成熟银鳗中未发生显著的外周芳香化或17-氧化还原反应。