一种快速、灵敏、可靠的抑制素生物活性测定方法。

V. Lee, N. Colvin, H. Quigg, L. Atley, J. McMaster, L. Leversha, H. Burger
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引用次数: 5

摘要

描述了一种基于未成熟雌性大鼠垂体细胞FSH分泌的抑制素生物活性的快速2天定量分析。与先前建立的垂体FSH细胞含量测定相比,生物测定具有更陡的斜率,更高的精度和更高的灵敏度(四倍)。整个垂体腺用于制备垂体细胞,细胞分散的方法需要用胰蛋白酶进行单酶处理。将细胞(每孔180000个活细胞)放入含有抑制素的培养基中,孵育48小时。取出培养基,用放射免疫法检测FSH。以羊膜睾丸液制剂为标准,连续25次实验的抑制素剂量反应曲线的精密度指数为-0.08(平均值)[范围为-0.04 ~ -0.17],芬尼G值为0.017[0.003 ~ 0.06]。平均ED40为每孔0.17单位抑制素活性,在剂量-反应曲线的这一点上,测定间的变化为16.2%。该试验的实际容量为400个孔,允许测量至少40个未知数的剂量-反应曲线,每个剂量有三个剂量点和三个孔。该试验对几种动物中含有抑制素的制剂具有特异性。总的来说,该检测方法简单、精确、敏感,表明其适用于抑制素生物活性低的抑制素样品的测量以及抑制素纯化过程中大量组分的筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rapid, sensitive and reliable assay for inhibin bioactivity.
A rapid 2-day quantitative assay for inhibin bioactivity based on FSH secretion from pituitary cells of immature female rats is described. The bioassay exhibited steeper slopes, improved precision and greater (fourfold) sensitivity compared with a previously established pituitary FSH cell content assay. Whole pituitary glands were used for the preparation of pituitary cells and the method for cell dispersion required a single enzymatic treatment with trypsin. Cells (180,000 viable cells per well) were dispensed into culture media containing inhibin and incubated for 48 h. Media were removed and assayed for FSH by radioimmunoassay. Using a ram rete testis fluid preparation as standard the inhibin dose-response curves of 25 consecutive experiments showed indices of precision of -0.08(mean)[range -0.04 to -0.17] and Finney's G values of 0.017[0.003-0.06]. The mean ED40 was 0.17 units of inhibin activity per well with interassay variation of 16.2% at this point of the dose-response curve. The assay had a practical capacity of 400 wells, permitting the measurement of dose-response curves of at least 40 unknowns with three dose points and triplicate wells per dose. The assay is specific for inhibin-containing preparations from several animal species. Overall, the assay is simple, precise, and sensitive, indicative of its applicability to the measurement of inhibin samples with low inhibin bioactivity and to the screening of large numbers of fractions during inhibin purification.
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