Jia X C, Kessel B, Yen S S, Tucker E M, Hsueh A J
J Clin Endocrinol Metab. 1986 Jun;62(6):1243-9. doi: 10.1210/jcem-62-6-1243.
A sensitive in vitro assay based on the stimulation of estrogen production by cultured rat granulosa cells was recently developed for the measurement of biologically active FSH. This bioassay system is specific for FSH, highly sensitive, and capable of measuring basal FSH levels in rat serum. The granulosa cell aromatase bioassay was improved by the use of additives known to enhance FSH activity and by pretreatment of serum with 12% polyethylene glycol to remove inhibitory substances. We applied this method to the measurement of bioactive FSH levels in serum samples from human subjects. As determined in daily blood samples during ovulatory menstrual cycles in seven women, bioactive FSH levels exhibited a pattern closely resembling that of immunoreactive FSH. The mean bioactive serum FSH levels were 29.9, 20.5, 39.2, and 14.8 mIU/ml for the early follicular phase, late follicular phase, preovulatory surge, and luteal phase, respectively. The bio- to immunoratio (B:I) throughout the menstrual cycle ranged from 1.4-3.4, with a mean of 2.5. The ratios for early follicular phase, late follicular phase, preovulatory surge, and luteal phase were 2.7, 2.3, 1.4, and 2.6, respectively. The correlation coefficient (r) of the serum FSH values obtained by bioassay and RIA was 0.91. FSH bioactivity was also measured in patients in each of the following categories with the following mean values: oral contraceptive pill users (undetectable), hypothalamic amenorrhea (18.7 mIU/ml; B:I, 2.6), premature ovarian failure (163 mIU/ml; B:I, 1.7), and postmenopausal women (191 mIU/ml; B:I, 1.6). These findings suggest that measurement of immunoreactive FSH levels correctly reflects the biological activity of FSH in serum of cycling women and patients in certain hyper- and hypogonadotropic states. The granulosa cell aromatase bioassay represents a new tool for future assessments of biologically active FSH in physiological and pathophysiological conditions.
最近开发了一种基于培养的大鼠颗粒细胞刺激雌激素产生的灵敏体外测定法,用于测量生物活性促卵泡激素(FSH)。该生物测定系统对FSH具有特异性,高度灵敏,并且能够测量大鼠血清中的基础FSH水平。通过使用已知可增强FSH活性的添加剂以及用12%聚乙二醇预处理血清以去除抑制物质,改进了颗粒细胞芳香化酶生物测定法。我们将此方法应用于测量人类受试者血清样本中的生物活性FSH水平。在7名女性排卵性月经周期的每日血样中测定发现,生物活性FSH水平呈现出与免疫反应性FSH极为相似的模式。卵泡早期、卵泡晚期、排卵前高峰和黄体期的生物活性血清FSH平均水平分别为29.9、20.5、39.2和14.8 mIU/ml。整个月经周期的生物活性与免疫反应性比值(B:I)范围为1.4 - 3.4,平均值为2.5。卵泡早期、卵泡晚期、排卵前高峰和黄体期的比值分别为2.7、2.3、1.4和2.6。生物测定法和放射免疫分析法(RIA)获得的血清FSH值的相关系数(r)为0.91。还对以下各类患者的FSH生物活性进行了测量,其平均值如下:口服避孕药使用者(未检测到)、下丘脑性闭经(18.7 mIU/ml;B:I,2.6)、卵巢早衰(163 mIU/ml;B:I,1.7)和绝经后女性(191 mIU/ml;B:I,1.6)。这些发现表明,测量免疫反应性FSH水平能够正确反映处于月经周期的女性以及某些性腺功能亢进和减退状态患者血清中FSH的生物活性。颗粒细胞芳香化酶生物测定法是未来在生理和病理生理条件下评估生物活性FSH的一种新工具。