Brown P S, Sharpe R M, Hartog M, Shahmanesh M
Acta Endocrinol (Copenh). 1976 Aug;82(4):673-82. doi: 10.1530/acta.0.0820673.
The assay of FSH by a radioligand receptor assay (RLA) using homogenates of rat testicular tissue incubated for 17 h at 21 degrees C has been assessed. Chloramine-T or lactoperoxidase were used for iodination. The assay gave linear dose-response lines between 30 and 2000 ng sheep FSH/tube, and there was usually no major interference by LH. Two batches of labelled FSH, however, gave assays in which LH showed a striking interaction with FSH. When these batches were avoided and FSH and LH were mixed in ratios that differed less than fourfold, the assay was combined successfully, in the same tubes, with an RLA for LH, using LH and FSH labelled with 131I and 125I respectively. The RLA for FSH was not suitable for assay of FSH in rat serum because of apparent non-specific interference. Assay by RLA of rat FSH, in pituitary homogenates or released during incubation in vitro, gave results which were not closely correlated with those of either conventional bioassay or radioimmunoassay.
已评估了使用在21摄氏度下孵育17小时的大鼠睾丸组织匀浆,通过放射性配体受体分析(RLA)来测定促卵泡激素(FSH)。使用氯胺-T或乳过氧化物酶进行碘化。该分析在每管30至2000纳克绵羊FSH之间给出了线性剂量反应线,并且通常促黄体生成素(LH)没有重大干扰。然而,两批标记的FSH进行的分析中,LH与FSH表现出显著的相互作用。当避免使用这些批次,并且FSH和LH以相差小于四倍的比例混合时,该分析在同一管中成功地与使用分别用131I和125I标记的LH和FSH的LH的RLA相结合。由于明显的非特异性干扰,FSH的RLA不适合用于测定大鼠血清中的FSH。通过RLA对垂体匀浆中或体外孵育期间释放的大鼠FSH进行分析,得到的结果与传统生物测定法或放射免疫测定法的结果均无密切相关性。