A radioimmunoassay for ovine prolactin is described based on the inhibition of the reaction between (131)I-labelled ovine prolactin and guinea-pig or rabbit antiserum to ovine prolactin. The extent of the reaction after a 4-day incubation period is determined by chromatoelectrophoresis or by adsorption of unchanged (131)I-labelled ovine prolactin on charcoal. The sensitivity is equal to 5.9ng. of prolactin/ml. of plasma with chromatoelectrophoresis, or 0.2ng. of prolactin/ml. of tissue extracts with the charcoal separation. 2. A complete cross-reaction demonstrated between ovine prolactin and caprine pituitary extracts allows the assay to be used to measure caprine prolactin. The partial cross-reactions between ovine prolactin and bovine prolactin and between ovine prolactin and bovine pituitary extract differ, and an alteration in the immunological activity of bovine prolactin during its isolation is suggested. Bovine prolactin in plasma may be measured against a bovine pituitary extract as standard. No cross-reactions were demonstrated with pituitary extracts from a number of other species. The extent of the contamination of ovine and bovine growth hormone preparations by their respective prolactins is shown. 3. Dilutions of ovine and caprine plasma inhibit the reaction between (131)I-labelled ovine prolactin and antiserum with the same characteristics as ovine prolactin. 4. The immunoreactive material in plasma fractionates on Sephadex G-200 and in sucrose density gradients as a single peak similar to that shown by freshly dissolved ovine prolactin. There is no evidence that ovine prolactin is bound to a plasma protein. 5. By suppressing prolactin secretion and assaying serial samples of plasma thereafter it is shown that the immunological activity of the surviving hormone becomes progressively altered with time. It is suggested that this alteration is usually not detected but introduces an element of uncertainty into the quantitative but not the qualitative value of the measurements obtained by reference to standard ovine prolactin.
摘要
本文描述了一种用于检测绵羊催乳素的放射免疫分析方法,该方法基于对(131)I标记的绵羊催乳素与豚鼠或兔抗绵羊催乳素血清之间反应的抑制作用。经过4天孵育期后,反应程度通过色谱电泳或通过将未变化的(131)I标记的绵羊催乳素吸附在活性炭上来确定。采用色谱电泳时,该方法的灵敏度相当于每毫升血浆中5.9纳克催乳素;采用活性炭分离法时,每毫升组织提取物中0.2纳克催乳素。2. 绵羊催乳素与山羊垂体提取物之间呈现完全交叉反应,这使得该检测方法可用于测量山羊催乳素。绵羊催乳素与牛催乳素之间以及绵羊催乳素与牛垂体提取物之间的部分交叉反应有所不同,这表明牛催乳素在分离过程中其免疫活性发生了改变。血浆中的牛催乳素可以以牛垂体提取物作为标准进行检测。未发现与其他多种物种的垂体提取物有交叉反应。文中展示了绵羊和牛生长激素制剂中各自催乳素的污染程度。3. 绵羊和山羊血浆的稀释液抑制(131)I标记的绵羊催乳素与抗血清之间的反应,其特性与绵羊催乳素相同。4. 血浆中的免疫反应性物质在Sephadex G - 200上以及在蔗糖密度梯度中分离为单一峰,类似于新鲜溶解的绵羊催乳素所显示的峰。没有证据表明绵羊催乳素与血浆蛋白结合。5. 通过抑制催乳素分泌并随后检测血浆系列样本,结果表明存活激素的免疫活性随时间逐渐改变。有人认为,这种改变通常未被检测到,但会给通过参照标准绵羊催乳素获得的测量值的定量而非定性值引入不确定性因素。