Rollag M D, Niswender G D
Endocrinology. 1976 Feb;98(2):482-9. doi: 10.1210/endo-98-2-482.
A specific and sensitive double-antibody radioimmunoassay for melatonin (N-acetyl-5-methoxytryptamine) has been developed utilizing rabbit antisera to a bovine serum albumin conjugate of N-succinyl-5-methoxytryptamine and utilizing N-3-(4-hydroxyphenl)-propionyl-5-methoxytryptamine for radioiodination. The least detectable concentration of melatonin standard was 10 pmolar (2.3 pg/tube) with 50% inhibition resultinhibition curves obtained with increasing quantities of melatonin or increasing quantities of chloroform extracts of ovine sera were parallel. The immunoreactivity found in ovine sera c-migrated with [3H]melatonin on silica gel G when developed with chloroform:methanol (9:1). N-Acetylserotonin, 5-methoxytryptamine, serotonin, tryptophan, 6-hydroxymelatonin, 6-methoxytetrahydroharmalan, and several other indole and beta-carboline compounds do not influence the estimation of melatonin in the radioimmunoassay. Concentrations of melatonin could be accurately determined when 31 to 1000 pg were added to 1 ml ovine serum. Serum samples with melatonin concentrations of 1000 pg/ml, 500 pg/ml and 75 pg/ml had intra-assay coefficients of variation of 9.1%, 8.6%, and 17.4%, respectively. The respective inter-assay coefficients of variation were 22.7%, 18.1%, and 37.1%. Ewes exposed to a 12 h light: 12 h dark lighting regimen demonstrated a circadian rhythm in serum concentrations of melatonin. Concentrations ranged from 10-30 pg/ml during periods of light to 100-300 pg/ml during periods of dark. During exposure to continuous light, the circadian rhythm was abolished and concentrations of melatonin were maintained at 10-50 pg/ml. When exposed to conditions of continuous dark the circadian rhythm persisted. A precipitous drop in serum concentrations of melatonin resulted when ewes experiencing peak melatonin concentrations were exposed to light. Concentrations returned to peak levels when the lights were turned off 3.5 h later.
已开发出一种用于褪黑素(N - 乙酰 - 5 - 甲氧基色胺)的特异性和灵敏性双抗体放射免疫测定法,该方法利用兔抗血清针对N - 琥珀酰 - 5 - 甲氧基色胺与牛血清白蛋白的偶联物,并利用N - 3 -(4 - 羟基苯基) - 丙酰 - 5 - 甲氧基色胺进行放射性碘化。褪黑素标准品的最低可检测浓度为10皮摩尔(2.3皮克/管),50%抑制时得到的抑制曲线与褪黑素量增加或绵羊血清氯仿提取物量增加时获得的抑制曲线平行。当用氯仿:甲醇(9:1)展开时,在硅胶G上绵羊血清中发现的免疫反应性与[³H]褪黑素共迁移。N - 乙酰血清素、5 - 甲氧基色胺、血清素、色氨酸、6 - 羟基褪黑素、6 - 甲氧基四氢哈尔满以及其他几种吲哚和β - 咔啉化合物在放射免疫测定中不影响褪黑素的测定。当向1毫升绵羊血清中添加31至1000皮克时,褪黑素浓度可准确测定。褪黑素浓度为1000皮克/毫升、500皮克/毫升和75皮克/毫升的血清样本的批内变异系数分别为9.1%、8.6%和17.4%。相应的批间变异系数分别为22.7%、18.1%和37.1%。暴露于12小时光照:12小时黑暗光照方案的母羊血清褪黑素浓度呈现昼夜节律。光照期间浓度范围为10 - 30皮克/毫升,黑暗期间为100 - 300皮克/毫升。在持续光照期间,昼夜节律消失,褪黑素浓度维持在10 - 50皮克/毫升。当暴露于持续黑暗条件下时,昼夜节律持续存在。经历褪黑素浓度峰值的母羊暴露于光照下时,血清褪黑素浓度急剧下降。3.5小时后关灯时,浓度恢复到峰值水平。