Takeda K, Uchiumi F, Takita M, Kato T
Department of Life Chemistry, Graduate School at Nagatsuta, Tokyo Institute of Technology, Yokohama 227, Japan.
Neurochem Int. 1989;15(1):55-60. doi: 10.1016/0197-0186(89)90076-4.
A rapid and sensitive enzyme immunoassay (EIA) for cholecystokinin octapeptide sulfate (CCK-8S) has been developed. The assay is based on a double antibody method using N-terminal specific antibody to CCK-8S, and CCK-8S conjugated with horseradish peroxidase as the enzyme labeled antigen. The time for the first incubation was 2 h. The time for the second incubation, during which the first antibody was precipitated using the second antibody which contained polyethylene glycol 6000 as an accelerator of the immune reaction, was 5 min. The total assay time was less than 3 h. Intra- and interassay coefficients of variation were 4.4-5.8 and 2.7-10.97%, respectively. The minimal detectable dose was 2 pg of CCK-8S in this assay. To demonstrate the utility of this EIA, we applied this assay to evaluate changes in the levels of CCK-8S immunoreactivity in various regions of the brain after kainic acid-induced seizures in the rat. This treatment decreased the contents of CCK-8S immunoreactivity in the frontal cortex, amygdala and hippocampus. These data show that this EIA system is rapid and sensitive enough to measure changes in the tissue levels of CCK-8S.
已开发出一种用于硫酸缩胆囊素八肽(CCK - 8S)的快速灵敏的酶免疫测定法(EIA)。该测定法基于双抗体法,使用针对CCK - 8S的N端特异性抗体,以及与辣根过氧化物酶偶联的CCK - 8S作为酶标记抗原。第一次孵育时间为2小时。第二次孵育时间为5分钟,在此期间使用含有聚乙二醇6000作为免疫反应促进剂的第二抗体沉淀第一抗体。总测定时间少于3小时。批内和批间变异系数分别为4.4 - 5.8%和2.7 - 10.97%。该测定法的最小可检测剂量为2 pg CCK - 8S。为了证明这种EIA的实用性,我们应用该测定法评估了大鼠在 kainic 酸诱导癫痫发作后大脑各个区域中CCK - 8S免疫反应性水平的变化。这种处理降低了额叶皮质、杏仁核和海马体中CCK - 8S免疫反应性的含量。这些数据表明,这种EIA系统快速且灵敏,足以测量组织中CCK - 8S水平的变化。