Morgan L M, Morris B A, Marks V
Ann Clin Biochem. 1978 May;15(3):172-7. doi: 10.1177/000456327801500138.
A radioimmunoassay for the measurement of gastric inhibitory polypeptide (GIP) in unextracted plasma in man has been developed using a rabbit antiserum raised against porcine GIP. Porcine GIP was employed also as standard and to produce a 125I-labelled tracer. The assay was able to distinguish 110 pg/ml GIP from zero in plasma samples. Negligible cross-reactivity was demonstrated with cholecystokinin, insulin, pancreatic polypeptide, glucagon, secretin, and vasoactive intestinal polypeptide. The mean overnight fasting plasma GIP level in 28 normal subjects was 203 pg/ml (range: undetectable--420 pg/ml). Plasma GIP levels rose, within 45 minutes of eating a mixed meal, to a mean level of 1573 pg/ml.
已开发出一种利用针对猪胃抑制多肽(GIP)产生的兔抗血清来测量人未提取血浆中GIP的放射免疫分析法。猪GIP也用作标准品并用于制备125I标记的示踪剂。该分析方法能够在血浆样本中区分110 pg/ml的GIP和零值。结果表明,该方法与胆囊收缩素、胰岛素、胰多肽、胰高血糖素、促胰液素和血管活性肠肽的交叉反应可忽略不计。28名正常受试者夜间空腹血浆GIP的平均水平为203 pg/ml(范围:未检测到——420 pg/ml)。进食混合餐后45分钟内,血浆GIP水平升至平均1573 pg/ml。