Lindahl J
Scand J Clin Lab Invest. 1980;40(8):783-93. doi: 10.3109/00365518009095596.
The endogenous production of 14CO during the first week after administration of 2-[14C]glycine, i.e. the early peak of 14CO derived mainly from erythropoietic and hepatic haem turnover, was measured in six normal subjects. Samples from the body CO store were collected by washout of CO with oxygen breathing, CO concentration of expired gas was determined with an infrared CO-meter and, for determination of 14C activity, CO washed out was oxidized to CO2 in a trapping system and absorbed in ethanolamine. The endogenous production of CO was measured with a rebreathing technique and the production of 14CO was calculated. The specific activity and total amount of circulating red cell haemoglobin haem was determined to calculate the potential late peak of 14CO production. The method for determination of 14CO expired was demonstrated to be specific and reproducible and no haemolysis induced by the sampling procedure was detected. The average production of 14CO was 6.94 nCi/24 h the day after injection of 100 muCi of labelled glycine and decreased gradually to 1.08 nCi/24 h on day 8. The early labelled peak was 32.9 +/0 8.1 nCi (mean +/- SD) and the potential late labelled peak 221 +/- 30 nCi. The early peak represented 13.0 +/- 2.9% of the calculated total production of labelled CO, a figure significantly lower than erythropoietic and hepatic haem turnover calculated from total bilirubin or CO production and red cell life span, probably due to the hepatic component being underestimated by the radiolabelled precursor method.
在六名正常受试者中,测定了给予2-[¹⁴C]甘氨酸后第一周内¹⁴CO的内源性生成,即主要源自红细胞生成和肝脏血红素周转的¹⁴CO的早期峰值。通过用氧气呼吸冲洗出CO来收集来自体内CO储存的样本,用红外CO测定仪测定呼出气体中的CO浓度,并且为了测定¹⁴C活性,将冲洗出的CO在捕获系统中氧化为CO₂并吸收到乙醇胺中。用重复呼吸技术测定CO的内源性生成并计算¹⁴CO的生成量。测定循环红细胞血红蛋白血红素的比活性和总量以计算¹⁴CO生成的潜在晚期峰值。已证明测定呼出¹⁴CO的方法具有特异性和可重复性,并且未检测到采样过程引起的溶血。注射100μCi标记甘氨酸后的第二天,¹⁴CO的平均生成量为6.94nCi/24小时,并在第8天逐渐降至1.08nCi/24小时。早期标记峰值为32.9±8.1nCi(平均值±标准差),潜在晚期标记峰值为221±30nCi。早期峰值占计算出的标记CO总生成量的13.0±2.9%,该数值明显低于根据总胆红素或CO生成量以及红细胞寿命计算出的红细胞生成和肝脏血红素周转量,这可能是由于放射性标记前体法低估了肝脏成分。