Dattani M T, Winrow A P, Tuil'Pakov A, Pringle P J, Hindmarsh P C, Brook C G, Marshall N J
Endocrine Unit, Middlesex Hospital, London, UK.
Eur J Endocrinol. 1996 Jul;135(1):87-95. doi: 10.1530/eje.0.1350087.
We compared the immunoactivity of human growth hormone (hGH) with its bioactivity after stimulation of hGH release into the circulation by the administration of growth hormone-releasing hormone [GHRH(1-29)-NH2] according to a pre-determined protocol to four normal adult volunteers. We used the Hybritech immunoradiometric assay to measure the immunoactive GH concentrations. Bioactive GH concentrations were measured using the highly quantitative and precise eluted stain bioassay system (ESTA). The high sample capacity of the ESTA bioassay permitted us to monitor the bioactivities in closely timed sequential samples, and in far greater detail than has previously been possible. Two pulses of GHRH(1-29)-NH2 were administered intravenously to the four adult male volunteers (aged 24-37 years) on a weekly basis over a 4-week period. Two different doses of GHRH(1-29)-NH2 (0.1 and 1.0 micrograms/kg) were tested. These were separated by specified time intervals (60 or 120 min). Responses in the four individuals were variable. However, although the immuno- and bioactivities generally agreed well, there was a systematic and progressive increase in the bioactivity/immunoactivity (B/I) ratios as half of the response peaks were approached. After these peak concentrations, the B/I ratios subsequently returned to values that were close to unity. The enhanced bioactivity of the peak samples from the two volunteers in whom the largest magnitudes of response were observed was found to be labile after long-term storage at -20 degrees C. We suggest that the preferential rise in GH bioactivity, as opposed to immunoactivity, in response to GHRH(1-29)-NH2 was due to progressive changes in the concentrations of isoforms of GH that are not detectable in the Hybritech immunoassay.
我们按照预先确定的方案,对四名正常成年志愿者施用生长激素释放激素[GHRH(1 - 29)-NH₂]以刺激人类生长激素(hGH)释放进入循环系统,之后比较了hGH的免疫活性与其生物活性。我们使用Hybritech免疫放射分析来测量免疫活性GH浓度。生物活性GH浓度通过高度定量且精确的洗脱染色生物测定系统(ESTA)进行测量。ESTA生物测定的高样本容量使我们能够监测紧密定时的连续样本中的生物活性,且细节程度远超以往。在4周时间内,每周对四名成年男性志愿者(年龄24 - 37岁)静脉注射两次GHRH(1 - 29)-NH₂。测试了两种不同剂量的GHRH(1 - 29)-NH₂(0.1和1.0微克/千克)。它们被特定的时间间隔(60或120分钟)隔开。这四名个体的反应各不相同。然而,尽管免疫活性和生物活性总体上吻合良好,但随着接近反应峰值的一半,生物活性/免疫活性(B/I)比值出现系统性且渐进性的增加。在这些峰值浓度之后,B/I比值随后恢复到接近1的值。在观察到最大反应幅度的两名志愿者的峰值样本中,增强的生物活性在-20℃长期储存后被发现不稳定。我们认为,与免疫活性相比,响应GHRH(1 - 29)-NH₂时GH生物活性的优先升高是由于Hybritech免疫测定中无法检测到的GH异构体浓度的渐进性变化所致。