Dickstein G, Shechner C, Nicholson W E, Rosner I, Shen-Orr Z, Adawi F, Lahav M
Division of Endocrinology, Haifa Medical Center, Israel.
J Clin Endocrinol Metab. 1991 Apr;72(4):773-8. doi: 10.1210/jcem-72-4-773.
Adrenal response to iv administration of 1-24 ACTH (250 micrograms) was examined in normal volunteers under various conditions. The effect of basal cortisol levels was examined by performing the tests at 0800 h with and without pretreatment with dexamethasone. The effect of time of day was evaluated by performing the tests at 0800 h and at 1600 h, eliminating possible basal cortisol influence by pretreatment with dexamethasone. In the first set of tests, despite significantly different baseline levels, 30-min cortisol levels were not different (618 +/- 50 vs. 590 +/- 52 nmol/L). Afternoon cortisol levels in response to ACTH were found to be significantly higher than morning levels at 5 min (254 +/- 50 vs. 144 +/- 36 nmol/L, p less than 0.01) and at 15 min (541 +/- 61 vs. 433 +/- 52 nmol/L, p less than 0.02). This difference in response was no longer notable at 30 min (629 +/- 52 and 591 +/- 52 nmol/L). We tried also to determine the lowest ACTH dose which will elicit a maximal cortisol response. No difference was found in cortisol levels at 30 and 60 min in response to 250 and 5 micrograms 1-24 ACTH. Using 1 micrograms ACTH, the 30-min response did not differ from that to 250 micrograms (704 +/- 72 vs. 718 +/- 55 nmol/L, respectively). However, the 60-min response to 1 microgram was significantly lower (549 +/- 61 vs. 842 +/- 110 nmol/L, p less than 0.01). Using this low dose ACTH test (1 microgram, measuring 30-min cortisol level), we were able to develop a much more sensitive ACTH test, which enabled us to differentiate a subgroup of patients on long-term steroid treatment who responded normally to the regular 250 micrograms test, but had a reduced response to 1 microgram. The stability of 1-24 ACTH in saline solution, kept at 4 C, was checked. ACTH was found to be fully stable after 2 hs in a concentration of 5 micrograms/ml in glass tube and 0.5 micrograms/ml in plastic tube. It was also found to be fully stable, both immunologically and biologically, for 4 months, under these conditions. We conclude that the 30-min cortisol response to ACTH is constant, unrelated to basal cortisol level or time of day. It is therefore the best criterion for measuring adrenal response in the short ACTH test. The higher afternoon responses at 5 and 15 min suggest greater adrenal sensitivity in the afternoon, but further studies are needed to clarify this issue.(ABSTRACT TRUNCATED AT 400 WORDS)
在各种条件下,对正常志愿者静脉注射1-24促肾上腺皮质激素(ACTH,250微克)后的肾上腺反应进行了检查。通过在08:00时进行测试,且分别在有和没有地塞米松预处理的情况下,研究基础皮质醇水平的影响。通过在08:00时和16:00时进行测试,并用地塞米松预处理消除可能的基础皮质醇影响,来评估一天中不同时间的影响。在第一组测试中,尽管基线水平有显著差异,但30分钟时的皮质醇水平并无差异(分别为618±50和590±52纳摩尔/升)。发现下午ACTH刺激后的皮质醇水平在5分钟时(254±50对144±36纳摩尔/升,p<0.01)和15分钟时(541±61对433±)显著高于上午水平。这种反应差异在30分钟时不再明显(分别为629±52和591±52纳摩尔/升)。我们还试图确定能引发最大皮质醇反应的最低ACTH剂量。对250微克和5微克1-24ACTH,30分钟和60分钟时的皮质醇水平没有差异。使用1微克ACTH时,30分钟的反应与250微克时无差异(分别为704±72和718±55纳摩尔/升)。然而,1微克时60分钟的反应显著较低(549±61对842±110纳摩尔/升,p<0.01)。使用这种低剂量ACTH测试(1微克,测量30分钟皮质醇水平),我们能够开发出一种更敏感的ACTH测试,使我们能够区分长期接受类固醇治疗的一组患者,他们对常规的250微克测试反应正常,但对1微克的反应降低。检查了1-24ACTH在4℃生理盐水中的稳定性。发现在玻璃管中浓度为5微克/毫升、塑料管中浓度为0.5微克/毫升时,2小时后ACTH完全稳定。在这些条件下,还发现其在免疫和生物学方面4个月内完全稳定。我们得出结论,ACTH刺激后30分钟的皮质醇反应是恒定的,与基础皮质醇水平或一天中的时间无关。因此,它是短时间ACTH测试中测量肾上腺反应的最佳标准。下午5分钟和15分钟时较高的反应表明下午肾上腺敏感性更高,但需要进一步研究来阐明这一问题。(摘要截于400字)