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艾迪生病中急性升高的促肾上腺皮质激素水平与外周血浆中精氨酸加压素和促肾上腺皮质激素释放因子浓度升高无关。

Acutely raised corticotropin levels in Addison's disease are not associated with increased plasma arginine vasopressin and corticotropin-releasing factor concentrations in peripheral plasma.

作者信息

Wittert G A, Livesey J H, Florkowski C, Or H K, Donald R A, Espiner E A

机构信息

Department of Endocrinology, Princess Margaret Hospital, Christchurch, New Zealand.

出版信息

J Clin Endocrinol Metab. 1993 Jan;76(1):192-6. doi: 10.1210/jcem.76.1.8380605.

Abstract

Using an intensive sampling protocol we have examined the associations of peripheral plasma arginine vasopressin (AVP) and CRF with nocturnal ACTH hypersecretion in patients with Addison's disease. Six subjects were studied during a phase of cortisol withdrawal (36 h) and after cortisol substitution, and the findings were compared to those in four normal control subjects. The pulse properties of ACTH hypersecretion at a 10-min sampling interval have also been examined in these settings, using Cluster analysis. In the period before cortisol replacement, the Addison's patients showed significantly greater ACTH peak maxima and peak increments than the control subjects [107 +/- 44 vs. 5.5 +/- 1.3 pmol/L (P = 0.009) and 57 +/- 23 pmol/L vs. 3.7 +/- 0.9 pmol/L (P < 0.05), respectively]. After cortisol replacement, a significant decrease in mean peak increment (57 +/- 24 vs. 15 +/- 5 pmol/L; P = 0.021) occurred. The mean interpulse intervals did not differ significantly between the Addison's and control subjects (59 +/- 5 vs. 59 +/- 4 min overall). Although not significant, the trend for the pulse interval to increase after oral cortisol (60 +/- 6 vs. 72 +/- 9 min) is probably a result of the extremely low levels of ACTH after oral cortisol administration, making peak detection difficult. Despite the ACTH hypersecretion in the Addison's subjects, plasma AVP levels were at no time different from those in the control subjects. Plasma CRF levels tended to be lower in the Addison's patients than in the control subjects. We conclude that in states of cortisol deficiency, such as Addison's disease, ACTH hypersecretion results from enhanced ACTH peak amplitude, without a change in the frequency of ACTH secretory pulses. The marked increase in plasma ACTH that follows acute cortisol deprivation is independent of detectable changes in peripheral plasma levels of CRF or AVP.

摘要

我们采用强化采样方案,研究了艾迪生病患者外周血浆精氨酸加压素(AVP)和促肾上腺皮质激素释放因子(CRF)与夜间促肾上腺皮质激素(ACTH)分泌过多之间的关联。对6名受试者在皮质醇撤药阶段(36小时)及皮质醇替代治疗后进行了研究,并将结果与4名正常对照受试者的结果进行比较。在这些情况下,还使用聚类分析研究了以10分钟采样间隔的ACTH分泌过多的脉冲特性。在皮质醇替代治疗前,艾迪生病患者的ACTH峰值最大值和峰值增量显著高于对照受试者[分别为107±44与5.5±1.3 pmol/L(P = 0.009)和57±23 pmol/L与3.7±0.9 pmol/L(P < 0.05)]。皮质醇替代治疗后,平均峰值增量显著下降(57±24与15±5 pmol/L;P = 0.021)。艾迪生病患者与对照受试者的平均脉冲间期无显著差异(总体上分别为59±5与59±4分钟)。口服皮质醇后脉冲间期虽无显著增加趋势(60±6与72±9分钟),但可能是由于口服皮质醇后ACTH水平极低,难以检测到峰值。尽管艾迪生病患者存在ACTH分泌过多,但血浆AVP水平在任何时候都与对照受试者无异。艾迪生病患者的血浆CRF水平往往低于对照受试者。我们得出结论,在皮质醇缺乏状态下,如艾迪生病,ACTH分泌过多是由于ACTH峰值幅度增加,而ACTH分泌脉冲频率无变化。急性皮质醇缺乏后血浆ACTH的显著增加与外周血浆CRF或AVP水平的可检测变化无关。

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