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生长激素缺乏儿童接受脉冲式注射生长激素释放激素1 - 40后血浆免疫反应性生长激素释放激素和血清生长激素浓度

Plasma immunoreactive GHRH and serum GH concentrations following pulsatile GHRH 1-40 administration in GH deficient children.

作者信息

Smith P J, Pringle P J, Brook C G, Schulster D, Rafferty B

机构信息

Endocrine Unit, Middlesex Hospital, London, UK.

出版信息

Clin Endocrinol (Oxf). 1987 Oct;27(4):501-7. doi: 10.1111/j.1365-2265.1987.tb01179.x.

Abstract

We have studied the clearance from plasma of immunoreactive growth hormone releasing hormone 1-40 (IR-GHRH) following intravenous (i.v.) and subcutaneous (s.c.) administration and the relationship between exogenous plasma IR-GHRH concentrations and GH secretion in five GH insufficient children receiving long term nocturnal pulsatile GHRH 1-40. The i.v. studies with GHRH 1-40 1 micrograms/kg demonstrated a distribution half life (t1/2) of 3.9 (SD 0.9) min and an elimination t1/2 of 53.1 (SD 3.2) min. In the s.c. studies the elimination phase was similar to the i.v. results but the transit time to the GHRH peak was slower than the i.v. distribution t1/2 9.9 (SD 3.6) min. These characteristics were maintained during successive pulses of subcutaneous GHRH. The mean IR-GHRH peaks following s.c. GHRH 1-40 administration of 1 microgram/kg and 2 micrograms/kg were 37- and 18-fold lower respectively than the mean IR-GHRH peak observed after the i.v. 1 microgram/kg bolus study. A significant correlation was shown between peak plasma IR-GHRH and serum GH concentrations during the s.c. (r = 0.75) but not the i.v. studies. Pulsatile GHRH administration has been shown to stimulate GH secretion and growth acceleration in GH insufficient children. Knowledge of the relationship between GHRH 1-40 absorption from the subcutaneous site and GH secretion is important for the development of an optimal GHRH treatment regimen in GH insufficient children.

摘要

我们研究了5名长期接受夜间脉冲式生长激素释放激素1-40(GHRH 1-40)治疗的生长激素缺乏儿童静脉注射(i.v.)和皮下注射(s.c.)免疫反应性生长激素释放激素1-40(IR-GHRH)后从血浆中的清除情况,以及外源性血浆IR-GHRH浓度与生长激素(GH)分泌之间的关系。静脉注射1微克/千克GHRH 1-40的研究显示,分布半衰期(t1/2)为3.9(标准差0.9)分钟,消除半衰期为53.1(标准差3.2)分钟。在皮下注射研究中,消除阶段与静脉注射结果相似,但达到GHRH峰值的转运时间比静脉注射分布半衰期慢,为9.9(标准差3.6)分钟。在连续皮下注射GHRH脉冲期间,这些特征得以保持。皮下注射1微克/千克和2微克/千克GHRH 1-40后,平均IR-GHRH峰值分别比静脉注射1微克/千克推注研究后观察到的平均IR-GHRH峰值低37倍和18倍。皮下注射研究中,血浆IR-GHRH峰值与血清GH浓度之间显示出显著相关性(r = 0.75),但静脉注射研究中未显示出相关性。脉冲式GHRH给药已被证明可刺激生长激素缺乏儿童的GH分泌和生长加速。了解皮下部位GHRH 1-40吸收与GH分泌之间的关系对于制定生长激素缺乏儿童的最佳GHRH治疗方案很重要。

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