Sieber C, Gnädinger M, Del Pozo E, Shaw S, Weidmann P
Experimental Therapeutics Department, Sandoz Ltd, Basle, Switzerland.
Clin Endocrinol (Oxf). 1988 Jan;28(1):25-32. doi: 10.1111/j.1365-2265.1988.tb01199.x.
The effects of a new somatostatin analogue SMS 201-995 (H-D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr(ol), Sandostatin) on the orthostatic stimulation of plasma renin activity (PRA) following head-up tilting and on angiotensin II (Ang-II) induced aldosterone (PA) release were studied under placebo controlled conditions in separate groups of healthy volunteers consisting of six and 10 subjects, respectively. Head-up tilting (by 60 degrees) produced the characteristic increases in PRA and PA. Administration of SMS 201-995 significantly (P less than 0.05) inhibited this PRA elevation from 30 min on. Throughout the study period, PA levels were not consistently altered by this analogue. Furthermore, SMS 201-995 failed to inhibit the stimulation of PA secretion induced by exogenous angiotensin-II (2-10 ng/kg/min). Results presented here are at variance with data collected with natural somatostatin showing an inhibitory effect on stimulated PA. This discrepancy can be explained by the recently described absence of SMS 201-995 binding sites in primate adrenal cortex and in human aldosteronomas.
在安慰剂对照条件下,分别在由6名和10名受试者组成的健康志愿者不同组中,研究了一种新的生长抑素类似物SMS 201 - 995(H-D-苯丙氨酸-半胱氨酸-苯丙氨酸-D-色氨酸-赖氨酸-苏氨酸-半胱氨酸-苏氨酸(醇),善宁)对抬头倾斜后血浆肾素活性(PRA)的直立刺激作用以及对血管紧张素II(Ang-II)诱导的醛固酮(PA)释放的影响。抬头倾斜(60度)使PRA和PA出现特征性升高。从30分钟起,给予SMS 201 - 995显著(P小于0.05)抑制了这种PRA升高。在整个研究期间,该类似物未使PA水平持续改变。此外,SMS 201 - 995未能抑制外源性血管紧张素II(2 - 10 ng/kg/分钟)诱导的PA分泌刺激。此处呈现的结果与天然生长抑素收集的数据不同,天然生长抑素对刺激的PA有抑制作用。这种差异可以通过最近描述的在灵长类动物肾上腺皮质和人醛固酮瘤中不存在SMS 201 - 995结合位点来解释。