de Mey C, Enterling D, Hansen-Schmidt S, Meineke I
SK&F-Institute for Applied Clinical Pharmacology, Goettingen, F.R.G.
J Cardiovasc Pharmacol. 1989 Jan;13(1):25-31.
SK&F 86466 is a novel alpha-adrenoceptor blocking drug shown in preclinical profiling to have relative selectivity for the pre- and postjunctional alpha 2-adrenoreceptor. In the present clinical study, the effects of single oral doses of 10, 25, and 50 mg SK&F 86466 on supine and stimulated circulatory and neuroendocrine function were assessed in eight normal subjects studied in a placebo-controlled balanced cross-over design with the drugs administered in double-blind fashion. SK&F 86466 caused a dose-related increase in stimulated (postural and cold challenge) and supine plasma norepinephrine (NE) concentrations. This increase was associated with an increase in supine heart rate (HR) and plasma renin activity and orthostatically stimulated HR, with little increase in systolic blood pressure (SBP) and no increase in diastolic blood pressure (DBP). Assuming that no changes occurred in catecholamine clearance, SK&F 86466 thus appeared to have a prejunctional alpha 2-adrenoreceptor blocking effect, which was countered by a post-junctional alpha-adrenoreceptor blocking effect at the level of the resistance vessels, whereas this latter effect did not alter the pressor responses to cold and postural challenge.
SK&F 86466是一种新型α-肾上腺素能受体阻断药物,临床前研究表明其对节前和节后α2-肾上腺素能受体具有相对选择性。在本临床研究中,采用安慰剂对照、平衡交叉设计,对8名正常受试者进行双盲给药,评估单次口服10、25和50mg SK&F 86466对仰卧位及刺激状态下循环和神经内分泌功能的影响。SK&F 86466导致刺激状态(体位改变和冷刺激)及仰卧位血浆去甲肾上腺素(NE)浓度呈剂量依赖性增加。这种增加与仰卧位心率(HR)、血浆肾素活性升高以及体位性刺激心率升高有关,收缩压(SBP)升高幅度较小,舒张压(DBP)无升高。假设儿茶酚胺清除率无变化,因此SK&F 86466似乎具有节前α2-肾上腺素能受体阻断作用,而在阻力血管水平被节后α-肾上腺素能受体阻断作用所抵消,而后一种作用并未改变对冷刺激和体位改变的升压反应。