Campbell W, Clark M S, Mitchell P J, Needham P L, Semple J M
Psychopharmacology (Berl). 1986;89(2):208-15. doi: 10.1007/BF00310631.
BRL 20596 (N-(4-amino-5-chloro-2-methoxyphenyl)-1-phenylmethyl-4-piperidine-carbox amide) is a novel anilide related to clebopride (a gastric prokinetic benzamide) in which the sole change is reversal of the amide bond. Previous studies have shown conformational and electronic differences between these molecules which result in the anilide losing its gastric prokinetic activity, whilst retaining its central nervous system activity. Pharmacological and biochemical properties of BRL 20596 are compared here in animals with chlorpromazine, clebopride, haloperidol and sulpiride. BRL 20596 potently inhibited a number of behaviours, such as conditioned avoidance, amphetamine-induced stereotypy and turning, and apomorphine-induced climbing. Homovanillic acid (HVA) levels in the striatum and nucleus accumbens were raised at similar dose levels to those which inhibited these behaviours, whilst sedative activity was only exhibited at much higher dose levels. Haemodynamic changes were only observed with high IV doses of BRL 20596. Much lower doses of sulpiride were needed to raise prolactin levels than to raise HVA levels. This was not the case with BRL 20596 and the other drugs, where the doses needed for the two effects were similar. The results suggest that BRL 20596 is a central dopamine antagonist, with low sedative and haemodynamic activity.
BRL 20596(N-(4-氨基-5-氯-2-甲氧基苯基)-1-苯基甲基-4-哌啶甲酰胺)是一种与氯波必利(一种促胃动力苯甲酰胺)相关的新型酰苯胺,唯一的变化是酰胺键的反转。先前的研究表明,这些分子之间存在构象和电子差异,这导致酰苯胺失去其促胃动力活性,同时保留其中枢神经系统活性。本文在动物中将BRL 20596的药理和生化特性与氯丙嗪、氯波必利、氟哌啶醇和舒必利进行了比较。BRL 20596能有效抑制多种行为,如条件性回避、苯丙胺诱导的刻板行为和旋转以及阿扑吗啡诱导的攀爬。纹状体和伏隔核中的高香草酸(HVA)水平在与抑制这些行为相似的剂量水平下升高,而镇静活性仅在高得多的剂量水平下表现出来。仅在静脉注射高剂量的BRL 20596时才观察到血流动力学变化。与升高HVA水平相比,升高催乳素水平所需的舒必利剂量要低得多。而BRL 20596和其他药物并非如此,这两种效应所需的剂量相似。结果表明,BRL 20596是一种中枢多巴胺拮抗剂,具有低镇静和血流动力学活性。