Dyck L E
Brain Res Bull. 1984 Jan;12(1):23-8. doi: 10.1016/0361-9230(84)90210-7.
Intraperitoneal administration of phenelzine (PLZ) or of beta-phenylethylamine (PE) quickly leads to short periods of behavioural activation, which are primarily dopaminergic and serotonergic in nature, respectively. In order to determine whether these behavioural effects are due to PLZ- or PE-induced displacement of dopamine (DA) or serotonin (5HT), the ability of these compounds to stimulate release of radiolabelled DA and 5HT from slices of rat striatum was assessed. Additionally, at various times following IP administration of behaviourally active doses of PLZ or PE to rats, the striatal levels of the drugs were measured. Both PLZ and PE were able to stimulate a greater release of radiolabelled DA than of 5HT. Lower concentrations of PE (0.8, 8.0 microM) than of PLZ (100 microM, 1 mM) stimulated release. The striatal levels (approximately 200 microM) of PLZ, as well as of PE, attained at times corresponding to behavioural activation seemed sufficient to cause release of both DA and 5HT. It was concluded, therefore, that the mode of action of these compounds may involve displacement, or release, of these biogenic amines, though it is not clear how such release ultimately leads to the behaviours observed.
腹腔注射苯乙肼(PLZ)或β-苯乙胺(PE)会迅速导致短时间的行为激活,其本质上分别主要是多巴胺能和5-羟色胺能的。为了确定这些行为效应是否是由于PLZ或PE诱导的多巴胺(DA)或5-羟色胺(5HT)的置换,评估了这些化合物刺激大鼠纹状体切片中放射性标记的DA和5HT释放的能力。此外,在对大鼠腹腔注射具有行为活性剂量的PLZ或PE后的不同时间,测量了药物的纹状体水平。PLZ和PE都能刺激放射性标记的DA比5HT有更大的释放。刺激释放的PE浓度(0.8、8.0微摩尔)低于PLZ(100微摩尔、1毫摩尔)。在与行为激活相对应的时间达到的PLZ以及PE的纹状体水平(约200微摩尔)似乎足以引起DA和5HT的释放。因此得出结论,这些化合物的作用方式可能涉及这些生物胺的置换或释放,尽管尚不清楚这种释放最终如何导致所观察到的行为。