Dingemanse J, Berlin I, Payan C, Thiede H M, Puech A J
Department of Clinical Pharmacology, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Psychopharmacology (Berl). 1992;106 Suppl:S68-70. doi: 10.1007/BF02246239.
The effects of moclobemide and toloxatone, two reversible monoamine oxidase-A inhibitors, on biochemical parameters that reflect monoamine metabolism and on psychomotor performance parameters were investigated in a study in 12 healthy volunteers. Treatments were given double-blind in a randomized, placebo-controlled cross-over design, with 1 week wash-out between the treatments. Drugs were given thrice daily in the following doses: moclobemide 150-150-150 mg and toloxatone 400-200-400 mg. All assessments were performed on day 8 under standardized conditions. There was no difference with regard to adverse events between moclobemide and toloxatone: both drugs induced a slight decrease in both supine and standing heart rate. Judged on the basis of the area under the curve, the two MAO-inhibitors reduced the plasma levels of DHPG and HVA, with more pronounced effects for moclobemide than for toloxatone. After moclobemide MAO-A inhibition was almost constant over 24 h, whereas the effect of toloxatone was short lasting after each dose. The same differences were reflected in plasma 5-HIAA concentrations and urinary excretion of 3-methoxytyramine and normetanephine. Neither of the compounds tested had any influence on the memory, vigilance, mood, or sleeping habits of the subjects.
在一项针对12名健康志愿者的研究中,调查了两种可逆性单胺氧化酶-A抑制剂吗氯贝胺和托洛沙酮对反映单胺代谢的生化参数以及对精神运动性能参数的影响。治疗采用随机、安慰剂对照的交叉双盲设计,治疗之间有1周的洗脱期。药物每日三次给药,剂量如下:吗氯贝胺150 - 150 - 150毫克,托洛沙酮400 - 200 - 400毫克。所有评估均在第8天的标准化条件下进行。吗氯贝胺和托洛沙酮在不良事件方面没有差异:两种药物均导致仰卧和站立心率略有下降。根据曲线下面积判断,两种单胺氧化酶抑制剂均降低了二羟基苯乙酸(DHPG)和高香草酸(HVA)的血浆水平,吗氯贝胺的作用比托洛沙酮更明显。服用吗氯贝胺后,单胺氧化酶-A的抑制作用在24小时内几乎保持恒定,而托洛沙酮的作用在每次给药后持续时间较短。血浆5-羟吲哚乙酸(5-HIAA)浓度以及3-甲氧基酪胺和去甲变肾上腺素的尿排泄也反映出相同的差异。所测试的两种化合物均对受试者的记忆、警觉性、情绪或睡眠习惯没有任何影响。