Hand T H, Marek G J, Seiden L S
University of Chicago, Department of Pharmacological and Physiological Sciences, IL 60637.
Psychopharmacology (Berl). 1991;105(4):453-8. doi: 10.1007/BF02244363.
The behavioral effects of racemic mianserin, its (+) and (-) enantiomers, and its metabolites desmethylmianserin and 8-hydroxymianserin were evaluated on the differential-reinforcement-of-low-rate 72-s (DRL 72-s) schedule, a screen known to be sensitive to and specific for the antidepressant properties of drugs. Racemic mianserin produced the antidepressant-like effect (increased reinforcement rate, decreased response rate) at 5 and 10 mg/kg. The mianserin enantiomers showed the antidepressant-like effect beginning at lower doses [(+) mianserin; 0.6 mg/kg; (-) mianserin: 2.5 mg/kg]. The mianserin metabolites showed no clear dose-related effect at doses up to 10 mg/kg. It is concluded that the antidepressant-like effects of mianserin are due to the activity of the parent compound rather than to its metabolites, and that they may be primarily attributable to the (+) enantiomer. The greater potency of (+)-mianserin may be related to its higher affinity for the 5-HT2 receptor.
在低速率72秒差别强化程序(DRL 72-s)下评估了消旋米安色林及其(+)和(-)对映体以及其代谢产物去甲米安色林和8-羟基米安色林的行为效应,该程序是一种已知对药物抗抑郁特性敏感且具有特异性的筛选方法。消旋米安色林在5和10mg/kg剂量时产生了类抗抑郁作用(强化率增加,反应率降低)。米安色林对映体在较低剂量时就开始显示出类抗抑郁作用[(+)米安色林;0.6mg/kg;(-)米安色林:2.5mg/kg]。米安色林代谢产物在高达10mg/kg的剂量下未显示出明显的剂量相关效应。得出的结论是,米安色林的类抗抑郁作用归因于母体化合物的活性而非其代谢产物,并且这些作用可能主要归因于(+)对映体。(+)-米安色林更强的效力可能与其对5-HT2受体更高的亲和力有关。