Stancheva S L, Alova L G
Farmakol Toksikol. 1988 May-Jun;51(3):16-8.
In vitro studies of effects of some nootropic drugs (centrophenoxine, piracetam and aniracetam) on monoamine oxidase (MAO) activity in the rat striatum and hypothalamus, using tyramine, serotonin and beta-phenylethylamine as substrates, were carried out. At all concentrations used (5.10(-5)-1.10(-3) M) centrophenoxine inhibited total MAO, MAO A and MAO B in both brain structures. Piracetam activated striatal and hypothalamic total MAO, hypothalamic MAO A and MAO B but exerted a pronounced inhibitory effect on MAO A and MAO B activity in the striatum. Aniracetam inhibited total MAO and MAO A in both brain structures but activated striatal and hypothalamic MAO B. The different effects of centrophenoxine, piracetam and aniracetam on MAO activity in the brain structures support the view for the independent mode of action of nootropic drugs in spite of their similar molecular and metabolic activity.
利用酪胺、血清素和β-苯乙胺作为底物,对某些促智药(氯酯醒、吡拉西坦和阿尼西坦)对大鼠纹状体和下丘脑单胺氧化酶(MAO)活性的体外作用进行了研究。在所使用的所有浓度(5×10⁻⁵ - 1×10⁻³ M)下,氯酯醒均抑制了这两个脑区结构中的总MAO、MAO A和MAO B。吡拉西坦激活了纹状体和下丘脑的总MAO、下丘脑的MAO A和MAO B,但对纹状体中的MAO A和MAO B活性产生了显著抑制作用。阿尼西坦抑制了这两个脑区结构中的总MAO和MAO A,但激活了纹状体和下丘脑的MAO B。氯酯醒、吡拉西坦和阿尼西坦对脑区结构中MAO活性的不同影响支持了促智药尽管具有相似的分子和代谢活性但作用方式独立的观点。